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<![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a Purchasing Buyer to work for a leading San Diego biotechnology company. Purchasing Buyer This temporary position is independently responsible for the processing of purchase orders for direct (inventory materials) and indirect MRO materials, goods and services to support Customer Orders and Operations as assigned. By analyzing the ERP SAP system, the Buyer will process approved requisitions and issue system generated purchase orders. Where necessary, will process RFQs and negotiate as required to obtain the optimum price from approved suppliers. This position is also responsible for ensuring that purchase receipts are timely and products meet quality requirements. Using ERP SAP system will utilize control reports to monitor prompt delivery, proper receipt quantities, and on time invoice payments. Will follow policies and guidelines in regards to obtaining required documentation from supplier such as certificates of analysis and certificates of origin.<ul> <li>Convert approved requisitions to purchase orders using ERP SAP system as per policies and procedures. Processing purchases from initiation to receipt. Expediting delivery requirements to insure on-time delivery of materials using system control reports. When required and necessary, prepare and obtain RFQs according to specifications and requirements. Activities may be single or multiple site requirements to ensure inventory levels and operational activities meet customer requirements, inventory targets and sales goals. <li>Maintain Purchasing Info Records and source list for materials with updated pricing for assigned products as directed by the Strategic Buyer. Maintain customer delivery requirements and assist finance / marketing in projecting accurate gross margin while minimizing supply risk. <li>Review vendor invoices regarding quantity and price discrepancies and assist in establishing standard cost. Maintain vendor disbursement within discount periods and assignment of correct purchase price variance account. <li>Issue and follow up on Supplier 'non-conformance" and "root cause" corrective action reports (SCARs). Assist with Supplier scorecards. Insure compliance with RC 14001 and ISO requirements. <li>Process claims for damage/material shortages for appropriate credit memos/replacement receipts. Avoidance of damage goods materials and inventory and/or non-payment of supplier invoices and prompt receipt of replacement goods. <li>Process subcontracting purchase orders according to procedure. Maintain customer delivery requirements and customer service levels. </ul> Minimum Qualifications: <ul> <li>Associates Degree in a science or business area of study or equivalent experience. <li>2 years purchasing or functional experience likely to meet requirements of position. <li>Experience utilizing an integrated ERP computer software package - ideally in SAP. Microsoft Office. <li>Understanding of Supply Chain Concepts. <li>Proven analytical skills and mathematical aptitude with ability to negotiate. <li>Responsibility and decision making experience. <li>Flexibility, proactive attitude, willingness to cause and implement changes.</ul> Preferred Background: <ul> <li>CPM/APIC certification <li>Understanding of distribution and warehouse processes <li>General finance / accounting understanding</ul> Please also visit <a href="http://www.biophaseinc.com" rel="nofollow">http://www.biophaseinc.com</a> to view additional opportunities in San Diego!]]>

<![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a Technical Writer/Sourcing Contract Manager to work for a leading San Diego biotechnology company. Technical Writer/Sourcing Contract Manager This temporary position is to provide technical expertise to facilitate the procurement of chemicals and biological materials. This position is responsible for reviewing production protocols, developing technical transfer packages and providing technical support to 3rd party suppliers. The ideal candidate will possess 5 - 7 years of laboratory experience, preferably in the bioscience, life science, pharmaceutical or chemical industry. This is an Ideal role for an individual with firsthand laboratory experience, who is more interested in the efficient dissemination of scientific information rather than hands-on experimental work. Key Responsibilities: * Interpret/translate, organize and communicate technical/scientific correspondence * Effectively construct, interpret and clearly communicate a variety of instructions furnished in a variety of formats (e.g., written, oral, diagram, or schedule) * Partner with Strategic Sourcing Department to prepare and solicit competitive bids, & evaluate those offerings while developing a reduced & preferred supply base to achieve the lowest total cost of ownership * Support Supplier Management program (supplier qualifications, audits, etc.) * Support New Product Introduction * Develop practical technical solutions to sourcing problems or issues in situations where only limited information is available * Access and utilize database resources and conduct other scientific internet research Minimum Qualifications: * BS in chemistry, biology or other life science or an equivalent combination of education, training and/or experience from which comparable knowledge, skill and abilities have been attained * 1 - 2 years related experience researching, writing, editing and proofing scientific documents * Strong background in biology and organic chemistry * Excellent scientific writing ability * Ability to work independently as well as within a collaborative work environment * Meticulous attention to detail Preferred Qualifications: * Background in biology and organic chemistry * Strong analytical & problem-solving skills * Ability to manage multiple projects simultaneously * Strong proficiency in Microsoft Excel, PowerPoint, and SAP * Illustration skills are desired Please also visit <a href="http://www.biophaseinc.com" rel="nofollow">http://www.biophaseinc.com</a> to view additional opportunities in San Diego!]]>

<![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a Purchasing Supervisor to work for a leading San Diego biotechnology company. Purchasing Supervisor This position is responsible for the day to day supervision of the purchasing team. The primary objective is to lead the team to assure continuity of supply within Supply Chain, develop standardized processes & reports to optimize Buyer performance, incorporate best practices aligned to Corporate Strategic Sourcing, and deliver superior value to the organization. The candidate will be responsible for raw materials/finished goods, equipment, and outsourced operations for the Bioscience Business. This position will interact with Corporate Strategic Sourcing and Business Leadership assisting in the implementation of sourcing projects, category management initiatives, and the standardization of processes across the organization. The ideal candidate will possess 10+ years of purchasing experience with a minimum of 5 years in a supervisory role, preferably in the bioscience, life science, pharmaceutical or chemical industry. Key Responsibilities: * Supervise day to day on-site purchasing activities & purchasing staff * Establish departmental performance goals and execute plans to meet objectives * Lead Operational Purchasing Team and provide guidance to achieve goals while leveraging individual strengths and promoting a team environment * Oversee development, maintenance and control of robust purchasing policies and procedures * Manage monthly purchasing metrics, identify issues and propose resolutions to site management and key stakeholders * Ensure integrity of purchasing master data * Identify, evaluate, and develop new reliable sources for existing or new products or services * Partner with Quality Assurance and HSSE to perform supplier evaluations/audits * Prepare and solicit competitive bids, & evaluate those offerings while developing a reduced & preferred supply base to achieve the lowest total cost of ownership * Work with Legal Department to execute CDA's and Supply Agreements * Manage and administer contracts and purchase orders from award to completion * Manage technical transfer to contract manufacturing suppliers * Work in tandem with Strategic Sourcing to proactively manage vendor relationships, to effect negotiations with potential or current suppliers to obtain maximum value, and measure supplier performance using KPI's and scorecards * Partner with Strategic Sourcing to develop and lead Supplier Management programs that focus on Quality, Productivity and Innovation, develop synergies and alternate sources of supply * Assure sourcing plans and decisions made are congruent with organizational objectives and sourcing strategies. * Collaborate cross-functionally to create operational efficiencies (e.g. Production, Quality Assurance, Planning, Technical Support) * Maintain effective relationships with key internal customers, ie. Marketing, technical, quality, HSSE etc. * Stay abreast of price trends and processes in markets that support the respective business and the Bioscience industry * Provide exceptional customer support with highest ethical standards * Hiring, Performance management of employees * Assist in supplier audits * Assisting in Strategic Sourcing in Supplier relationship management Minimum Qualifications: * Four-year degree in Supply Chain Management, Engineering or Science field. * 10+ years purchasing experience. * Minimum of 7 years experience in leading and developing a team of procurement or operations professionals. * Proven history of effectively managing teams and implementing organizational change. * Able to multi-task in an energy-charged, fast-paced environment. * Demonstrated experience in contracts, negotiating, procurement, risk assessment, Six Sigma and Lean Management. * Excellent Interpersonal, communication and negotiation skills. * ERP purchasing/order management experience, Conversant in MS Word, Excel, and PowerPoint. Preferred Background: * SAP knowledge & experience * Knowledge of ISO, GMP requirements * 7-10 years experience in the bioscience, life science, pharmaceutical or chemical industry * Strong analytical & problem-solving skills * Ability to manage multiple projects simultaneously * Professional Certifications (e.g. CPSM) * Experience in Six Sigma, Lean Manufacturing or other process improvements is a plus Please also visit <a href="http://www.biophaseinc.com" rel="nofollow">http://www.biophaseinc.com</a> to view additional opportunities in Southern California!]]>

<![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a Microbiology Supervisor to work for a leading San Diego biotechnology company. Microbiology Supervisor SUMMARY Responsible to ensure compliance to domestic and international standards with regards to the monitoring of environmental systems (i.e. HVAC/cleanroom, Compressed Air, Water), sterilization of medical devices, biocompatibility testing of materials, supervision and training of laboratory technicians. ESSENTIAL DUTIES AND RESPONSIBILITIES * Supervise daily operation and testing requirements for the environmental monitoring program. * Establish and perform the environmental monitoring program for the Heating Ventilation & Air Conditioning (HVAC), Compressed Air and Pharmaceutical Grade Water Systems. * Supports process improvements by designing equipment, process and test method validations. * Establish and perform environmental monitoring program tracking and trending data base, data entry and quarterly reporting. * Establish and perform environmental monitoring excursion communication, reporting, investigation, disposition and corrective action process. Requires multi-department communication and approval for coordination of work performed (i.e. Operations, QC, Sanitization, Facilities and QA). * Assure compliance of the sterilization program for sterile implantable devices by performing scheduled re-qualification, supplier audits, new product qualifications, challenge and bioburden testing when necessary. REQUIREMENTS * Bachelor's degree (B.S.) from a four-year college or university; Microbiology or related field. * 3+ years of related experience. * Must have knowledge of the following 21 CFR 820, ISO 13485, CMDR, and EEC93/42, U.S. and E.U. Pharmacopeia, International Organization for Standardization (ISO) 10993, 14644, ISO 14971 and other Risk guidance standards to create the processes and supporting documentation. * Additional Areas of possible competence: o Gamma, E-beam and ETO Sterilization, Biocompatibility of Materials, Cleanroom Microbiology o Solid understanding of international and domestic medical device GMPs/Quality System Requirements o Solid understanding of international and domestic environmental monitoring requirements. o Develop and perform test method validations in support of microbiology operations (e.g. Endotoxin Testing) and interpret the results. Please also visit <a href="http://www.biophaseinc.com" rel="nofollow">http://www.biophaseinc.com</a> to view additional opportunities in San Diego County!]]>

<![CDATA[About Ambrx: Ambrx, Inc. is a biopharmaceutical company with a mission to deliver breakthrough protein therapeutics. Ambrx is based on a fundamental advance in protein biosynthesis that enables the company to genetically engineer proteins with new amino acid building blocks beyond the common twenty, enabling the biosynthesis of proteins with new physical, chemical and pharmacological properties. At Ambrx, we are dedicated to assembling and developing an exceptional team and a breakthrough technology to create the next generation of protein-based medicines. Description: Ambrx is seeking an independent and highly motivated Research Associate to be a key member of a dynamic Biotech organization. The successful candidate will possess the following qualifications: Requirements: - B.S. or Master Degree in Biochemical Engineering, Chemical Engineering, Biochemistry or related field with 1+ years of relevant laboratory experience. - Both hands-on experience and scientific knowledge in protein purification process development using column chromatography and filtration techniques are required. - Familiarity with programming and operating AKTA™ FPLC, TFF systems as well as basic analytical techniques for protein quantitation and characterization using gel electrophoresis, HPLC, and protein assays are also required. - Previous experience in purification process development, protein production at various scales including endotoxin-free material for animal studies are highly desired. - Excellent communication, organization and collaborative skills are essential. - Attention to detail and ability to generate accurate and reproducible results a must - The ability to multi-task and work effectively in a fast-paced environment with minimal supervision is critical To be considered as an applicant, please submit your resume/CV referencing the specific position of interest and position code to careers@ambrx.com. Applicants whose qualifications and experience most closely match the requirements of the position will be reviewed. Candidates will only be contacted for evaluative discussions. Ambrx offers competitive compensation & benefits. EOE]]>

<![CDATA[IMPORTANT NOTE: WE ARE LOOKING FOR A SPECIFIC SKILLSET. We cannot accept candidates who do not meet ALL of our qualifications. -EXPERIENCED ONLY! Your resume will NOT be considered unless you have actual experience performing asbestos microscopy. -PLEASE DO NOT APPLY UNLESS YOU HAVE ACTUAL EXPERIENCE PERFORMING ASBESTOS MICROSCOPY -Only applicants who live in the U.S. and are authorized to work in the U.S. will be considered. -candidate will have to undergo company training in our San Bruno, California laboratory for approximately 2-3 weeks (all expenses will be paid). -we are open to providing relocation assistance depending on the candidate. WHO WE ARE LOOKING FOR…… EMLab P&K (a division of TestAmerica), the leading commercial indoor air quality testing laboratory in North America, is seeking a motivated scientist for our San Diego, California laboratory with experience in asbestos microscopy. This laboratory is one of our remote labs and is staffed with three (3) microscopists (including this position) in addition to other supporting staff. Your core responsibilities will include the analysis of bulk and air samples using PLM and PCM for asbestos. Experience with TEM would be desirable. Candidates who apply should be knowledgeable, thorough and efficient and be able to meet our high standards for quality. Qualifications: * BA/BS or Masters in Biology, Microbiology, Geology or related field * MINIMUM 1-2 years of experience performing asbestos microscopy REQUIRED * Candidates with mycological analysis experience in addition to Asbestos microscopy experience are an added-plus Candidates will not be considered unless they meet the minimum requirements as listed above. ABOUT US...... EMLab P&K (a division of TestAmerica) is recognized as one of the leading commercial indoor air quality laboratories in North America specializing in the analysis of air and surface samples for asbestos, bacteria, legionella, and fungi. Our goal is to provide the highest quality analysis and service in the industry. Clients include industrial hygienists, laboratories, hospitals, public health departments, professional service firms and other IAQ professionals. EMLab P&K has helped pioneer today’s IAQ industry with MoldRange™ , MoldScore™ and over 100 publications and abstracts. We offer a full line of IAQ and IH equipment and supplies; and we provide LabServe™, a 24-hour, online customer service, which controls data management, custom report formatting, access to secure archives of projects and reports. Additionally, we have 12 locations across the country; and nearly all are accredited by programs that include AIHA EMLAP, NVLAP, and additional state certifications and licenses. EMLab P&K ( a division of TestAmerica, Inc.) provides a comfortable work environment and a comprehensive, highly competitive compensation and benefits package – at low cost to the employee - including medical, dental, vision, (we also offer optional items at competitive rates and at an additional cost(s)that include: auto/home/renter insurance, pet insurance, legal insurance, and a competitive discount from a well-known wireless company for your cell phone and wireless needs). A 401(k) plan is also offered. In addition, life insurance coverage at 2x your annual salary is provided at no cost to the employee. Additional life insurance coverage (over-and-above what the company provides) is available at excellent rates, and, life insurance for your spouse and/or dependents – up to a designated maximum amount - is also available at a nominal cost If you would like to know more about us, please visit our website at www.emlabpk.com ]]>

<![CDATA[IMPORTANT NOTE: WE ARE LOOKING FOR A SPECIFIC SKILLSET. We cannot accept candidates who do not meet ALL of our qualifications. WHO WE ARE LOOKING FOR….. EMLab P&K, the leading commercial indoor air quality testing laboratory in North America, is seeking a motivated scientist in the San Diego, California area with experience in the biological sciences. This laboratory is one of our remote labs and is staffed with three (3) microscopists (including this position) in addition to other supporting staff. Your core responsibilities will include the analysis of non-culturable surface and air samples for fungi. Candidates who apply should be career oriented, willing to learn, thorough, efficient, and be able to meet our high standards for quality. Qualifications: * BA/BS or Masters in Plant Biology, Biology, Microbiology, or any other life science with a minimum of eight (8) semester hours of microbiology. * Must have three (3) years of laboratory experience with two (2) of those years involving both spore trap and direct exam experience. * Candidates with asbestos analysis experience in addition to mycological microscopy experience are an added-plus IMPORTANT NOTES: 1. we are open to providing relocation assistance depending on the candidate 2. candidate will have to undergo company training in our San Bruno, California laboratory for approximately 2-3 weeks (all expenses will be paid). 3. At this time we are ONLY accepting applicants who have authorization to work in the United States and who currently live in the United States. ABOUT US...... EMLab P&K (a division of TestAmerica) is recognized as one of the leading commercial indoor air quality laboratories in North America specializing in the analysis of air and surface samples for asbestos, bacteria, legionella, and fungi. Our goal is to provide the highest quality analysis and service in the industry. Clients include industrial hygienists, laboratories, hospitals, public health departments, professional service firms and other IAQ professionals. EMLab P&K has helped pioneer today’s IAQ industry with MoldRange™ , MoldScore™ and over 100 publications and abstracts. We offer a full line of IAQ and IH equipment and supplies; and we provide LabServe™, a 24-hour, online customer service, which controls data management, custom report formatting, access to secure archives of projects and reports. Additionally, we have 12 locations across the country; and nearly all are accredited by programs that include AIHA EMLAP, NVLAP, and additional state certifications and licenses. EMLab P&K ( a division of TestAmerica, Inc.) provides a comfortable work environment and a comprehensive, highly competitive compensation and benefits package – at low cost to the employee - including medical, dental, vision, (we also offer optional items at competitive rates and at an additional cost(s)that include: auto/home/renter insurance, pet insurance, legal insurance, and a competitive discount from a well-known wireless company for your cell phone and wireless needs). A 401(k) plan is also offered. In addition, life insurance coverage at 2x your annual salary is provided at no cost to the employee. Additional life insurance coverage (over-and-above what the company provides) is available at excellent rates, and, life insurance for your spouse and/or dependents – up to a designated maximum amount - is also available at a nominal cost If you would like to know more about us, please visit our website at www.emlabpk.com ]]>

<![CDATA[The qualified Technician will be part of a team responsible for the transfer of both existing and new assays from R&D to Laboratory Operations. The selected candidate will be responsible for implementing production procedures to optimize manufacturing processes and regulatory requirements. In this role, you will: * Assist Process Development in developing scalable processes with higher product yield and reduced manufacturing costs. * Write Standard Operating Procedures (SOPs) and other laboratory documents * Act as a liaison between the research and development teams to ensure the process designs are compatible * Assist with maintenance of production equipment The Technician will possess the following qualifications: * BS with 2+ years of experience * Manufacturing experience in a GMP setting required * Diagnostic product experience preferred * High complexity CLIA/CAP experience preferred ]]>

<![CDATA[Title: Research and Clinical Project Director Reports to: CEO & Chief Scientific Officer Description Summary: Reporting to the CEO and Chief Scientific Officer, the Research and Clinical Project Director will manage multiple research and clinical programs of medical device treatments against infectious disease and cancer-related illnesses. This position requires a strong understanding of medical project management processes and the ability to effectively communicate with industry partners and collaborators. Duties and Responsibilities: • Actively develop, track and report on program plan, detailed project schedule, research and clinical study status, and program deliverables. • Assist in the development and administration of research and clinical studies both internally and with industry partners and collaborators. Requirements: • Five to seven years equivalent experience in Infectious Disease and Molecular Biology and/or Cancer fields • Demonstrated experience in monitoring and managing new and ongoing clinical trials and/or research projects • Ability to effectively interact with all members of research and clinical trial teams • Ability to work independently in a small company environment is essential Competitive salary commensurate with experience ]]>

<![CDATA[ Associate Scientist Located in beautiful San Diego, our company is a growing, state of the art clinical testing laboratory providing drug testing services for physicians nationwide. We offer a competitive salary and benefits, a positive work environment and the opportunity to work with a highly motivated and talented staff. Job Description; This is a full time position in a fast-paced clinical toxicology laboratory using state of the art LC/MS/MS technology for the detection of prescription and illicit drugs. In addition to maintaining and perfecting all LC/MS/MS instruments and processes, this person will be involved in research and development of new tests and techniques at the forefront of mass spectrometry. As a key member of our scientific team you will also be responsible for maintaining the operation of the lab and reviewing quality control and chromatographic data before its release to physicians. We encourage and support publishing as well as public presentations to select audiences nationally and internationally. Education: BS degree and 4-6 years of experience, or Ph.D. and 0-2 years of experience. The candidate must have extensive hands on experience using mass spectrometry and HPLC. No phone calls, please. ]]>

<![CDATA[Leading Mira Mesa biotech seeks a Technical Writer/Sourcing Contract Manager.position is to provide technical expertise to facilitate the procurement of chemicals and biological materials. This position is responsible for reviewing production protocols, developing technical transfer packages and providing technical support to 3rd party suppliers for the Bioscience Business at the San Diego, CA location. The ideal candidate will possess 5 - 7 years of laboratory experience, preferably in the bioscience, life science, pharmaceutical or chemical industry. This is an Ideal role for an individual with firsthand laboratory experience, who is more interested in the efficient dissemination of scientific information rather than hands-on experimental work. Key Responsibilities: • Interpret/translate, organize and communicate technical/scientific correspondence • Effectively construct, interpret and clearly communicate a variety of instructions furnished in a variety of formats ( e.g., written, oral, diagram, or schedule) • Partner with Strategic Sourcing Department to prepare and solicit competitive bids, & evaluate those offerings while developing a reduced & preferred supply base to achieve the lowest total cost of ownership • Support Supplier Management program (supplier qualifications, audits, etc.) • Support New Product Introduction • Develop practical technical solutions to sourcing problems or issues in situations where only limited information is available • Access and utilize database resources and conduct other scientific internet research Minimum Qualifications: • BS in chemistry, biology or other life science or an equivalent combination of education, training and/or experience from which comparable knowledge, skill and abilities have been attained • 1 - 2 years related experience researching, writing, editing and proofing scientific documents • Strong background in biology and organic chemistry • Excellent scientific writing ability • Ability to work independently as well as within a collaborative work environment • Meticulous attention to detail Preferred Qualifications: • Background in biology and organic chemistry • Strong analytical & problem-solving skills • Ability to manage multiple projects simultaneously • Strong proficiency in Microsoft Excel, PowerPoint, and SAP • Illustration skills are desired Please note, this is a 1 year contract position. ]]>

<![CDATA[Qualigen, Inc. (qualigeninc.com) develops, manufactures, and distributes the patented FastPack System which is the first blood testing system custom designed to perform quantitative immunoassay tests in the physician’s office laboratory. The FastPack System includes tests for prostate cancer, thyroid disorders, pregnancy, and male aging disorders. Several exciting new diagnostic assays are currently in development. Come join our team of talented professionals! We are looking for a temporary Manufacturing Technician (this is a temp to hire position). Position Reports To: Packaging Supervisor Position Summary: Responsible for the production of kit components by filling bulk reagents using automated filling equipment along with assembly of final diagnostic test kits according to written manufacturing instructions. Responsibilities: •Responsible for all aspects related to reagent filling and Packaging. o Operation and maintenance of filling equipment. o In process testing o Data entry into Excel spread sheets o Perform accurate counts of final product produced and reagent used. o Label imprinting. o Labeling and packaging of final product. o Document review. o Maintain equipment and packaging area in a clean and functional state. o Inventory control and transaction (ERP). Preferred Skills: Education: High School diploma. Experience: 1-3 years experience in a packaging and/or manufacturing environment. •Good laboratory skills including laboratory safety, equipment operation and maintenance. •General knowledge of FDA regulations and GMP compliance is a plus. •Good general math and documentation skills. •Experience following written instruction (SOPs). •Good verbal and written communication skills. •Computer knowledge (i.e. Word, Excel and Outlook). EOE]]>

<![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a Technician II/III to work for a leading San Diego biotechnology company. Technician II/III Job Responsibilities The position is responsible for learning and performing all of the manufacturing processes in the Tissue Culture department with close departmental supervision. It will include LN2 tank handling, tissue culture, media preparation, and related assays by learning and following batches records, databases and documentation systems for data input with various departmental databases such as SOP, working instructions, Filemaker Pro and business systems (SAP). Expected to actively participate in continuous improvement process during the working process. Job Requirements * Minimum requirements for this position include a High School Diploma and 3+ years experience or BS degree with minimum of 6 months experience in a manufacturing lab environment is required. * Requires hands-on laboratory experience, performing experiments using lab equipment. * Requires good documentation (maintaining clear and concise records) and effective communication (written and verbal) skills. * The ability to navigate databases and be computer literate is also required. * Requires experience in the handling of sterile products in a sterile environment preferred. * Previous hands-on experience on handling the liquid nitrogen will be a plus. * Must be able to work in a team to meet the in-process testing requirements. * Requires good organization skills and attention to detail. * Requires strong math skills, including knowledge of the metric system unit of measure. * Requires experience with product dilutions and use of a spectrophotometer highly desirable. * Requires basic computer skills, Word and Excel. Requires self-motivated, ability to work with minimum supervision. * Requires proficient learner with new tasks and methods. * Requires good attendance and solid work ethic. Please also visit www.biophaseinc.com to view additional opportunities in San Diego County!]]>

<![CDATA[Our History of Expertise & Quality Focus eBioscience (www.ebioscience.com) scientists have extensive expertise in antibody development, as well as personal histories of raising industry standards for antibody quality. Researchers worldwide have always been assured that their research funding and time are well-invested in eBioscience antibodies. Time and time again, eBioscience reagents have provided Researchers with the consistent, quality data that they expect. eBioscience reagents are utilized by leading laboratories worldwide. Since the company's inception in San Diego in 1999, our products have been widely cited in prestigious journals, including: • Blood • Immunity • Journal of Biological Chemistry • Journal of Experimental Medicine • Journal of Leukocyte Biology • Journal of Immunology • Journal of Virology • Nature • Nature Cell Biology • Nature Immunology • Nature Medicine • Proc. of National Academy of Science • Science Principle Accountabilities Quality Assurance Specialist We are seeking a highly motivated Quality Assurance Specialist who will be responsible for performing various activities pertaining to assuring compliance with applicable regulatory requirements. These activities may include Validation, Customer Complaints, Review of records related to product manufacture, Audits, and QA documentation. Essential Duties and Responsibilities include the following (other duties may be assigned.): • Assist in maintaining systems to ensure company compliance with all applicable regulatory requirements. • Assist in maintaining systems to ensure that all products meet the required specifications. • Assist in the updating and maintenance of documentation to ensure company compliance with all applicable regulatory requirements • Assist in delegating the product testing for complaints. • Perform the completion and timely closure of Customer Complaints. • Perform regular audits of company departments and vendors to ensure compliance to regulations. • Assist in the review and creation of ISO/QSR documentation • Assist in the performance of GMP training. • Help maintain company compliance with Non-Conformance and Corrective/Preventive Action procedures. • Perform Batch Record review • Provide training, as needed • Assist with ISO projects • Special projects as assigned Qualifications: Bachelor’s Degree in a Biological Science, Chemistry, related field or equivalent laboratory experience; minimum of 4 years of experience in in vitro diagnostic, medical device, pharmaceutical or related industry. Highly motivated and dedicated individual with the ability to show initiative and to perform in a multi-task environment; well organized, detail oriented, strong interpersonal and verbal/written communication skills; Ability to work with personnel of all levels; knowledge of QSR,ISO and technical writing capability. Logical thought process with ability to apply ideas to new situations. Strong understanding of basic mathematics with exposure to statistical techniques. Strong working knowledge of Microsoft Office (Word, Excel, PowerPoint and Access). Physical Demands and Work Environment: The physical demands and work environment described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to sit, stand, walk, talk and hear; use hands to finger, handle or feel; and reach with hands and arms. The noise level in the environment is usually moderate. Benefits: We offer an exciting, entrepreneurial environment and a competitive compensation package, including salary, plus performance bonus and benefits (medical/dental and 401k). Plus, we work to maintain the best possible environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where each person feels encouraged to contribute to our processes, decisions, planning and culture. Our company culture is creative, fast-paced and entrepreneurial. We are a right sized environment where you can stand out and make a difference. EOE ]]>

<![CDATA[ What We Do Eppendorf Manufacturing is a state-of-the-art production facility for pipette tips and related accessories that is located in Enfield, Connecticut, convenient to the major airports in Boston and New York. We are the sole US manufacturing subsidiary of Eppendorf AG, a world leader in laboratory instruments and consumables for biotechnology research, headquartered in Hamburg, Germany. Our 24-hour operation incorporates the latest technology and best materials to produce safe, precise and reliable tips for life science and clinical research. Injection molding takes place in clean-room conditions that have obtained ISO certification. Eppendorf companies in the United States include Eppendorf, Inc. (regional administration), Eppendorf North America (sales, marketing and field service) and Brinkmann-Eppendorf Services, Inc. (in-house service and repair). As part of a global company and growing entity you will be part of a progressive and high-energy team, focused on bringing quality products to market and excelling in quality customer service. Instrument Service Technician – Calibration & Instruments, San Diego, CA Job Description <ul><li> Diagnoses and repairs Eppendorf electronic instrumentation and all brands of pipettes within the designated Service Repair Center. May be required to perform these duties and responsibilities within the field in rare circumstances as determined by the supervisor </li><li> Executes the determined service product- Follows any established repair or customer protocols, tests instruments to ensure conformance to factory specifications. Determines and completes necessary cleaning, replacement, adjustment or repair. Records calibration test measurements in and administers test certificates as required. </li><li> Achieve high levels of customer satisfaction. Must be an effective communicator from managing expectations through follow-up in a positive, customer centric, error free and professional manner. Primary contacts will be internal business partners with occasional external customer contact. </li><li> Establish and maintain a high degree of technical knowledge pertaining to the repair, maintenance, and quality system requirements of Eppendorf equipment and services. Satisfactory completion of Eppendorf initial and ongoing service training. </li><li> Responsible for receiving, shipping and coordinating the receipt and return of customer’s property in and out of the Service Repair Center. </li><li> Administrative Excellence. Responsible to ensure service is completed accurately and all system needs are addressed in a timely manner with the proper detail to ensure invoicing and quality management system requirements. </li><li> Supports the Sales organization where requested and the sales of service products and liquid handling promotion programs. </li><li> Enforces, cooperates with and complies with all of the company’s policies, procedures, rules and regulations. Exercises all safety precautions as required and responsible for proper care of company equipment. </li></ul> Skills, Education and Certification <ul><li> Associate's degree (A.A.) or equivalent from a two-year college or technical school; or equivalent military training, and three to five years’ related experience and/or training. </li><li> Valid driver's license required. Must maintain a good driving record. </li></ul> To apply for this position, please visit eppendorfna.com and click on "Corporate" then click "Jobs and Careers" then goto "Job Offers" Why Work for Us? You will be working in a professional environment. In return for your contributions, you will receive a competitive salary and an excellent company paid benefits package. A sampling of our company paid benefits include: <ul><li> comprehensive medical </li><li> comprehensive dental </li><li> basic life insurance </li><li> short and long term disability </li><li> tuition reimbursement program </li><li> paid vacation </li><li> paid holidays </li><li> paid sick and personal days </li><li> 401k plan </li><li> plus more! </li></ul> Eppendorf Manufacturing Corporation is an equal opportunity employer. M/F/V/H ]]>

<![CDATA[San Diego biotech company is seeking a part-time Associate Scientist. This is an entry level position with potential for full time. The ideal candidate should be motivated, detail-oriented, organized and disciplined with good record keeping. Good interpersonal and teamwork skills are essential. The position is for the evening shift. Pipetting skills are required and at least 1 year of previous lab experience preferred. Must be flexible in schedule. Please submit your resume with 2 references for consideration. We regretfully are unable to respond individually to each person interested in our company, or answer inquiries regarding the status of a particular resume. If there is interest in interviewing you for an available position within our company, a representative from the Human Resources Department will contact you in the near future.]]>

<![CDATA[As a member of the Protein Science department the successful candidate will work within a dynamic team environment to develop and implement broad project plans and perform experiments for the production, purification and analysis of protein and protein conjugates. Responsibilities will include planning projects, generating and analyzing data, participating to multifunctional project teams and managing the work of junior staff members. The successful candidate will be expected to perform the following activities under minimal supervision: - Participate in the evaluation of new developments in the field of protein production and purification and reduce them to practice in the laboratory. - Participate to multifunctional project teams as a department representative in order to advance CovX’ pipeline. - Develop production processes and analytical approaches to support the development of CovX’s protein conjugation platforms. Qualifications: - Ph.D. with 7-10 years of biotech experience in a field connected to Protein Science (e.g. Protein Engineering, Protein formulation, Biological Process Development, etc…). - Experience with molecular Biology (knowledge of expression systems a plus). - Protein handling techniques (chromatography and TFF experience a plus). - Proven capacity to follow complex projects through completion. - Ability to effectively participate in multidisciplinary project teams. - Strong troubleshooting skills and innovative thinking to solve scientific problems. Please submit resumes for Req. #938714 to www.pfizer.com Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must have authorization to work for Pfizer in the U.S. In certain circumstances it may be advantageous to Pfizer to support the application(s) for temporary visa classification and/or sponsor applications for permanent residence so that a foreign national colleague can accept or remain in a work assignment in the U. S. For certain classes of temporary visas, the resulting work authorization may be specific to Pfizer and the specific job and/or work site. Pfizer may at its business discretion decide to or refrain from obtaining, maintaining and/or extending the temporary visa status and/or sponsoring a colleague for permanent residency and /or employment eligibility, considering factors such as availability of qualified U.S. workers and the colleague's long-term prospects for securing lawful permanent residence, among other reasons. Employment applicants requiring immigration sponsorship must disclose, when initial application for employment is made, whether or not they are legally authorized to work for Pfizer in the U.S. and, if so, whether that authorization permits them to work in the job they seek. In no case should Pfizer's support of a colleague's temporary visa application or sponsorship of a colleague for permanent residence be construed to guarantee success of that application or amend or otherwise invalidate the "at-will" employment relationship between the colleague and Pfizer. Throughout our 153 years, a legacy of caring for others has been at the heart of everything we do at Pfizer. This commitment is no less important when it comes to our employees. Pfizer wants to ensure that employees have resources to help them develop and succeed both in their careers and personal lives. One way we can achieve this is through our comprehensive benefits program, which offers employees and their eligible dependents the variety and flexibility to help address their needs at different stages in life. CovX offers exciting careers for passionate, creative people who thrive on challenge and are motivated by the opportunity to have a big impact. Located in San Diego, California, CovX is a part of Pfizer’s BioTherapeutics R&D Business Unit. Since its founding, CovX has made advances toward building a portfolio of product candidates. We use our proprietary technology to rapidly discover and develop long-acting biological therapeutics. The CovX technology unites the therapeutic attractiveness of peptides with the beneficial properties of antibodies, resulting in a new biopharmaceutical called a CovX-Body. The highly flexible nature of our technology enables us to identify high-value biological targets, efficiently create CovX-Bodies, and expeditiously move candidates to pre-clinical development and clinical evaluation. To apply for this position, please <a href="http://posttrak.arbita.net/cgi-bin/PostTrak.cgi?RefCode=R4489276008250" rel="nofollow">CLICK HERE</a> ARBPFZ4070-741150]]>

<![CDATA[As a member of the Protein Science department the candidate will work within a dynamic team environment to develop techniques for the production, purification and analysis of CovX-body molecules. Responsibilities will include generating, analyzing and presenting data, drafting development reports and support discovery and pre-clinical/clinical activities. The successful candidate will be expected to perform the following activities under the direction of senior team members: - Participate in the evaluation of new developments in the field of protein purification. - Develop and routinely run FPLC, HPLC and other relevant methods to characterize and purify various recombinant proteins. - Perform subcloning and protein expression. - Perform in-process assays (spectrophotometry, SDS-PAGE, SEC-HPLC, activity assays). - Generate method development and study reports. - Maintain and calibrate equipment. Qualifications: - BS degree in Chemistry/Biochemistry or related field plus 0-4 years relevant industry experience. - Experience with protein handling techniques (chromatography and filtration experience a plus). - High level of initiative, capacity to plan scientific experiment creatively. - Demonstrated attention to detail. - Ability to effectively participate in multidisciplinary project teams. Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must have authorization to work for Pfizer in the U.S. In certain circumstances it may be advantageous to Pfizer to support the application(s) for temporary visa classification and/or sponsor applications for permanent residence so that a foreign national colleague can accept or remain in a work assignment in the U. S. For certain classes of temporary visas, the resulting work authorization may be specific to Pfizer and the specific job and/or work site. Pfizer may at its business discretion decide to or refrain from obtaining, maintaining and/or extending the temporary visa status and/or sponsoring a colleague for permanent residency and /or employment eligibility, considering factors such as availability of qualified U.S. workers and the colleague's long-term prospects for securing lawful permanent residence, among other reasons. Employment applicants requiring immigration sponsorship must disclose, when initial application for employment is made, whether or not they are legally authorized to work for Pfizer in the U.S. and, if so, whether that authorization permits them to work in the job they seek. In no case should Pfizer's support of a colleague's temporary visa application or sponsorship of a colleague for permanent residence be construed to guarantee success of that application or amend or otherwise invalidate the "at-will" employment relationship between the colleague and Pfizer. Please submit resumes for Req. #938505 to www.pfizer.com Throughout our 153 years, a legacy of caring for others has been at the heart of everything we do at Pfizer. This commitment is no less important when it comes to our employees. Pfizer wants to ensure that employees have resources to help them develop and succeed both in their careers and personal lives. One way we can achieve this is through our comprehensive benefits program, which offers employees and their eligible dependents the variety and flexibility to help address their needs at different stages in life. CovX offers exciting careers for passionate, creative people who thrive on challenge and are motivated by the opportunity to have a big impact. Located in San Diego, California, CovX is a part of Pfizer’s BioTherapeutics R&D Business Unit. Since its founding, CovX has made advances toward building a portfolio of product candidates. We use our proprietary technology to rapidly discover and develop long-acting biological therapeutics. The CovX technology unites the therapeutic attractiveness of peptides with the beneficial properties of antibodies, resulting in a new biopharmaceutical called a CovX-Body. The highly flexible nature of our technology enables us to identify high-value biological targets, efficiently create CovX-Bodies, and expeditiously move candidates to pre-clinical development and clinical evaluation. To apply for this position, please <a href="http://posttrak.arbita.net/cgi-bin/PostTrak.cgi?RefCode=R2777276008248" rel="nofollow">CLICK HERE</a> ARBPFZ4064-739646]]>

<![CDATA[As a Sr. Research Associate in the Biology Department, this position will contribute to the CovX portfolio by utilizing in vitro molecular models as well as in vivo disease models for drug discovery. Specific responsibilities to include: - Execute cell-based functional assays to validate targets and screen potential new biological entities, particularly in the area of metabolic disease. - Support creation of novel in vitro test systems using genetic approaches such as cloning and reporter gene construction. - Utilize in vivo disease models to triage compounds and verify mechanism of action ex vivo. - Engage in projects, generate and evaluate project ideas, work collaboratively with other groups to achieve objectives and timelines. - Provide effective and detail-focused communication and documentation of research results. Qualifications: Applicant should have a PhD and 0-3 years industry experience or an MS and 5-10 years industry experience. The applicant should have experience in cell-based assay development and execution, as well as in vivo disease models, and a track record of using these techniques in metabolic disease therapeutic drug discovery, particularly as applied to biotherapeutics. Expertise in immunohistochemistry is highly desired, as is experience with gene expression analysis. The successful candidate is expected to design and execute experiments independently, and communicate data and ideas to other team members within Biology and to the company. Excellent oral and written communications skills are a must, and proficiency with standard office computer software in required. Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must have authorization to work for Pfizer in the U.S. In certain circumstances it may be advantageous to Pfizer to support the application(s) for temporary visa classification and/or sponsor applications for permanent residence so that a foreign national colleague can accept or remain in a work assignment in the U. S. For certain classes of temporary visas, the resulting work authorization may be specific to Pfizer and the specific job and/or work site. Pfizer may at its business discretion decide to or refrain from obtaining, maintaining and/or extending the temporary visa status and/or sponsoring a colleague for permanent residency and /or employment eligibility, considering factors such as availability of qualified U.S. workers and the colleague's long-term prospects for securing lawful permanent residence, among other reasons. Employment applicants requiring immigration sponsorship must disclose, when initial application for employment is made, whether or not they are legally authorized to work for Pfizer in the U.S. and, if so, whether that authorization permits them to work in the job they seek. In no case should Pfizer's support of a colleague's temporary visa application or sponsorship of a colleague for permanent residence be construed to guarantee success of that application or amend or otherwise invalidate the "at-will" employment relationship between the colleague and Pfizer. Please submit resumes for Req. #938512 to www.pfizer.com Throughout our 153 years, a legacy of caring for others has been at the heart of everything we do at Pfizer. This commitment is no less important when it comes to our employees. Pfizer wants to ensure that employees have resources to help them develop and succeed both in their careers and personal lives. One way we can achieve this is through our comprehensive benefits program, which offers employees and their eligible dependents the variety and flexibility to help address their needs at different stages in life. CovX offers exciting careers for passionate, creative people who thrive on challenge and are motivated by the opportunity to have a big impact. Located in San Diego, California, CovX is a part of Pfizer’s BioTherapeutics R&D Business Unit. Since its founding, CovX has made advances toward building a portfolio of product candidates. We use our proprietary technology to rapidly discover and develop long-acting biological therapeutics. The CovX technology unites the therapeutic attractiveness of peptides with the beneficial properties of antibodies, resulting in a new biopharmaceutical called a CovX-Body. The highly flexible nature of our technology enables us to identify high-value biological targets, efficiently create CovX-Bodies, and expeditiously move candidates to pre-clinical development and clinical evaluation. To apply for this position, please <a href="http://posttrak.arbita.net/cgi-bin/PostTrak.cgi?RefCode=R2773276008244" rel="nofollow">CLICK HERE</a> ARBPFZ4064-739641]]>

<![CDATA[As a key member of the Biology Department, this position will contribute to the CovX portfolio by coordinating the workflow between the vivarium and the drug discovery teams. Specific responsibilities to include: - Managing the ordering, stocking, and day-to-day workflow of vivarium - Collecting and recording data from in vivo pharmacology models - Animal husbandry responsibilities up to 20 hrs/wk - Engage in projects and work collaboratively with other groups to achieve objectives and timelines - Effective and detail-focused communication and documentation of research results Qualifications: Successful applicant will have a BS with 1-3 years experience in a relevant biological science, or an M.S. with 0-2 years industry experience. The qualified individual must be a team player with excellent verbal and written communication skills. Excellent in vivo skills, particularly as applied to biotherapeutic drug discovery, is required. Experience with tissue processing and/or immunohistochemistry, and knowledge of IACUC compliance procedures, are advantageous. Please submit resumes for Requisition #938779 to www.pfizer.com Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must have authorization to work for Pfizer in the U.S. In certain circumstances it may be advantageous to Pfizer to support the application(s) for temporary visa classification and/or sponsor applications for permanent residence so that a foreign national colleague can accept or remain in a work assignment in the U. S. For certain classes of temporary visas, the resulting work authorization may be specific to Pfizer and the specific job and/or work site. Pfizer may at its business discretion decide to or refrain from obtaining, maintaining and/or extending the temporary visa status and/or sponsoring a colleague for permanent residency and /or employment eligibility, considering factors such as availability of qualified U.S. workers and the colleague's long-term prospects for securing lawful permanent residence, among other reasons. Employment applicants requiring immigration sponsorship must disclose, when initial application for employment is made, whether or not they are legally authorized to work for Pfizer in the U.S. and, if so, whether that authorization permits them to work in the job they seek. In no case should Pfizer's support of a colleague's temporary visa application or sponsorship of a colleague for permanent residence be construed to guarantee success of that application or amend or otherwise invalidate the "at-will" employment relationship between the colleague and Pfizer. Throughout our 153 years, a legacy of caring for others has been at the heart of everything we do at Pfizer. This commitment is no less important when it comes to our employees. Pfizer wants to ensure that employees have resources to help them develop and succeed both in their careers and personal lives. One way we can achieve this is through our comprehensive benefits program, which offers employees and their eligible dependents the variety and flexibility to help address their needs at different stages in life. CovX offers exciting careers for passionate, creative people who thrive on challenge and are motivated by the opportunity to have a big impact. Located in San Diego, California, CovX is a part of Pfizer’s BioTherapeutics R&D Business Unit. Since its founding, CovX has made advances toward building a portfolio of product candidates. We use our proprietary technology to rapidly discover and develop long-acting biological therapeutics. The CovX technology unites the therapeutic attractiveness of peptides with the beneficial properties of antibodies, resulting in a new biopharmaceutical called a CovX-Body. The highly flexible nature of our technology enables us to identify high-value biological targets, efficiently create CovX-Bodies, and expeditiously move candidates to pre-clinical development and clinical evaluation. To apply for this position, please <a href="http://posttrak.arbita.net/cgi-bin/PostTrak.cgi?RefCode=R5511276008237" rel="nofollow">CLICK HERE</a> ARBPFZ4074-742069]]>

<![CDATA[Sapphire Energy is a venture capital backed company developing next generation biofuels based on recent advances in metabolic engineering. The company’s focus is the commercialization of high performance, low cost, and low carbon footprint biofuels that are direct replacements for conventional gasoline, diesel, and jet fuel. We seek a motivated algae physiologist to join the Strain Evaluation team. Responsibilities: •Evaluation and quality control of strains generated in the lab. The daily duties will involve characterization of new strains including growth at different media and environmental conditions – in various growth systems and reactors •Growth and maintenance of fresh cultures for experiments and on plates •Analyze data, prepare scientific reports and present to co-workers •Other standard microbiological activities •This position requires fulfilling certain weekend duties Qualifications: •Prior knowledge and experience with microbiology and sterile work is required •Prior knowledge and experience in algal physiology and microscopy is preferred •Detail oriented and very •Organization a must •Comfortable with calculations and charting using Microsoft Excel •Able to remain focused under pressure, prioritize daily duties and can be clear and concise when organizing and presenting data Sapphire offers very competitive compensation packages including bonuses and equity, as well as full benefit packages, which include health, dental, vision insurance, 401k, and paid time off. To apply, please send your CV and cover letter to human.resources@sapphireenergy.com and reference RA, Strain Evaluation in the subject. ]]>

<![CDATA[Sapphire Energy is a venture capital-backed company developing next generation biofuels based on recent advances in metabolic engineering. The company’s focus is the commercialization of high performance, low cost, and low carbon footprint biofuels that are direct replacements for conventional gasoline, diesel, and jet fuel. We are seeking an exceptional Chemometrics Scientist to join our Upstream Analytical Chemistry staff in San Diego, CA. Requirements: •A Ph.D. in chemistry, physics, engineering, or statistics, with 0-2 years of industrial chemometrics experience, or a lower degree with at least 3 years of relevant industrial experience. •A solid understanding of chemometrics is essential. This includes experience and fluency in Unscrambler software, data mining, visualization, and library design. •Strong knowledge of chemistry, chromatography, spectroscopy, and good lab technique. •Ability to develop codes and software to control multi-vendor hardware and customize instrumental software. •Due to the highly collaborative nature of this position, interpersonal and communication skills are extremely important. A short presentation will be required during the interview. •A comfort level with the fast-paced, changing, and stressful environment of a biotech start-up. •Ability to work independently and to collaborate in multidisciplinary teams. •Strong analytical and problem-solving skills and scientific creativity are essential. •Strong organizational, laboratory, and manual skills. •Demonstrated ability to independently design, execute, troubleshoot, and interpret experiments, and to build the appropriate chemometric models to rigorously analyze data. Responsibilities include, but are not limited to: •Collecting and assembling the most appropriate sample libraries •Designing and executing the appropriate experiments and calibrations. •Carrying out the relevant analytical chemistry experiments. •Building, analyzing, validating, and explaining chemometric models. •Producing written and oral reports of scientific work. •Working with client groups to identify and design the most informative and robust high-throughput screening assays. •Documenting, transferring, and training clients in HTS-chemometric methods Sapphire offers very competitive compensation packages including bonuses and equity, as well as full benefit packages, which include health, dental, vision insurance, 401k, and paid time off. To apply, please send your CV and cover letter to human.resources@sapphireenergy.com and reference Chemometrics in the subject line. ]]>

<![CDATA[DexCom, Inc., headquartered in San Diego, California, is focused on developing technology for the continuous monitoring of glucose in people with diabetes. DexCom is committed to developing technologies and products that improve the lives of people with diabetes. DexCom Inc. is currently adding a Supervisor, Microbiology to the Quality Assurance team. SUMMARY Responsible to ensure compliance to domestic and international standards with regards to the monitoring of environmental systems (i.e. HVAC/cleanroom, Compressed Air, Water), sterilization of medical devices, biocompatibility testing of materials, supervision and training of laboratory technicians. ESSENTIAL DUTIES AND RESPONSIBILITIES (may include other duties) • Supervise daily operation and testing requirements for the environmental monitoring program. • Establish and perform the environmental monitoring program for the Heating Ventilation & Air Conditioning (HVAC), Compressed Air and Pharmaceutical Grade Water Systems. • Supports process improvements by designing equipment, process and test method validations. • Establish and perform environmental monitoring program tracking and trending data base, data entry and quarterly reporting. • Establish and perform environmental monitoring excursion communication, reporting, investigation, disposition and corrective action process. Requires multi-department communication and approval for coordination of work performed (i.e. Operations, QC, Sanitization, Facilities and QA). • Assure compliance of the sterilization program for sterile implantable devices by performing scheduled re-qualification, supplier audits, new product qualifications, challenge and bioburden testing when necessary. REQUIREMENTS • Bachelor's degree (B.S.) from a four-year college or university; Microbiology or related field. • 3+ years of related experience. • Must have knowledge of the following 21 CFR 820, ISO 13485, CMDR, and EEC93/42, U.S. and • E.U. Pharmacopeia, International Organization for Standardization (ISO) 10993, 14644, ISO 14971 and other Risk guidance standards to create the processes and supporting documentation. • Additional Areas of possible competence: o Gamma, E-beam and ETO Sterilization, Biocompatibility of Materials, Cleanroom Microbiology o Solid understanding of international and domestic medical device GMPs/ Quality System Requirements o Solid understanding of international and domestic environmental monitoring requirements. o Develop and perform test method validations in support of microbiology operations (e.g. Endotoxin Testing) and interpret the results. About DexCom DexCom Inc. is a publicly traded company listed in the NASDAQ stock exchange. We have been FDA approved and commercially released two generations of continuous glucose monitors. More company information is available at www.dexcom.com. We offer an excellent benefits package including medical, dental, vision, life insurance and long term disability, 401(k), flexible spending account, a discounted employee stock purchase plan, paid time off, on-site fitness center, and a great work environment. If interested, please submit your resume to: hr@dexcom.com. Please include your salary requirements and reference ‘Supervisor, Microbiology’ in the subject line. ]]>

<![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a Sr. Lab Technician to work for a leading San Diego biotechnology company. Sr. Lab Technician The Sr. Lab Technician will assist with QC Chemistry testing of Biologic products. The position involves various tasks, including the performance of assays on in-process, final and stability products. The individual must demonstrate the ability to perform qualitative and quantitative assays by reading and following an SOP. The successful candidate should be proficient in conducting biological assays such as quantitative protein, radial immunodiffusion, isoelectric focusing and ELISA (various types). The Sr. Lab Technician will be tasked with reviewing current assays and revising them where necessary to improve outcomes. This includes revising the written SOP, so writing skills must meet this requirement. Having the capability and/or experience to design and execute laboratory validations is important. The Senior Lab Technician will maintain a stability test schedule and validation test schedules when necessary. This is a good position for an independent individual with 4 year degree in Biochemistry or a related science, and several years of specifically related experience. An advanced degree is desired. The position works along with the QC Chemistry Supervisor and reports to senior management for specific projects. Responsibilities: Perform testing of product: * Incoming materials used in production and laboratory * In-process, final and stability products * Sterility culture inspection Perform assay evaluation and validation * Conduct assays by following SOPs * Troubleshoot assay results and through experimentation, design assay improvements * Validate laboratory assays Stability scheduling * Perform associated tasks as needed SOP and protocol writing * Write/revise laboratory SOPs * Assist with validation protocol and report reviews Requirements: * BS in Biochemistry or related science with several years of specifically related experience. Advanced degree preferred. * Ability to work independently, for example, to pick up laboratory SOP and perform test. * Must have good writing skills Visit www.biophaseinc.com to view additional opportunities in San Diego County!]]>

<![CDATA[GMP PRODUCTION ASSOCIATE Background: PaxVax is an innovative and fast-paced vaccine start-up company developing candidate oral vaccines for influenza, and other key infectious diseases. The Company has committed funding of over $30 million to support its operations, with a fully operational lab and cGMP manufacturing facility, and our first vaccine is currently in a Phase I trial in the U.S. Summary of position: The Production Associate will be a key member of the Vaccine Production team reporting directly to the Director of Manufacturing and will be responsible for viral vaccine development, cGMP vaccine production, and cleanroom facility operations. Specific Responsibilities: • Bench and clinical scale process development for viral vaccine production • Mammalian cell culture and viral infection using aseptic techniques • Viral purification by chromatography and ultrafiltration • Lyophilization and/or spray drying development • Vaccine capsule/tablet preparation, including enteric coating development • cGMP manufacturing of clinical trial vaccine material • Author manufacturing SOPs, batch records, and material specifications Qualifications: • Bachelors of Science in Biology, Molecular Biology, or related discipline • Minimum of 2 years of biotechnology or pharmaceutical laboratory experience • Cell culture experience is necessary • GMP or GLP experience is desirable Contact: Please email resumes and interest to: hr@paxvax.com PaxVax is an Equal Opportunity Employer. PaxVax offers competitive compensation and benefits. No relocation assistance is available. ]]>

<![CDATA[CURRENTLY NO RELOCATION ASSISTANCE IS ATTACHED TO THIS POSITION. LOCAL CANDIDATES ARE PREFERRED AND WILL BE GIVEN PRIORITY REVIEW. Our client company has successfully integrated multiple disciplines, including chemistry, signal transduction biology, pharmacology and disease model biology, to build a highly-focused, cross-disciplinary team that rapidly generates small molecule kinase inhibitor drug candidates that will become the next generation of medical breakthroughs. They are currently seeking Research Associates, DMPK. Research Associate, DMPK Description: We are seeking a highly motivated individual with demonstrated abilities to design and execute in-house rodent based ADME, PK, and tolerability/toxicology studies. This position requires knowledge of drug metabolism and pharmacokinetic models and proficiencies in-life procedures. The primary responsibility of this position is to support the delivery of key ADME/T data to facilitate the goals of drug discovery and development projects through hands-on conduct of in vivo laboratory experiments. Minimum Requirements: MUST HAVE a four year scientific degree or veterinary technician certificate MUST HAVE 2-5 years relevant experience within pharmaceutical/biotechnology industry using DMPK techniques, etc. The applicant must possess strong organizational skills, a thorough knowledge of in-life technical procedures (e.g., animal handling, various routes of test article administration, and biological sample collections) and the ability to work independently. Strong verbal and written communication skills are requisite. NO PHONE CALLS NO THIRD PARTY RECRUITERS NO CONSULTANTS, PLEASE If you are interested in contributing to our exciting and collaborative organization, AND meet these minimum requirements, please forward a current resume by replying to our confidential Craigslist address (use reply button). THANK YOU! ]]>

<![CDATA[This position will be part of a dynamic, efficient customer service team. Will be primarily responsible for input online, phone, and fax orders and relative data into the ERP system. Responsible for responding and investigating to all customer inquiries regarding shipments, products and complaints. Responsible for answering incoming phone calls. Essential Functions: 1. Responsible for processing fax/email orders/phone orders 2. Main job focus will be to complete fax/email orders, and serve as a backup for our phone reps answering calls when necessary 3. Receive, investigate, and respond to all customer inquiries regarding shipments, products, and complaints 4. Process customer orders and revisions according to established company policies and procedures 5. Process customer returns according to established company policies and procedures 6. Follow up with customers when necessary to advise shipping delay and/or obtain additional information to process orders 7. Maintain composure and professionalism when handling irate customers 8. Cross train on other departmental duties to expand knowledge and skill set 9. Correspond with customers to solve any problems that may arise 10. Perform delivery checks on shipments when requested 11. Provide accurate information to customers regarding order status and product availability 12. Help facilitate marketing strategies that are implemented 13. Send out correspondence when necessary 14. Complete projects as assigned 15. Troubleshoot customer orders Skills and Qualifications: -BS degree in Biology or related field or Equivalent work experience in a Biotech company -Customer Service and/or Administrative experience required. -Must be detail oriented and have a high level of accuracy. -Must be able to follow instructions, and work within a team atmosphere meeting daily deadlines. -Must have the ability to multi-task and time manage multiple priorities and speak clearly and concisely in a professional manner. All interested applicants must apply and submit resume online on the Careers page of our website: www.biolegend.com ]]>

<![CDATA[Postdoctoral Fellow (VD-Shresta) A postdoctoral position is available in the Division of Vaccine Discovery at the La Jolla Institute for Allergy and Immunology (www.liai.org). The lab studies the immunology and virology of dengue virus infection by generating novel dengue viruses and using a reverse genetics approach and knock-out mouse strains. This position requires a Ph.D., and experience in virology, immunology, molecular biology, and working with mice is desirable. Projects involve investigating the role of antibodies, T cells, and the interferon system in dengue pathogenesis. For consideration, please send curriculum vitae and contact information of three references to: Sujan Shresta, Ph.D. Assistant Member Division of Vaccine Discovery La Jolla Institute for Allergy and Immunology 9420 Athena Circle La Jolla, CA 92037 email: sujan@liai.org ]]>

<![CDATA[Research Dietitian Profil Institute for Clinical Research, Inc. (“Profil”),is a private research institute based in Chula Vista, California. At Profil we are focused on early-phase clinical investigations (Phase I and II) of potential new treatments for Diabetes and other metabolic diseases. <a href="http://profil-research.com" rel="nofollow">http://profil-research.com</a> We are looking for a Research Dietitian who will participate in the development and implementation of the nutritional aspects of medical research studies and formulate subject diets in accordance with study requirements. Specific Responsibilities: Clinical Trials: 1. Interview subjects to determine diet history food preferences, and nutritional status including caloric intake and nutrient composition; review laboratory results as necessary; utilize computer assisted nutrient analysis 2. Assist in developing nutrition protocols; formulate diets in accordance with research protocol and subject nutritional needs; develop alternative diets based on subject preference, nutrient requirements, or medical conditions such as allergies 3. Instruct subject on nutritional aspects of study and evaluate compliance with protocol 4. Collect and evaluate data such as amount of food consumed and weight gain or loss, to maintain quality control and to detect changes induced by diet 5. Coordinate menus with caterer; evaluate appropriateness/accuracy of delivered meals 6. Develop and maintain QA program for food safety Staff: 1. Work in cooperation with the Project Management staff to assess protocol-specific dietary need 2. Coordinate research assistant staff in meal preparation and delivery Training: 1. Assist in training of research assistants in nutrition research and in the design and implementation of nutrition protocols 2. Make presentations to staff or subjects in nutrition or nutrition research Skills and Requirements Education Requirements/ Certifications: 1. Bachelors degree or higher in dietetics or food and nutrition. 2. Completion of American Dietetic Association approved dietetic education program Skills / Experience: 1. Two years experience in clinical dietetics or equivalent. 2. Excellent communication and supervisory skills 3. Familiarity with computer assisted nutrient analysis programs 4. Thorough knowledge and understanding of Good Clinical Practices 5. Knowledge of applicable FDA rules, regulations, guidance documents, governing conduct of human clinical trials At Profil, we offer a competitive and comprehensive salary and benefits package. If interested, please submit your resume to: hrpicr@profil-research.com ]]>

<![CDATA[Glasswash Technician needed for a Biotech company in Carlsbad! Description: • Responsible for recovering, washing, and drying glassware and distributing it to appropriate locations within the laboratory location(s). • Maintains glass washing facility and performs routine maintenance on glass washing equipment. • May sterilize glassware and other laboratory items in an autoclave. • Generally works on assignments that are semi-routine in nature, and requires ability to reorganize deviation from accepted practices. Primarily, the glasswash technician works on his/her own. However, the atmosphere in the company is one of camaraderie and support. To ensure happy working conditions for all staff, the incumbent in this role will need to think of him/her self as part of a team. Education/Experience Experience working in a cGMP environment a plus Requires a high school diploma or equivalent. Should have a minimum of 0-2 years' laboratory experience. Please send your resumes today!]]>

<![CDATA[Heidelberg Engineering is a high tech medical device company which designs, manufactures, and distributes diagnostic instruments for eye care professionals. The company’s products are used around the world by ophthalmologists and optometrists to scan patients’ eyes for signs of disease and to assist in the management of patients found to have disease. JOB SUMMARY: This person is responsible for regulatory submissions to FDA and international agencies for medical device clearance, approval and/or licensing as well as for clinical studies related to device. Works closely with others to prepare submissions for new products and product changes as required to ensure timely approval for market release. Interfaces with multiple functional areas, geographies and divisions within the company. This person will serve as the Corporate Compliance Officer. ESSENTIAL DUTIES AND RESPONSIBILITIES: • Prepares, reviews and submits necessary regulatory information to FDA to obtain 510(k) clearance and PMA approval of products. • Coordinates with various functional areas in the preparation, review and submission of IDE applications for clinical studies, as well as other clinical studies including marketing studies. • Reviews all submissions to FDA and international agencies for completeness, truthfulness and compliance with regulations. • Serves as the primary contact to FDA for review of submissions to FDA. • Keeps up-to-date on proposed regulations and guidelines published by FDA and international agencies. • Reviews advertising and promotional material and device labeling for regulatory compliance. • Controls the introduction of product through the United States market through management of the release approval process. • Initiates changes to practices and procedures to support compliance requirements • Brings regulatory and corporate compliance questions/issues to the attention of senior management • Provides general guidance or training support of professional staff. • Provides interpretations & direction to applicable company personnel regarding the regulatory aspects associated with relevant functions. • Acts as Corporate Compliance Officer to review, audit and ensure compliance with corporate compliance policies and procedures. KNOWLEDGE/SKILLS/ABILITIES REQUIRED: • Minimum of BS/BA in scientific or engineering discipline or equivalent combination of education and experience. MS or JD preferred. • 10-15 years of successful experience in related field and successful demonstration of increasing responsibility and accomplishment in the responsibilities described above. • Experience in the medical device industry preferred, but relevant experience in the area of combination products (drug/devices) will be considered. • Demonstrated excellent writing skills in the preparation of technical documents based on technical reports prepared by other technical functions. • A thorough understanding of U.S. FDA regulatory laws and requirements to ensure compliance to regulations without hindering business and growth and understanding of regulatory laws in major international markets. • High levels of professionalism, ethics and compliance in order to interact with FDA and serve as a representative of Heidelberg Engineering. • Strong written and oral communication skills in order to facilitate communications with FDA and minimize unnecessary FDA inquiries. • Advanced degree may be substituted for experience, where applicable. • Approximately 20% of time may require domestic and/or international travel. ** Position will require 1 week per month travel in Germany. • German language ability strongly preferred. ]]>

<![CDATA[Job Description Summary: This position is available for a motivated, flexible and responsible team player. The group aims to better understand the molecular determinants of kidney and cardiovascular function in diabetes and hypertension using gene-targeted mouse models. The group is associated with UCSD and the Veterans Medical Research Foundation (VMRF). The incumbent will perform, develop or adapt standard procedures like Western blotting, quantitative RT-PCR, biochemical analyses, maintenance of mouse breeding colonies, immunohistochemistry, and cell culture to meet the needs of research projects. Will acquire and apply knowledge and skills in the field of microsurgery and microanalysis in nanoliter volumina requiring excellent manual skills. May prepare charts and graphs involving experimental data and co-author scientific journal articles. Qualification Summary: Bachelor's degree in Molecular Biology, Biochemistry, Biology or related field; or at least one to two years related experience and/or training; or equivalent combination of education and experience. Experience in the outlined procedures. Excellent manual and pipetting skills. Motivation to work in a team toward high quality research for publication.]]>

<![CDATA[BPS Bioscience Inc., headquartered in San Diego, California, is focused on developing recombinant enzymes and enzyme assay kits for drug discovery. BPS Bioscience Inc is committed to developing products that accelerate the drug discovery for treatment of human diseases. BPS Bioscience Inc. is currently seeking a Research Associate. Description We are seeking an exceptional biochemist, with a strong background in enzymology, enzyme kinetics, and enzyme assay development. This individual will closely work with Sr. Scientist to develop enzyme assay and ensure the quality of products. This successful candidate will be responsible for enzyme characterization, assay development, enzyme kinetics and high through-put screening of small molecule inhibitors. Requirements A Bachelor or Master of Science degree in Biochemistry, Molecular Biology, Cell Biology, Biophysics, or a related field is required. Must have proven ability in enzyme assay development, protein characterization, enzyme kinetics and mechanistic studies. Use of bioinformatics and statistics for the analysis and visualization of large data sets is a plus. Strong teamwork, organizational skills, and written and oral communication skills, are essential. ]]>

<![CDATA[We are a biotech company that provides antibodies and cell culture products to universities and biotech/pharmaceutical companies worldwide. We are seeking a highly motivated technician to work with our antibody and kit development team. The qualified technician’s responsibilities will include, but are not limited to: antibody characterization, cell culture, inventory, creating product datasheets. Techniques used will include Western Blotting, cell culture, immunoprecipitation, immunocytochemistry, and affinity purification. Familiarity with the above techniques, the Windows Office software suite, and Photoshop are preferred. Requirements: B.S. degree in cell biology and/or biochemistry/Immunology, and some knowledge of signal transduction. To apply for the position, please submit your resume/CV via email, including "Antibody Technician 1003" in the subject line.]]>

<![CDATA[Predictive Biology is a startup stage biotech company developing mouse embryonic stem cell lines for biomarker discovery. A Research Associate II or Research Scientist position is currently available. Must be highly motivated and willing to take on a broad range of responsibilties in a start up company setting. For more information, visit www.predictivebio.com. RESPONSIBILITIES include: Develop and maintain large numbers of mouse ES cell lines. Characterize ES lines using FACS and molecular technologies. Develop and conduct functional assays with ES cell lines and differentiated cell populations. MINIMUM QUALIFICATIONS include: B.A./B.S. with 8+ years of mammalian cell culture experience, or M.S./PhD with 5+ years of mammalian cell culture experience. Extensive tissue culture experience is essential, and embryonic stem cell culture experience is highly desirable. Experience with FACS, DNA/RNA isolation, qPCR assays (e.g., taqman) is required. Highly organized, with meticuluous attention to tracking experimental details. Able to work independently and communciate clearly and effectively with others. ]]>

<![CDATA[Stantec's Environmental Management team, armed with scientific knowledge of air, water, and soil, creates sustainable solutions and addresses regulatory permitting and compliance for our clients. Our involvement on projects can extend from developing initial project concepts and environmental approvals to site decommissioning, remediation, and reclamation. The services our team provides are diverse—ranging from endangered species monitoring to landfill design, from groundwater studies to dam assessments and design, from archaeological studies to contaminated site cleanup, and from managing large-scale environmental assessments for the energy and power sectors to GIS and information management. In today's increasingly competitive global market, excellence in environmental management can enhance the reputation and position of a company within its industry. At Stantec we specialize in the environment. We manage environmental issues professionally and proactively to improve our clients' profitability and competitive advantage by allowing them to identify and respond to opportunities and threats within the changing regulatory and corporate environments. Responsibilities: • We're currently looking for a Biologist to conduct biological surveys for Salt Marsh harvest mouse and to conduct construction monitoring in the field for pipeline projects. • This position can be located in San Diego, Bakersfield, Sacramento, San Francisco or Fresno. Projects are located throughout California and the western U.S. Up to 50% travel is required. • Hours will fluctuate between 15 - 40 hours a week initially. As workload increases, we anticipate this position becoming full-time working 40 hours a week consistently. Qualifications: • Must be a Qualified Biologist (hold a Bachelor's degree in biology from an accredited college) with 3 - 5 years experience, specifically conducting biological surveys for Salt Marsh harvest mouse and conducting construction monitoring in the field for pipeline projects. • Must have Northern California work experience. • Candidates should have a solid background in wildlife, taxonomy, and/or botany, with some exposure to sampling protocols and field project logistics. • Superb observation skills are highly valued, as are a keen interest in ecosystems, comfort with computers and technology, a willingness to learn new skills while conducting fieldwork in rural or wilderness settings, and flexibility in work assignments. • The ability to develop basic reports from field notes is essential. To keep accurate field notes, photo logs, use GPS, etc for use in report preparation. • Ability to work in teams or alone in the field • A willingness to work long hours in the field • Flexibility in work assignments - location and type of assignments will vary. • Resume would have to be approved by US Fish and Wildlife as a condition of employment or the candidate would have to hold a scientific collection permit for the above listed specie. • Additional experience with California Clapper rail or northern California aquatic flora and fauna would also be helpful. Stantec offers an excellent benefits and compensation package including medical, dental, vision, 401(k) matching, wellness program, paid vacation and holidays, stock purchase plan, commuter flex-pass, and pre-tax health plans. To apply for this position, go to: <a href="http://jobs-stantec.icims.com/jobs/8810" rel="nofollow">http://jobs-stantec.icims.com/jobs/8810</a> Stantec Consulting Inc. is an equal opportunity employer. For more information, click www.stantec.com. ]]>

<![CDATA[Kelly Scientific Recruiter posting: Every day Kelly Scientific Resources connects scientific professionals with opportunities to advance their careers. We currently have an exciting internal opportunity to work as a Scientific Recruiter at our San Diego Kelly Scientific branch. This is an excellent opportunity for individuals with a scientific background, great communication skills, and a solid work ethic. The Scientific Recruiter will be responsible for working with clients in the pharmaceutical, nutraceutical, biotech, medical device, and other industries with science related positions. The main function is to partner with each company, gain an understanding of their goals, and provide candidates that match the required skill set. The Recruiter will source top talent by utilizing job boards, networking events, local campus recruiting, scientific organizations, referrals, and several other methods. Responsibilities include but are not limited to: Sourcing, screening, qualifying, hiring, and assigning qualified candidates to positions Account and employee management Use resume databases, local Universities, local scientific organizations, and job fairs for recruiting candidates and generating leads Have industry knowledge for recruiting positions such as biomedical, biotech, pharmaceutical, clinical, chemical, and manufacturing. Conduct phone screens and in-person interviews daily Submit background screens Coordinated interviews with candidate and client Completed the Kelly standard hiring process accurately Assist with branch operations Minimum Education/Experience Four year degree in a scientific discipline Experience in recruiting, an industry scientific role, or sales ]]>

<![CDATA[Summary GenWay Biotech is seeking a part time sales assistant to promote the You Test You™ Cancer Assessment (www.youtestyou.com). This position would communicate directly with San Diego organizations and customers and inform them of our test offering. We are seeking someone who can work 20 hours per week. Approximately 50% of time will be out in the field and the other 50% will be administrative duties at GenWay’s office. Position pays $15/hour. Driver’s mileage will be reimbursed. There will be additional opportunities to grow and progress in your career. Responsibilities • Have a strong technical knowledge of You Test You™ Cancer Assessment • Set up meetings with large institutions • Identify and communicate to local San Diego organizations • Prepare fliers and marketing materials for events • Enter lead information into a CRM • Obtain feedback from the field Knowledge and Skills Required • Polished presentation skills • Some scientific knowledge • Prior sales experience • Effective project management • Detail-oriented with strong organizational skills to handle a variety of tasks. • Excellent communication skills essential • Initiative, drive, common sense, creative flair, and flexibility are essential • Strong working knowledge of Microsoft Office products ]]>

<![CDATA[We have an immediate opening for a motivated, driven QC Associate, in a dynamic Research and Development department in a rapidly growing, international, biotech company! This position will be primarily responsible to perform under supervision essential functions related to the flow cytometry testing of antibodies through surface, intracellular, and multicolor analysis. Responsibilities include, but are not limited to: carrying out the flow cytometry testing, data acquisition and analysis, following SOP and the QC Specification for each lot release, stability testing, ensuring data accuracy, cell culture and buffer preparation. -Minimum BS in Biology, or related study, + 1-2 years lab experience -Must be proficient in statistical techniques for data summary and analysis -Must have experience with experimental design and knowledge of computer software -Knowledge and experience with flow cytometry and cell culture preferred -Should have good organization and communication skills -Strong attention to detail, dependability, ability to work in a team are all necessary to be a successful candidate All interested candidates must apply and submit resumes online on our Careers page on the website: www.biolegend.com ]]>

<![CDATA[Position: Senior Manager, Quality Control March 8, 2010 Tocagen is seeking a Senior Manager, Quality Control, who will be responsible for the development, implementation, performance, validation and maintenance of both Tocagen’s internal and external Quality Control (QC) activities to include: (1) monitoring performance of external QC and manufacturing contract activities; (2) the set-up and maintenance of a separate and dedicated internal QC laboratory area and (3) the interaction with European QPs to release clinical material for European clinical trials. He/she will be responsible for scheduling the performance of routine and non-routine external and internal product specific testing for “in process”, and “finished” GMP, as well as Pre-Clinical product according to established SOPs. The Senior Manager, Quality Control will also be responsible for coordinating, documenting and executing assay validation activities, as well as setting up testing data bases and assuming responsibility for all relevant testing documentation for each defined production lot. The Senior Manager, Quality Control may also perform special projects and be expected to deal with analytical and instrument problem solving, as well as to apply his/her knowledge of GMP and GLP in day to day activities, including compliance activities with all relevant FDA, EMEA and ISO requirements. The Senior Manager, Quality Control will recommend and implement corrective actions and prepare deviation reports as necessary to ensure consistent adherence to the organization’s quality program. Major Responsibilities include: • Sets and meets yearly and monthly goals for QC group to support manufacturing, regulatory and company goals • In conjunction with Senior Director of Product Development and Manufacturing, develops annual budget for QC function according to overall company plans and priorities • Plans, coordinates, directs, performs and documents internal and external activities for Tocagen’s quality control program to allow production and release of clinical products consistent with established standards and procedures • Trains and supervises QC analyst(s) in the performance of product testing procedures • Monitors outside contractors for compliance with Tocagen requirements • Manages, with Assay Development, the transfer of product assays from Assay Development to Quality Control and is responsible for overall assay validations • Reviews and analyses product specifications, test trends and deviations, in cooperation with other Tocagen functional groups, to maximize product reliability and meet company goals • Organizes training activities related to product quality and reliability, and ensures the calibration and maintenance of laboratory equipment • Writes validation protocols, QC deviations and reports for analysis methods • Performs special projects as required, including analytical and instrument problem solving. Experience and qualifications include: • Requires a Bachelors, Masters or PhD. degree in a scientific discipline (Biochemistry, Microbiology, etc.), with a minimum of 5 years as a QC or QA laboratory supervisor experienced cell based, q-PCR and HPLC based test methods • Knowledge of good manufacturing practices (GMP's), good laboratory practices (GLP's), USP testing methods and statistical processes as described in FDA regulations, ICH guidelines, and EMEA guidance’s • Previous experience with biological vaccines and/or other recombinant biological type products required • Minimum of 5 years of supervisory experience in a biopharmaceutical GMP environment working with outside manufacturing and QC contractors, preferably with a commercial product, or in a large biopharmaceutical company context. • Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures and governmental regulations • Ability to write reports, business correspondence and procedure manuals; ability to communicate effectively regarding the status of QC testing of materials produced as applicable to the planning/inventory schedule • Ability to apply standard mathematical and statistical methods (such as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory and factor analysis) to support interpretation of test results • Able to think strategically, negotiate and influence effectively, understand complex technical issues and be able to translate and communicate them clearly to less technical personnel • Strong collaboration, team building, and people development skills a necessity Compensation and reporting: • This is an exempt position reporting to the Senior Director of Product Development and Manufacturing • Salary is negotiable commensurate with experience and fit for position • Tocagen has a highly competitive health and welfare benefits package Contact: • Please e-mail professional CVs to info@tocagen.com. Further information regarding Tocagen can be found at www.tocagen.com ]]>

<![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a Sr. Engineer, Fermentation to work for a leading San Diego biotechnology company. Sr. Engineer, Fermentation ESSENTIAL JOB FUNCTIONS: * Oversees all large-scale plasmid DNA and protein production, particularly as it pertains to fermentation and harvest. * Implements complex production and manufacturing procedures. * Optimizes processes. * Reliably executes SOP’s and Batch Records. * Writes SOP’s and Batch Records. * Initiates revisions to current GMP/SOP guidelines. * Accurately documents and analyzes data and presents conclusions. * Ensures routine maintenance of production equipment is performed. * Assists other technical personnel on issues and problems. * Manages assistants and associates on production procedures. * Responsible for scale-up and troubleshooting of manufacturing processes. * Coordinates with Process Engineering in the development of scalable processes with improved product yield and reduced costs for manufacturing systems. * Researches and implements new methods and technologies to enhance operations. Suggests improvements to existing methods and procedures. * Performs literature search on topics provided. * Produces complex, high-level materials using established procedures and protocols. * Maintains cGMP environment to support regulatory compliance. * Ensures disposal of lab wastes according to established procedures. * May oversee lyophilization programs including implementation and tech transfers. * Complete other duties as assigned by supervisor. JOB SPECIFICATIONS: * Bachelor’s degree in a Life Sciences discipline or equivalent. * Eight to ten (8-10) years relevant experience in manufacturing. * Demonstrated ability to understand and apply complex technical concepts to manufacturing/production methodology. * Detail oriented and strong written and verbal communication skills. * Ability to work independently, within prescribed guidelines, or as a team member. * Demonstrated ability to follow detailed directions in a laboratory environment. * Must be familiar with Microsoft Office applications. Please also visit <a href="http://www.biophaseinc.com" rel="nofollow">http://www.biophaseinc.com</a> to view additional opportunities in San Diego County!]]>

<![CDATA[Dear CRAs, One of San Diego's best biotech companies to work for is seeking an on site CRA to join their team. Please submit your resume and references as word document if you are interested in applying. Clinical Research Associate II-IV Direct Hire/Permanent Position Job description: • Conducts site-monitoring visits and activities accordance with CFR regulations, ICH/ GCPs guidelines, departmental SOPs and Work Instructions and the Clinical Monitoring Plan. • Ensures conduct and records are complete & consistent with governing regulations. • Able to use or Uses eCDM and other tools to review monitor listings and queries. • Conducts site initiation monitoring visits and trains site personnel. • .Assists sites with site-level IRB submissions, queries and documentation. • Works with Clinical Operations Manager to administer subject recruitment incentive, and retention programs at the sites. • Establishes and maintains regular communication with clinical sites. • Conducts interim site monitoring visits including document review, accurate data recording, source data verification, protocol adherence, study material accountability. • Prepares and maintains monitoring records such as trip reports, corrective actions, telephone logs, and communications files. • Resolves routine site issues, protocol deviations, queries and study discrepancies; identifies and gathers missing or incomplete data. • Resolves non-routine site issues in conjunction with the Clinical Operation Manager • Ensures distribution, collection, and tracking of regulatory document to ensure site compliance and audit readiness. • Conducts closeout monitoring visits including reviewing record retention requirements and disposition of study supplies. • Assists in reviewing draft tables and listing output for the clinical study report. • Ensures complete & accurate data collection, QC, & record keeping • May assists in the validation and QC of clinical study database(s). Job Requirements: • BA or BS and 3-5+ years related experience • Working knowledge of clinical trial practices and regulations. • Working knowledge of clinical monitoring and trial design. • Working knowledge of clinical trial databases. • Familiarity with the application & implementation of basic statistical analysis methods as they apply to clinical trials. • 30-50% travel will be required.]]>

<![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a Research Associate, DMPK to work for a leading San Diego biotechnology company. Research Associate, DMPK We are seeking a highly motivated individual with demonstrated abilities to design and execute in-house rodent based ADME, PK, and tolerability/toxicology studies. This position requires knowledge of drug metabolism and pharmacokinetic models and proficiencies in-life procedures. The primary responsibility of this position is to support the delivery of key ADME/T data to facilitate the goals of drug discovery and development projects through hands-on conduct of in vivo laboratory experiments. Minimum Requirements: Requires a four year scientific degree or veterinary technician certificate with a minimum of 2 years relevant experience in pharmaceutical/biotechnology industry. The applicant must possess strong organizational skills, a thorough knowledge of in-life technical procedures (e.g., animal handling, various routes of test article administration, and biological sample collections) and the ability to work independently. Strong verbal and written communication skills are requisite. Please also visit <a href="http://www.biophaseinc.com" rel="nofollow">http://www.biophaseinc.com</a> to view additional opportunities in San Diego County!]]>

<![CDATA[La Jolla Institute for Allergy & Immunology (www.liai.org) Please apply directly to: careers.liai.org/applicants/Central?quickFind=50360 We are preferably looking for someone who has experience working with laboratories or biotechs and more specifically a NIH biosketch or grant. The Research Administrative Assistant is to provide administrative and secretarial support to assigned PI’s/Divisions. Several functions are to be accomplished by working in close conjunction with administrative staff/departments and adhering to Institute policies and procedures. This position may also support Faculty and/or Administrative Staff in performance of assigned institutional duties. Essential Duties & Responsibilities Lab Division Duties: General: • Compiles information, prioritizes and coordinates various projects as requested by assigned PI’s/Divisions. • Processes mail and faxes, screens phone calls, maintains appointment calendars, organizes meetings, set-up and maintain administrative files (inventory, personnel files, correspondence, etc.) and interacts regularly with staff and outside contacts. • Prepares check requests, expense reports, and other administrative forms in accordance with Institute policies and procedures. • Maintains reprint (PDF) files and processes reprint requests accordingly. • Maintains journal subscriptions and society memberships. • Maintains various databases to help facilitate grant writing (i.e. EndNote bibliographies, Pubmed Central, Pubmed, and other journal “alert” notifications.) • Assists with preparation of manuscripts. • Assists with editorial work for scientific journals and books. • Makes travel arrangements for Division Head, Associate or Assistant Members, and research staff. This includes registration, airfare, hotel, transportation, and itineraries, processing reimbursements, reconciling travel accounts and maintaining accurate files. • Makes travel arrangements/accommodations and meeting schedules for visitors (i.e. collaborators, prospective postdoctoral fellows, etc.) • Helps coordinate travel with seminar speakers invited by supporting labs in conjunction with seminar program coordinator. • Organize scientific conferences and events. • Assists with organization of Division social functions (i.e. birthday or other special celebrations, recognition of funding received and recognition of publications, Happy Hours, etc.) • Responsible for ordering office supplies for laboratory areas. • Provides administrative and secretarial back up to other Divisions as necessary. • Completing administrative forms as requested from other institutions that are associated with adjunct professorship appointments, etc. • Prepares and submits Requisitions to engage Research Consultants to the Manager of Sponsored Research. Sponsored Research: • Serves as a liaison between the Research Administration Office and the individual Research Divisions. The overall goal of this teaming is to facilitate efficiency in LIAI’s pre-award program for extramural research grants, contracts and fellowships. • Assist in completing and submitting all necessary protocols to appropriate LIAI committees (IRB, IBC, ACC) and maintaining record of current protocol numbers. • Prepare/maintain CV’s and biosketch documents for division research staff. • Collects biosketches from all key personnel, significant contributors and/or consultants, following specific timeline provided by OSR. • Final assembly of applications: completion of table of contents, inclusion of scientific portion, page numbering and biosketches. • Makes copies of grant applications and mails to funding agency on or before submission deadline (exception is electronic submission of NIH grants.) • Makes necessary copies of submitted grant applications for Research Administration, Vivarium and Bio Safety to assure appropriate award tracking and reporting. • Maintain PI files on each pending, funded, and terminated grants for specific divisions. • May assist in monitoring due dates of grant applications and progress reports; the primary responsibility for this resides with OSR. • If designated by the PI, may review funding and spending patterns of accounts with OSR and Accounting for review with PI’s (i.e. monthly animal charges, supplies purchasing) and maintenance of current grant accounting numbers. Intellectual Property: • Assists faculty with material transfer agreements (provide IP with third party agreement, enter request online, etc.) Leveling Requirements High School diploma or equivalent. Minimum of 2 years experience in a secretarial/administrative scientific environment. Ability to prioritize and balance numerous tasks with minimal direction to meet deadlines, and work independently and be proactive. Strong interpersonal and communication skills, with the ability to work with Institute personnel and outside contacts in a professional manner, maintaining confidentiality of sensitive information. Ability to exercise flexibility, tact and good judgment. Accurate and fast work processing skills, familiarity with a Macintosh computer, graphics and other programs, and ability to utilize new software. Understanding of the Institute’s goals, objectives, policies and procedures. Ability to coordinate and delegate responsibility for part-time support to meet Research Administration goals. Please apply directly to: careers.liai.org/applicants/Central?quickFind=50360]]>

<![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a Manufacturing Operator to work for a leading San Diego biotechnology company. Manufacturing Operator Essential Duties & Responsibilities: * Perform manufacturing tasks as operator or verifier in the production of human mesenchymal stem cells (hMSC) and other cell related cell lines including; media preparation, cell seeding, media change, harvest, aliqouting and freezing of intermediate and final product. Manufacturing tasks require the manipulation of large numbers of petri dishes and T-flasks in an aseptic environment. * Process tissue specimens for isolation of hMSC and other cell sources. * Read, comprehend, and adhere to standard operating procedures (SOPs). * Complete and review GMP documentation (Batch Records, Forms, Charts). * Perform routine and advanced duties required to clean, maintain and operate equipment. * Perform basic troubleshooting and communication of floor and production observations to supervisory staff. * Proficient and fully trained in clean room gowning and aseptic technique practices. * Participate in all departmental Aspetic Process Simulations (APS) medium qualification requirements. * Document and maintain training records for read and understand and on the job training (OJT). * Stock production and gowning areas as required. * Maintain and review area charts and SOP binders. * Assist in maintaining the production areas and records in an inspection ready state at all times. * Train newer staff on GMP and technical tasks, operations and SOPs. * Author or assist in drafting and revising of departmental procedures and practices. * Interact with vendors to provide current equipment, components and best practices to the process. * Adhere to all EH&S policies, procedures and guidelines. Education and Experience: A BS or BA in biology or equivalent is required, however exceptions may be made based on relevant industry experience. A minimum of 2 year of industry experience in the cell therapy or a closely-related industry required. Please also visit <a href="http://www.biophaseinc.com" rel="nofollow">http://www.biophaseinc.com</a> to view additional opportunities in San Diego County!]]>

<![CDATA[BUYER/MANUFACTURING ADMINISTRATOR Medical Devices – Local candidates only BeneChill, Inc., a medical device company in San Diego, has an immediate need for a Buyer/Manufacturing Administrator with experience in the biotech industry. The company offers an excellent compensation package and great benefits. Position Summary Position will report directly to the Quality & Logistics Manager. The Buyer/Manufacturing Administrator shall be responsible for the administrative and office support activities for Purchasing, Quality, and Manufacturing. Key Duties and Responsibilities include the following:  Sourcing prospective suppliers and initiating the supplier qualification process.  Placing purchase orders for manufacturing supplies and/or inventory parts.  Tracking and closing open purchasing orders.  Following up on supplier corrective action requests. Resolving non-conformances with suppliers and assuring correct materials are received.  General office management and administrative support.  Data entry for Inspection activities and Document Control Support.  Assisting in material requirements planning (MRP) and inventory planning, as needed.  Assisting the Quality Manager in the day to day operations of Quality and Logistics.  Generating labels and filing manufacturing records. Required Education • AA degree required, bachelor’s degree preferred. Required Experience • Minimum 4 years of work experience in the medical device industry. • Minimum 3 years in purchasing/manufacturing function. Other Requirements • Must be a self motivated, innovative, results oriented team player. • Must have excellent verbal and written communication skills. Must be computer literate. • Must be fluent in MS Office (MS Word, Excel) Please respond to by attaching your resume to the email address: hr@beneChill.Com and someone will give you a call if you meet the requirements. ]]>

<![CDATA[Major responsibility of the position is the synthesis of custom DNA oligonucleotides according to the company's Standard Operation Procedures (SOPs) and Quality Control Criterion (QCC). Other job responsibilities include basic administrative work as well as product packaging and preparation. BA/BS degree in chemistry/biology or related fields, requires basic biology lab skills and computer skills (e.g, MS word, MS excel, etc). Work hours between 3:30 pm to 12 midnight M-F or M-Th and Sun.]]>

<![CDATA[Large Biotech Company in the Sorrento Valley area has an immediate need for a Production Chemist! *This is a full time, M-F, 7am to 3:30pm, temp to hire position* The pay rate is $15-20/hour DOE QUALIFICATIONS: * MUST have a B.S. degree in Chemistry. ** Only a B.S. in Chemistry will be considered for this position* *Must have manufacturing and Oligo experience* DUTIES: * Synthesize and purify scheduled quantities of DNA, AE labeled probes according to written manufacturing instructions and standard operating procedures to ensure that quality specifications and schedules are met. * Enters inventory and labor charges into the MRP system. * Assist in ensuring the department meets all applicable QSR and ISO 9001 regulations. * Develop and implement manufacturing documentation and standard operating procedures to ensure product uniformity, reproducibility and compliance with QSR regulations. * Maintain supplies of materials/reagents required to meet manufacturing schedules. * Alert supervisor of any material shortages, equipment requirements, or other circumstances which may cause delays in the planned manufacturing schedule. * Interface with OTS Oligo Dev personnel to learn production procedures for new products and to successfully oversee the transfer of knowledge and techniques to the Probe Manufacturing Department. * Maintain laboratories, working areas and equipment in a clean and functional state in order to comply with current federal QSRs. REQUIREMENTS: B.S. degree in Chemistry. Two years of directly related laboratory experience including DNA synthesis, HPLC purification, electrophoresis and solution preparation, preferably in a regulated environment. Good working knowledge of chemistry, biochemistry, laboratory and safety, mathematics, and federal QSRs. Demonstrable skills in verbal and written communications in English are required. Please email your resume today!]]>

<![CDATA[BE A LEADER! Dexcom is seeking a Project Manager who will lead detailed project(s) from concept to commercialization. This position requires a strong understanding of product development process and medical device design control requirements in the medical device industry. The Project Manager is expected to be able to manage several projects with limited supervision or moderate guidance and coaching. Manage complex projects from concept to commercialization, working closely with Clinical Affairs and technical lead. Responsible for compliance to medical device design control Design History File (DHF) and product development process for all aspects of program. Coordinate activities/tasks and resources across all departments including Clinical Affairs, Marketing, Technical team, Quality, Regulatory Affairs, and Operations. Develop, track and report on program plan, detailed project schedule, clinical trials status, change control requests, and program deliverables. Liaison to corporate partners as necessary. Communicate program status to management, cross functional teams and have the ability and confidence to run design review and other key meetings. Qualifications • B.A. or B.S. in science, business, engineering, or equivalent technical field is required. • 4-5 years of relevant work experience in medical device or pharmaceutical industry a must. • In-depth knowledge of the product development process and medical device design control requirements is required. Working knowledge of GMP’s and ISO standards. • Demonstrated successful management of a complex program is required. • Proficiency in Microsoft Office, Microsoft Project, and Visio is required. • Program Management certification, i.e. PMP or equivalent, is preferred. • Excellent communication skills with the ability to convey technical and business information clearly and effectively through informal and formal documents, reports, and presentations to senior management. About DexCom, Inc. DexCom Inc. is a medical device manufacturer pioneering the field of continuous glucose monitoring for persons with diabetes. DexCom Inc. is a rapidly growing, dynamic, innovative company that prides itself on offering persons with diabetes with the best, most innovative technology in the field of continuous glucose monitoring. We are a growing company with approximately 280 employees, where each individual can be a great contributor. DexCom Inc. is a publicly traded company listed in the NASDAQ stock exchange. More company information is available at www.dexcom.com We offer a competitive benefits package including stock options and a discounted employee stock purchase plan. Please submit your resume to HR@dexcom.com; please reference “Proj Mgr” in the subject headline. ]]>

<![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a Research Scientist I to work for a leading San Diego biotechnology company. Research Scientist I Description: Responsible for the development, implementation, trouble-shooting and transfer of diagnostic products to the clinical laboratory. Requirements: * Develops ideas leading to new experimentation * Performs complex searches of databanks, isolates pertinent information and presents results in team meetings * Maintains up-to-date knowledge of scientific literature pertinent to ongoing projects * Assesses novel technologies for biomarker identification and/or diagnostic testing * Develops and implements novel data analysis methods * Conducts scientific studies to develop clinical assays leading to the marketability of clinical laboratory products * Maintains pertinent knowledge of state-of-the-art scientific principles and theories related to the company's development projects * Conducts transfer of R&D assays to Operations * May serve as an informational consultant to internal departments * May provide scientific guidance for technical staff engaged in assay development * May participate in organizational project teams We are seeking only local candidates at this time. Please also visit <a href="http://www.biophaseinc.com" rel="nofollow">http://www.biophaseinc.com</a> to view additional opportunities in San Diego County!]]>

<![CDATA[Leading biotech company in Mira Mesa seeks an Associate Scientist. This is an exciting and challenging position in the production department. The Biosciences production team makes a multitude of products. Working under limited supervision, this position must possess independent judgment and the ability to enhance existing processes. Techniques include but are not limited to ELISA and bead based assays. Other responsibilities may include, but are not limited to: Complete documentation according to department specifications Perform all SAP software functions necessary to support manufacturing Ensures products are manufactured and delivered in a timely fashion Lead process development and troubleshooting projects Write and revise SOPs, protocols, and work instructions Assist in general laboratory maintenance Minimum of 7 years hands on experience required Please submit your resume as a Word attachment for immediate consideration. Please note that this is a contract position for several months. ]]>

<![CDATA[Description This position primarily supports the Quality Assurance activities of the company. This individual would possess and maintain a basic knowledge of chemistry and should be familiar with techniques employed in an analytical laboratory setting ( Karl-Fischer titrations, Gas Chromatography, use of inert environment glove boxes, ICP instrumentation a plus, etc). Daily contacts are primarily limited to departmental personnel. Plans and schedules some of his/her own work. 8:00 am - 5:00 pm schedule but HM is flexible. Will A Drug Screen Be Required For This Position? Yes Will Position Require a Fit for Duty Evaluation? (Check Department/Job Requirements) Yes *This is a 1 year contract position. *If interested, please send the most updated copy of your resume. ]]>

<![CDATA[Plant tissue culture laboratory is looking for experienced plant tissue culture technician. Applicants should have experience in the following: Initiation of explants Transfering of sterile cultures Build up of mother stock cultures using sterile technique Knowledge of how to use of plant hormones to induce plant growth in vitro Great note taking skills Great organizational skills Ability to work independently ]]>

<![CDATA[PROVEN Staffing has an immediate opening for a Research Associate/Lab Assistant experienced in biology or chemistry for a part-time/contract position in the Drug Metabolism group. Experience with quantitative bioanalysis using LC-MS/MS systems for the the analysis of small molecules, conducting in vitro metabolic stability, cytochrome P450 and other DMPK assays is a plus. The ability to manage work independently while working effectively in a team is required. This position is 20 hours/week, flexible on the schedule but has to be between the hours of 8-5. No weekends or after hours work available. Contact Darryl Taylor at dtaylor@proveninc.com for immediate consideration.]]>

<![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for an Microbiology / Molecular Biology Project Manager to work for a leading San Diego biotechnology company. Responsibilities include, but are not limited to: * Collecting of project plan updates, maintenance or modification of project plan documentation and the preparation of project reports. * Assisting executives in the identification and scheduling of deliverables, milestones, and required tasks, and establishing standards for project reporting and documentation. * Assisting with detailing scientific programming with researchers and operations staff, including record keeping, meeting schedules, tracking weekly action items and other project management tools. * Preparing briefs and presentations. * Work with the Operations to coordinate operational and support services, including training for scientific staff in the general use and function of designated equipment and providing technical input to purchasing and other functional areas as required. * Maintenance of SOPs; working with Legal to document manage SOPs. * Tracking all project intellectual property status; working with legal to ensure document management and application deadlines. * Working with Corporate to schedule facility visits, tours, and education outreach events involving science staff. * Assisting EH&S with preparing and conducting training, coordinating safety training using outside resources, updating safety policies, and ensuring safety compliance of Company personnel. Requirements: * MS or PhD in biological sciences or related field, a minimum of 2 years laboratory experience, and a minimum of 2 years of applicable administrative or organization experience. * Must be familiar with Microsoft Office programs, in particular Outlook and PowerPoint. * Ability to work cooperatively and strategically in a team environment with all levels of professional, technical and administrative staff. * Must have excellent organizational and problem solving skills. * Comfort with leadership & accountability. Also, visit <a href="http://www.biophaseinc.com" rel="nofollow">http://www.biophaseinc.com</a> to view additional opportunities in San Diego County!]]>

<![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a Research Associate II to work for a leading San Diego biotechnology company. Research Associate II Assists with the development of diagnostic assays and analytical methods for the transfer of technology to the Clinical Laboratory in an interdisciplinary R&D department. ESSENTIAL DUTIES AND RESPONSIBILITIES * Performs experimental procedures from written SOP's * Assists in the development of new assays * Contributes to the improvement of existing assays and in the development of new tests. * Assists in the analysis of data utilizing Microsoft Access, Excel and other graphing programs. * Maintains databases as needed * Performs experiments utilizing molecular biology procedures such as nucleic acid extraction, PCR, RT-PCR, and hybridization assays * Performs experiments utilizing immunological procedures such as immunostaining, immunoassay and Western Blot techniques * Assists with assay transfer to the Clinical Laboratory * Maintains and troubleshoots research instrumentation and suggests upgrades as required * Confers with department staff regarding research and prepares research summaries * Assists in research and evaluation of new technologies EDUCATION and/or EXPERIENCE Position generally requires a bachelor's degree (B.A./B.S.) in the biological sciences from four-year college or university; with 2-5 years research and/or laboratory experience or a M.S. degree with 0-2 years of research laboratory experience in molecular biology and/or immunochemistry experience and must have hands on experience in performing immuno- and nucleic acid assays, and preparing reagents and/or analytical chemistry and instrumentation experience (e.g., HPLC). Experience in working in GLP/FDA/CLIA regulated atmosphere preferred. Local candidates only will be considered at this time. If you are not local but plan to relocate, please let us know. Be sure to visit <a href="http://www.biophaseinc.com" rel="nofollow">http://www.biophaseinc.com</a> to view all our latest job opportunities. ]]>

<![CDATA[Biochemist Associate part time position available for dedicated research project. A minimum of a B.S. degree essential. Attention to details and excellent communication skills required.]]>

<![CDATA[You will manage chemical information about commercially available compounds. Users of the system are research scientists in the life science industry and academic institutions worldwide. You will work with chemical suppliers, mostly screening compound suppliers that specialize in shipping milligram quantities to pharmaceutical research labs. You will use the eMolecules data management system to perform these tasks. You will have to interact with customers and suppliers by email or phone. You are a second or third year science major at one of the top San Diego universities available for 20+ hours per week. Work hours are flexible. Required skills: A solid knowledge of chemical structures, database searching and data management. Good online communication skills. Basic database and cheminformatics skills are a plus. Emolecules is the Amazon of Chemistry. We provide chemical search services for commercially available chemicals from suppliers worldwide. We provide custom eCommerce solutions for pharmaceutical and chemical research organizations. See www.emolecules.com ]]>

<![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a Documentation Assistant to work for a leading San Diego biotechnology company. Documentation Assistant The Documentation Assistant is expected to have a working knowledge of Good Laboratory Practices (GLP) as well as an understanding of the importance of document control. Responsibilities: * Responsible for following SOPs, as they pertain to document control and archival system. * Responsible for following GLP guidelines in the laboratory. * Assure compliance with GLP regulations and company procedures (SOPs and BPs). * Responsible for creating and archiving reagent logbooks. * Responsible for maintaining the document archives. This includes maintaining an index system and placing in the archive all raw data reports, protocol, and final report at study completion. * Responsible for updating SOPs, as changes are made to the archival system. * Assist with other QA functions as required. Please visit www.biophaseinc.com to view additional opportunities in San Diego County!]]>

<![CDATA[A qualified candidate must be familiar with ISO 13485:2003 and QSR; have hands on experience in document control, internal audit and external audit, CAPA, product release and non-conforming product handling, quality planning, organizing management review meeting, supplier qualification, data analysis. Prefer to have experience working in small IVD company, ideally IVD-reagent company. Interests or experience in regulatory affair is a plus. Other general requirements: · BS in Biology; · Lab work experience; · Excellent communication skills; · Excellent organization skills; · Must be able to multi-task · Excellent computer skills. · Detail oriented; · Must be a team player. · Must have project management skills ]]>

<![CDATA[You will process orders from research scientists in the life science industry and academic institutions worldwide. You will work with chemical suppliers, mostly screening compound suppliers that specialize in shipping milligram quantities to pharmaceutical research labs. You will use the eMolecules eCommerce system to perform these tasks. You will have to interact with customers and suppliers by email or phone. Required skills: A solid knowledge of chemical structures, database searching and data management. Previous chemical procurement experience is a must. Good online communication skills. Basic database and cheminformatics skills are a plus. Emolecules is the Amazon of Chemistry. We provide chemical search services for commercially available chemicals from suppliers worldwide. We provide custom eCommerce solutions for pharmaceutical and chemical research organizations. ]]>

<![CDATA[Duties: Employee will be required to work in large scale E. coli fermentation lab. Daily duties will include preparing sterile media and other sterile buffers, assisting in the inoculation, monitoring and harvest of fermentation vessels and light cleaning. Works in both a lab environment and manufacturing facility with specialized equipment. Employees may be required to operate automated and semi-automated equipment. The noise level in the work environment is usually moderate, lifting up to 20 lbs will be required on a frequent basis. May work in temperatures below zero degrees for short lengths of time. May intermittently sit at desk for a long periods of time to answer telephone and write or use a keyboard to communicate through written means. Skills: Job related tasks will require the use of basic lab equipment like scales, pH meters, incubators, UV spectrophotometer and centrifuges. Previous knowledge of this equipment is required. Previous experience in environment where sterile technique was used is also required. Prefer experience with E. coli fermentation but not required. Must be able to work with all Microsoft office programs and will need to learn Enterprise One data management system. Requires 0-2 years experience in the application of Microbiology laboratory techniques in a manufacturing environment or research laboratory. Demonstrated proficiency in the use of scientific laboratory techniques, equipment and materials required. Experience in the use of basic laboratory techniques, including buffer preparation, protein and nucleic acid gel electrophoresis, cloning, nucleic acid isolation and Western, Northern and Southern blotting is beneficial. Experience running E. coli fermentations up to 750L is desired. Demonstrated ability to carry out scientific procedures and make recommendations for improvement required. Good problem solving skills necessary. Working knowledge of manufacturing related computer software preferred. Education: BS Degree in life science with lab course work. Preferably microbiology or molecular biology. ]]>

<![CDATA[Well known research company seeks candidate to process daily requests for media and operate a variety of laboratory equipment required for media preparation. Must be able to use autoclaves, peristaltic pumps and analytical scales. Requires ability to adhere to strict aseptic processing guidelines during formulation of various reagents and cell culture media. Requires strict attention to detail. This is a contract position.]]>

<![CDATA[PROVEN Staffing has an immediate opening for a QA Associate with a biotech firm in San Diego. The QA Associate will be responsible for activities involving quality assurance and compliance to applicable regulatory requirements and ISO Standards, including: Review and analyze data and documentation as it pertains to customer complaints, failure investigations, corrective/preventive actions, internal and external audits, and internal training. Track, trend and report on quality system activities. Maintain a variety of metrics pertaining to quality system activities, including but not limited to corrective/preventive actions, training, audits. Participate in the development of slides for Management Review. Maintain the corrective and preventive action process, including tracking, trending and follow-up to ensure appropriate closure. This includes CARs, SCARs and ACARs. Provide assistance in other quality system areas as requested. Requirements: BS/BA degree in a scientific discipline. ASQ certification or equivalent training. Strong organizatonal skills. Strong oral and written communication skills. Strong interpersonal skills and ability to work as an effective team member. Minimum of 2 years experience in a FDA regulated Medical Device, Biotech or Pharmaceutical organization. Basic understanding of GMP requirements. ]]>

<![CDATA[Large Biotech Company in the Sorrento Valley area has an immediate need for a Production Chemist! *This is a full time, M-F, 7am to 3:30pm, temp to hire position* *The pay rate is $15-20/hour DOE* QUALIFICATIONS: * MUST have a B.S. degree in Chemistry. Only a BS in Chemistry will be considered* *Must have Manufacturing and Oligo experience* DUTIES: * Synthesize and purify scheduled quantities of DNA, AE labeled probes according to written manufacturing instructions and standard operating procedures to ensure that quality specifications and schedules are met. * Enters inventory and labor charges into the MRP system. * Assist in ensuring the department meets all applicable QSR and ISO 9001 regulations. * Develop and implement manufacturing documentation and standard operating procedures to ensure product uniformity, reproducibility and compliance with QSR regulations. * Maintain supplies of materials/reagents required to meet manufacturing schedules. * Alert supervisor of any material shortages, equipment requirements, or other circumstances which may cause delays in the planned manufacturing schedule. * Interface with OTS Oligo Dev personnel to learn production procedures for new products and to successfully oversee the transfer of knowledge and techniques to the Probe Manufacturing Department. * Maintain laboratories, working areas and equipment in a clean and functional state in order to comply with current federal QSRs. REQUIREMENTS: B.S. degree in Chemistry. Two years of directly related laboratory experience including DNA synthesis, HPLC purification, electrophoresis and solution preparation, preferably in a regulated environment. Good working knowledge of chemistry, biochemistry, laboratory and safety, mathematics, and federal QSRs. Demonstrable skills in verbal and written communications in English are required. Please email your resume today!]]>

<![CDATA[Research Technician Position (CB-Bottini): A research technician position is open in an academic laboratory at the La Jolla Institute for Allergy and Immunology (www.liai.org). The lab is focused on understanding how anomalies in T cell signal transduction play a role in autoimmune diseases and is currently developing novel therapies for autoimmune diabetes, rheumatoid arthritis, and systemic lupus erythematosus. Training will be provided in cell biology, immunology and signal transduction. Candidates must have a B.A./B.S. or higher in a biological science, chemistry, or biochemistry. Previous experience in a cellular/molecular biology laboratory is preferred. Please apply directly to: careers.liai.org/applicants/Central?quickFind=50359 ]]>

<![CDATA[The Veterans Medical Research Foundation (VMRF) is a private not-for-profit medical research corporation, providing support for biomedical and health services research. Qualifications Summary: Bachelor's degree (BA or BS) from four-year college or university; or two to three years related experience and/or training; or equivalent combination of education and experience. One to two years of experience in operation of electron microscopes required, in addition to experience in the operation of confocal microscopes. Knowledge of basic histology tissue preparation and sectioning required. The amount of experience will determine the level (I or II) employed at. Job Description Summary: Will coordinate physical preparation of laboratories and the scheduling of dates for experiments. Will coordinate the preparation and distribution for culture media, chemical solutions and other material. Will perform micro-technique procedures including knowledge of staining, and the ability to distinguish between treated and untreated tissue. Will prepare specimens such as paraffin, EM, hard tissue embedding and embedding frozen tissue in OCT compound. Will perform EM, hard tissue, paraffin and frozen (cryosectioning) tissue sectioning. Will operate a Zeiss 10 Transmission Electron Microscope and Gatan 785 Digital Imaging System. Will operate a Zeiss LSM 510 and Pascal confocal Microscope. Will operate a Zeiss Axio Observer, 21 Inverted Microscope with FRET, transmitted bright field, DTC and Epifluorescence capabilities. Will use established procedures to calibrate, control, and maintain a variety of instrumentation and laboratory equipment. Will use independent judgment in adjusting either the procedure or the mechanical device to bring procedures in line with good quality control standards. Will monitor inventory; requisition and order supplies. Will ensure that a sufficient supply of reagents, standards and controls are available at all times by ordering an adequate supply from commercial sources or preparing a variety of specialized solutions or reagents. Will answer phone promptly in a courteous manner, identifying self and service. Will handle outgoing calls appropriately and politely. Will show positive evidence of a helpful attitude to other staff, visitors and clients. Will promote attitudes and procedures that foster both internal and external customer satisfaction and ensures that staff is aware of organization customer service standards. Will maintain security of information in computerized systems in accordance with medical center policy, the Privacy Act, and other applicable laws, rules, regulations, and policies. Will perform general lab cleaning. Will inspect laboratory space for safe conditions and conformance to safety procedures. Will prepare core facilities invoices for jobs completed. May dissect, assemble and mount skeletal and other body parts. May prepare charts, graphs and/or models involving experimental data. May collect, classify and file scientific material. May perform other duties as required. AA/EOE. Please, no phone calls. To apply for this position, please use the following link: <a href="http://tbe.taleo.net/NA7/ats/careers/requisition.jsp?org=VETERANS_MEDICAL_RESEARCH_FOUN&cws=1&rid=160" rel="nofollow">http://tbe.taleo.net/NA7/ats/careers/requisition.jsp?org=VETERANS_MEDICAL_RESEARCH_FOUN&cws=1&rid=160</a>]]>

<![CDATA[A growing chemistry company in La Jolla, CA, is looking for a part-time Laboratory assistant. Job duties: • washing, drying, and re-stocking laboratory glass/plastic-ware generated by the lab. • monitor glassware needs and maintain stock. • maintain and cleaning of the glassware areas and certain portions of the lab. Requirements: • Ability to work independently under general supervision and follow written procedures with a high degree of accuracy. • Good verbal and written communication skills • Wear protective gloves, lab coats and safety glasses, as required. As a growing company, the candidate may be able to increase their responsibilities and hours in the future. We are looking for an entry-level candidate that wants to start a career in the chemistry industry with a growing company. The starting salary is $10 per hour. Interested candidates please submit your resume in your response. ]]>

<![CDATA[Research Scientist Assay Development – (Job ID 201002-130-05) Genomatica is seeking a Research Scientist Assay Development to join our growing enzymology team. This team is responsible for the identification and improvement of enzymes, including isolation, characterization and engineering of enzymes, for the cost-advantaged production of chemicals using microorganisms. This individual will be responsible for the screening and characterization of promising enzymes for the construction of metabolic pathways to produce chemical target compounds sustainably. This responsibility includes recombinant protein expression, purification and characterization of enzyme candidates, especially in regard to their kinetic properties, cofactor requirements and maximum conversion rates in to select the best enzyme for the production process. Also, the successful candidate will provide proof-of-concept studies evaluating various designed pathways to a given product and work in a team to establish metabolic strategies for the creation of high-performance organisms. This challenging position will require a motivated and organized individual with a Ph.D. in Biochemistry, Chemistry, Enzymology, Biology, or Microbiology and at least 4 years post-graduate and/or industrial experience in enzymology and/or assay development. The successful candidate will have a strong protein chemistry background, including enzyme mechanisms and a solid knowledge of metabolic pathways in bacteria/yeast. She or he will be proficient in recombinant protein expression (bacteria/yeast) as well as in a wide range of strategies to assess kinetic properties of various enzymes. Experience with the development of functional and quantitative enzyme assays suitable for high throughput screening is required. Familiarity with measuring enzyme activity on non-natural substrates, structure/function relationship analysis and the application of protein engineering to optimize enzyme performance will be beneficial for the role. Working within an interdisciplinary team will demand excellent communication and teamwork skills. Finally, this individual will be expected to be aligned and comfortable functioning within a rapidly growing company and a dynamic and spirited culture. Genomatica is committed to providing exciting career opportunities in a work environment that values trust, respect, openness, teamwork, creative talent, enthusiasm, and diligence. We are looking for innovative, motivated and uniquely talented people who enjoy the challenges and rewards of a burgeoning company devoted to commercializing cutting-edge technology. Genomatica offers a competitive compensation and benefits package. To inquire about this position at Genomatica, please send a CV or resume to hr@genomatica.com. To facilitate processing, please list the position Job ID 201002-130-05 in the subject line. Genomatica is an equal opportunity employer. ]]>

<![CDATA[Jonas and Associates Inc. is a growing environmental consulting firm with offices in northern and southern California. Our office in San Diego is seeking an Environmental Project Manager/Team leader to support our expanding services to public and private sector clients. Ideal candidate should have 15 plus years of professional remediation/technical experience. The candidate is required to have a degree in Geology, Environmental Science, Engineering (Environmental, Civil, Chemical, or Mechanical) or a related degree. P.E. or P.G. certification is preferred but not required. The candidate must demonstrate experience in the management of a technical multidisciplinary group. Candidate must have experience with Navy projects, and excellent technical writing skills, especially with the preparation and submittal of groundwater monitoring reports, remedial action plan reports, and closure request reports. Candidate will interact with the Navy Remedial Project Manager (RPM), trouble shoot problems, and work on business development. This individual should also have extensive experience in the development and mentorship of staff level employees. The candidate should have the ability to develop and implement short to long term business strategies and should have understanding of the local market and business opportunities. The successful candidate will be responsible for the oversight and management of staff personnel in performing subsurface soil and groundwater assessment investigations, management of environmental related field work, and ensuring regulatory issues are adhered to. Other responsibilities will include but not be limited to business development activities, including maintaining client relations, generating proposals, and provisional cost estimates. Jonas offers a competitive salary and benefits package. Jonas is an Affirmative Action Employer and strives for cultural diversity in the workplace. For immediate consideration, please send your resume to gmarkarian@jonasinc.com To learn more about JONAS, please visit www.jonasinc.com ]]>

<![CDATA[FAST PACED, GROWING BIOTECH COMPANY - IMMEDIATE OPENING! Our Senior Applications Specialist will work in tandem with our sales teams to manage and deliver high quality technical support. Our Senior Specialist will demonstrate, promote and install imaging and capital equipment for hospitals, health care, pharmaceutical and research markets. Our Digital Imaging Applications Specialist will identify customers, configure custom systems, manage pre-sales demonstration and coordinate the installations and training. 40% to 60% travel – with some possible International travel. REQUIREMENTS: 5 to 7 years experience with relevant technical and sales experience needed. Digital Pathology-Image Analysis Experience in a Medical or Clinical Setting Algorithms Processing Knowledge Understand image analysis tools and laboratory workflow Experience with Histology/Pathology applications Familiarity with CLIA, CAP and GLP guidelines a plus Solid organizational skills needed Trade Show participation EDUCATION: BS Degree in Biology or Engineering or related field MS or PhD Preferred COMPENSATION & BENEFITS: We offer a very attractive salary and a comprehensive benefits package including 401K and stock option plan. ]]>

<![CDATA[Client Coordinator / Liaison – office-based, not lab Prestigious firm seeks responsible professional with scientific background for office-based career as client coordinator / project manager. Involves liaising with clients and analysts in managing workflow on scientific and competitive intelligence consulting projects. Professional development opportunity within business-to-business environment for dedicated, career-minded individual looking for professional growth and success. Would suit someone with science background that wants to work in science, but outside of a lab. * Excellent communication and organization skills needed to handle multiple priorities and deadlines, with high level of focus and attention to detail. * Willingness and commitment to grow the business through building ongoing client relationships, coupled with business development and marketing to prospects * Unique career position suitable for responsible and professional person who is confident in dealing with high level business executives from science based corporations and intellectual property law firms Competitive salary/bonus and company benefits Requirements: * BS or higher degree in science, e.g. biology, chemistry, biotechnology, biochemistry, molecular biology, genetics, genomics, pharmaceuticals, etc. * Dedicated and reliable self-starter with sound decision making capabilities and excellent organization skills * Professional and positive attitude; personable and customer focused to work with customer needs and ensure client retention via managing expectations, trouble-shooting and problem solving * Knowledge of patent and scientific literature databases, intellectual property or patents in general is advantageous, but not essential. * Excellent written and verbal communication skills * Excellent computer skills * Works well independently as well as part of a team To apply for this position, please send resume and coverletter. ]]>

<![CDATA[Making Life Even Better. When it comes to the vision of shaping discovery and improving life, no other company can match the breadth of products and services in the life sciences field to meet this vision than Life Technologies. Created through the combination of biotechnology leaders Applied Biosystems and Invitrogen, Life Technologies’ systems, consumables and services enable researchers to accelerate scientific exploration, driving to discoveries and developments that improve the human condition and the world around us. Our customers do their work across the biological spectrum, working to advance personalized medicine, regenerative science, molecular diagnostics, agricultural and environmental research, and 21st century forensics. With historical sales of approximately $3.5 billion, a presence in more than 100 countries, and a rapidly growing intellectual property estate of over 3,600 patents and exclusive licenses, we are poised to truly shape the world of science. Join a team of more than 9,500 employees around the world who are engaged, curious, insightful, responsible and driven to make life even better. Life Technologies is looking for a Project Manager with extensive experience on medium and large projects. Candidate will be working with multiple teams, both on and off shore as well as project managers, business analysts and other stakeholders. This individual will be responsible for managing projects and reporting the status of projects on a weekly basis in accordance with the company’s PMO process. Essential Functions: Technical experience is a must, candidates need to have both management and technical programming experience. Specific functions include: − Define project scope, goals and deliverables that support business goals in collaboration with senior management and stakeholders. − Creates and executes project work plans and revises as appropriate to meet changing needs and requirements using PMO-defined tools. − Identifies resources needed and assigns individual responsibilities. − Manages day-to-day operational aspects of a project including scope and budget. − Reviews deliverables prepared by team. − Effectively applies our methodology and enforces project standards. − Minimizes our exposure and risk on project. − Ensures project documents are complete, current, and stored appropriately. − Coordinate the technical efforts of other IT groups and external vendors to ensure the effective development, modification, testing and implementation of systems to meet defined requirements. − Actively participate with customer groups in the planning for longer-term systems enhancements. May perform other related duties as required and/or assigned. Nature and Scope: This position interacts with all levels of internal customers and external vendors. That interaction requires excellent oral communication and customer service skills in identifying business needs and facilitating the implementation of technical solutions. Effectiveness in this role also requires thorough working knowledge of the customer’s operations, company systems and the ability to identify opportunities for new or improved systemization. The incumbent works on problems of diverse scope and moderate to high complexity where analysis of data requires a review of identifiable factors. Exercises judgment within generally defined procedures. The incumbent normally receives minimal instruction on routine work and general instruction on new assignments. Education: Bachelor’s degree in Engineering, Computer Science, Business Administration or a related discipline required. PMP certification is a plus. Experience: At least five years related experience or equivalent combination of education and experience. Thorough working knowledge of the standard project management practices, the company systems and available software packages required by the PMO processes. Proven problem solving, customer service and project management skills needed. Knowledge of Siebel CRM, Genesys and Unica is a plus Please apply to: www.lifetech.com/careers In the search area type in 3160 and apply]]>

<![CDATA[eBioscience (www.ebioscience.com) scientists have extensive expertise in antibody development, as well as personal histories of raising industry standards for antibody quality. Researchers worldwide have always been assured that their research funding and time are well-invested in eBioscience antibodies. Time and time again, eBioscience reagents have provided Researchers with the consistent, quality data that they expect. eBioscience reagents are utilized by leading laboratories worldwide. Since the company's inception in San Diego in 1999, our products have been widely cited in prestigious journals, including: • Blood • Immunity • Journal of Biological Chemistry • Journal of Experimental Medicine • Journal of Leukocyte Biology • Journal of Immunology • Journal of Virology • Nature • Nature Cell Biology • Nature Immunology • Nature Medicine • Proc. of National Academy of Science • Science Principle Accountabilities Research Associate II – Bioconjugation & Purification We are seeking a highly motivated Research Associate II, Bioconjugation & Purification, responsible primarily for the purification of antibodies and the development of fluorescently labeled bioconjugates. Essential Duties and Responsibilities include the following (other duties may be assigned.): • Carry out purification of monoclonal antibodies from hybridoma cultures • Carry out chemical modification/activation of fluorescent molecules, antibodies and recombinant proteins, bioconjugation and purification • Assist in carrying out product stability and formulation. • Assist in the transfer of process specifications and protocols to manufacturing • Follow cGMP protocols and procedures Job Dimensions • Carry out antibody purification • Carry out HPLC and SDS-PAGE analysis • Carry out and optimize appropriate methods for the conjugation, purification and characterization of bioconjugates and document all results • Enthusiastic and motivated collaborator with strong interpersonal communication skills • Significant skills in mainstream computer software are necessary. • Good communication (written and oral) skills and the ability to work in a multidisciplinary team environment are essential. • cGMP and ISO 13485 compliance Qualifications: • B.Sc or M.Sc. degree in Chemistry, Biochemistry, or Biology with minimum of 1yrs experience in the area of bioconjugations and biomolecule purification. Physical Demands and Work Environment: The physical demands and work environment described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to sit, stand, walk, talk and hear; use hands to finger, handle or feel; and reach with hands and arms. Benefits: We offer an exciting, entrepreneurial environment and a competitive compensation package, including salary, plus performance bonus and benefits (medical/dental and 401k). Plus, we work to maintain the best possible environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where each person feels encouraged to contribute to our processes, decisions, planning and culture. Our company culture is creative, fast-paced and entrepreneurial. We are a right sized environment where you can stand out and make a difference. EOE ]]>

<![CDATA[Summary -Senior Research Associate/ Associate Scientist need to work in a clinical oncology group. Perform validation of new clinical molecular assays using PCR, DNA sequencing and other modern molecular analysis techniques. Perform quality control activities including incoming reagent qualification, instrument performance verification, temperature monitoring, pipette calibration, etc. Strong background in molecular biology techniques (standard and real-time PCR, DNA sequencing, automated nucleic acid isolation, etc). This is a temp to hire on direct position ]]>

<![CDATA[We have an opening for a highly motivated individual with demonstrated abilities to design and execute rodent based ADME, PK, and toxicology studies. This position requires knowledge of drug metabolism and pharmacokinetic models and proficiencies in-life procedures. The primary responsibility of this position is to support the delivery of key ADME data to facilitate the goals of drug discovery and development projects through hands-on conduct of in vivo laboratory experiments. Seeking BS level candidate with 2+ years experience. ]]>

<![CDATA[Garcia and Associates (GANDA) is seeking a Project Manager to work from our Oceanside office in San Diego County, California. Specifically, we are looking for a prehistoric archaeologist with a minimum of a Master’s degree who has experience with the following: • Preparing proposals, managing and tracking budgets, and coordinating with staff, clients, and California tribes. • Solid field experience conducting and supervising all types of field projects (survey, excavations, and monitoring). • Prehistoric archaeology with at least 5 years of experience working in California. However, experience managing historical archaeological project is a plus. • A firm understanding of both state and federal cultural resources laws and regulations. • Experience coordinating with the California Office of Historic Preservation and other agencies. • Marketing and business development. The selected candidate will have superior writing skills and be capable of preparing Research Designs, Treatment Plans, Reports, and other documents. This is a full-time salaried position with benefits, commensurate with experience and qualifications. To apply, please submit your resume and a technical report sample to cdenardo@garciaandassociates.com. ]]>

<![CDATA[This position is to work as a production planner in Operations department in a fast growing biotech company. This job performs all functions needed to ensure product inventories are well stocked and maintained. 1. Monitor inventory levels in ERP/MRP to ensure that inventories are well stocked and all products are updated. 2. Plan and schedule production activities. Perform material transfers. 3. Responsible to work closely with production, QC, packaging and customer service groups to ensure that production schedules are met, and inventory are stocked without delay. 4. Responsible for inventory count and update. 5. Responsible for creating and managing product parts in MRP. 6. Assisting projects that would have special material stocking requirements and documentation. 7. Make requisitions for materials that related to inventory need. 8. Plan and schedule for new product development projects. Bachelor degree is minimum requirement. Knowledge in life science is a plus. Computer skills: MS Office especially EXCEL. Experience in MRP or ERP is desired. All interested candidates apply and submit resume online at www.biolegend.com ]]>

<![CDATA[Manager, QC Chemistry Grifols has been a leader in the healthcare industry since 1940 by creating innovative products and services based on the values of ethics, quality and responsibility. Grifols’ focus and mission is to fulfill the needs of its patients, as well as healthcare professionals working in therapeutics, pharmacy, diagnostics and blood banking. For more than 60 years, Grifols has developed, manufactured and marketed products designed to improve human health. At our Los Angeles facility, Grifols manufactures plasma derived biopharmaceutical products of proven efficacy, quality and safety. The Grifols family of companies includes Grifols Inc., Grifols USA, Grifols Biologicals, Biomat USA and Plasma Collection Center, Inc. Grifols Biologicals researches, develops and produces therapeutic proteins from human plasma and uses the most cutting-edge technology for protein purification. Our modern facilities are organized according to Good Manufacturing Practices (GMP) and have been certified under the FDA Establishment License. This division of our company has an immediate opening for a Manager of QC Chemistry, offering competitive salary, along with an excellent benefits package, including medical, dental, vision, 401(K) plan, life insurance, educational assistance, and five (5) weeks of paid time off. Job Responsibilities: (This job description is accurate at the date of publication and may change over time. It is not intended as an exhaustive description of the job. Other duties may be assigned and qualifications required may change.) Oversee the daily activities in the QC Chemistry laboratory to ensure that all cGMP, company specifications, procedures and guidelines are followed. Plan and analyze work flow, delegate and prioritize, to ensure tests and projects are completed in a timely manner. Direct the identification of assay problems and offer explanations and/or solutions where possible. Perform trending and investigations as needed and generate reports. Oversee the maintenance of accurate and complete records and review of test record results for accuracy and completeness. Provide hands-on guidance in the technical area of chemical laboratory operations when needed. Oversee and ensure adequate inventory of lab reagents and supplies. Conduct performance reviews of personnel. Write and revise laboratory standard procedures as needed. Assist in the development of, and performance of method validation studies and production validation studies. Designs and executes laboratory protocols necessary to complete Quality and Production-originated projects. Also, provides scientific advice and counsel regarding projects as needed Maintains current knowledge of regulatory and related scientific enhancements, trends and advancements through independent reading and training. Skills/Experience, Qualifications, and Educational Requirements: (To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions). MS or Ph.D. in chemistry, biochemistry or related scientific field. Minimum of 3 years of managerial or supervisory experience in a biologics, biotech, or pharmaceutical laboratory is required. Knowledge of and proficiency in the use of analytical instruments, including troubleshooting skills. Strong knowledge of small molecule analytical technologies (e.g. GC, HPLC, AA, etc.). Strong knowledge of analytical techniques for biologics or protein-based therapeutics. Understanding of immunological based method of analysis desired. Prior experience with blood coagulation products and coagulation-specific analytical techniques desired (APTT clotting assays, RCo and vWF analysis, etc.) Strong knowledge of cGMP regulations and prior experience successfully handling US and international regulatory agency audits and inspections. Ability to follow a wide array of Standard Operating Procedures and ensure laboratory personnel follow all SOPs. Experience with investigating Out of Specification events, and writing thorough reports regarding the investigational findings. Experience in statistical analysis and good computer skills. Excellent oral and written communication, as well as good organizational and decision making skills. Demonstrated leadership skills with ability to guide, train, coach and develop subordinates. Strong technical writing skills. Strong interpersonal and communication skills with ability to interact with all levels of personnel in a professional manner. APPLY VIA URL: <a href="http://hostedjobs.openhire.com/epostings/submit.cfm?fuseaction=app.dspjob&jobid=216875&company_id=16052&jobboardid=550" rel="nofollow">http://hostedjobs.openhire.com/epostings/submit.cfm?fuseaction=app.dspjob&jobid=216875&company_id=16052&jobboardid=550</a> Location: Los Angeles, CA 90032 Compensation: DOE Principals only. Recruiters, please don't contact this job poster. ]]>

<![CDATA[Dear Resarch Associates, One of San Diego's best biotech companies to work for is seeking a few Research Associates to join their team for 6+ months. Please submit your resume and references as a word document if you are interested in applying. Research Associate I Duration: ASAP-9/1/10 (may be extended) Pay: $15-17+/hr, DOE Job Description: -Duties will include preparing and operating amplified testing, both automated and manual. -Candidates will perform simple data analysis and notebooking. -Conducts basic laboratory bench experiments. -Participates in analysis and organization of data for presentation. -Writes experimental summaries and technical reports for own data. -Completes paperwork by assigned completion dates. -Carries out assigned laboratory tasks. -Monitor and maintain laboratory notebooks. -Operate lab equipment and perform routine maintenance/repair. Requirements: - BS in Molecular Biology, Microbiology, Biochemistry, Biology or related field and Minimum 1-2 years industry experience - Strong pipetting, PCR, molecular biology skills - Strong MS Word and Excel skills. ]]>

<![CDATA[Genoptix Medical Laboratory, Carlsbad, CA, is a rapidly growing, specialized CLIA-certified and CAP-accredited laboratory service provider focused on delivering personalized and comprehensive diagnostic services to community-based hematologists and oncologists. Currently, we have an open position in our Carlsbad, CA facility for a Lab Process Improvement Associate. Summary: The Lab Process Improvement Associate will assist in the development and management of continuous improvement processes for our clinical lab testing operations. They will also help to define and track appropriate metrics as measures of performance and success and provide creative solutions for improvements. Essential Duties and Responsibilities: Note: Other duties may be assigned. · Work closely with Lab Operations Manager to review operations, establish relevant performance metrics, suggest and help implement process and quality improvements, all within relevant regulatory guidelines. · Participation in implementation of new tests and lab equipment. · Assist with the interfacing between the IT Department and outside vendors to provide new and improved software/hardware tools for information transfer and data analysis. · Writing and supporting Excel-based data analysis and reports, along with QC software that is user-friendly and conforms to regulatory guidelines. Qualifications: · Desire and ability to work in and motivate interdisciplinary teams. · Demonstrated skills in project and resource management. · Basic computer programming skills or familiarity with good spreadsheet design and VBA macro-writing in MS Excel. · Familiarity with the concepts of process improvement and process engineering is a plus. · Excellent communication and interpersonal skills. Education and Experience: · Bachelor of science degree in a biological, chemical, Biochemistry, or bioengineering discipline. · Familiarity with basic statistical concepts and analysis. · A miminum of 4-5 years of related experience in a laboratory setting · Prefer experience in product development, quality, or regulatory setting in BioPharma or Clinical Diagnostics organization. Genoptix offers a competitive salary package with benefits including vacation and sick pay, extensive insurance coverage, flexible spending accounts, 401(k), employee stock purchase plan, tuition reimbursement and more. If interested, please apply via the following link: <a href="http://tbe.taleo.net/NA4/ats/careers/requisition.jsp?org=GENOPTIX&cws=1&rid=458" rel="nofollow">http://tbe.taleo.net/NA4/ats/careers/requisition.jsp?org=GENOPTIX&cws=1&rid=458</a> ]]>

<![CDATA[Great opportunity at leading San Diego biotech company! Perfect for Bioengineer grads with some industry experience! “The Power to Look Deeper” Awarded the 2008 Grand Prize at the local Workplace Excellence Awards, Gen-Probe is a respected biotech employer of choice in San Diego and a global leader in the research, development, manufacturing and marketing of nucleic acid probe-based products used for the diagnosis of human diseases and for screening of donated human blood. We offer a state-of-the-art facility in a prime location with world-class benefits. “The Power to Shape Your Future” We are seeking a mid-level Systems Engineer to be responsible for providing systems integration, reliability growth, and risk management in support of new product development for complex medical diagnostics instrumentation and improvement of existing commercialized products. DESCRIPTION OF POSITION RESPONSIBILITIES: •Conducts reliability or system tests to approved protocols. •Works with project sub-teams to plan and execute system testing. •Analyzes test data, manufacturing and field failures. •Conducts system level characterization notebook tests for product feasibility and development. •Conducts basic reliability and statistical analysis. •Works with cross-functional product development teams. •Assists with development of fault tree analysis, risk analysis, and failure modes and effects analysis (FMEA). •Works with external vendors to execute HALT and HASS protocols. RELATED BUSINESS/TECHNICAL SKILLS, KNOWLEDGE, ABILITIES: •Working knowledge of Windows applications •Knowledge of basic statistical and reliability analysis tools •Demonstrated ability to complete an engineering design or complex analysis under supervision. EDUCATION AND EXPERIENCE REQUIREMENTS: •BS/MS in Chemical Engineering, Bioengineering, or related field with 2-5 years of relevant systems, or related, engineering experience, preferably within the Medical Device, or closely related, industry. •Broad understanding of multiple engineering disciplines (e.g. electrical, mechanical, liquid handling, thermal analysis, software). Gen-Probe offers a dynamic and innovative work environment along with excellent benefits that include sponsored medical/dental/vision benefits, stock options (NASDAQ:GPRO), bonus potential, 401(k) w/company match, paid vacation/sick time /holidays, assistance with continuing education, on-site fitness center, and our own Waterfall Café. We invite you to view our Career Video! <a href="http://www.view-career-video.com/videos/genprobe/" rel="nofollow">http://www.view-career-video.com/videos/genprobe/</a> Please apply online by visiting: <a href="http://www.genprobe.com/careers/opportunities.aspx" rel="nofollow">http://www.genprobe.com/careers/opportunities.aspx</a> ]]>

<![CDATA[Genoptix, Inc. is a fast-growing, CLIA-certified, CAP-accredited clinical laboratory focused exclusively on the identification and management of high complexity hematolymphatic disorders. Currently, we have an open position in our Carlsbad, CA facility for a Clinical Lab QC Technician. Summary: We are seeking an experienced Clinical QC Technician to work within our Quality Assurance/Compliance department. This individual will perform quality control, calibration verification, and routine maintenance on various laboratory equipment. Essential Duties and Responsibilities: Note: Other duties may be assigned. · Perform quality control, calibration verification, and routine maintenance on various laboratory equipment. · Perform trouble-shooting and basic equipment repair as needed. · Maintain master equipment list and maintenance schedules · Organize and maintain equipment and QC records. · Communicate and schedule outside vendors as needed. · Work closely with laboratory supervisors and facilities personnel to assist with equipment-related issues. · Oversee Rees Centron Monitoring System. · Assist with Document Control activities as needed. · Assist with various filing as needed. Qualifications · Experience with laboratory equipment is required. · Requires good laboratory techniques. · Excellent organizational and documentation skills. · Excellent communication skills, both verbal and written. · Experience working with Microsoft Office, particularly Excel, to produce charts, graphs and spreadsheets. · Experience working with pipettes and microscopes is preferred. Education and/or Experience Bachelor’s degree in biology, biochemistry or molecular biology, or related science field, preferred. 1-2 years related experience in medical or scientific laboratory. We offer an attractive compensation package, including competitive salaries, comprehensive employee benefits & stock options. If interested, please apply online via the following link: <a href="http://tbe.taleo.net/NA4/ats/careers/requisition.jsp?org=GENOPTIX&cws=1&rid=444" rel="nofollow">http://tbe.taleo.net/NA4/ats/careers/requisition.jsp?org=GENOPTIX&cws=1&rid=444</a> ]]>

<![CDATA[BioLegend, a rapidly growing immunology research reagents company in San Diego, seeks an experienced Quality Assurance Supervisor. This position offers you the opportunity to make an immediate impact within a successful company. The Quality Assurance Supervisor will oversee all Quality Assurance (QA) activities at BioLegend, including oversight of manufacturing and quality control laboratory practices. Responsibilities include, but are not limited to: 1. Establish and maintain BioLegend’s Quality Management System (QMS). Oversee creation, review, and approval of all Standard Operating Procedures in the company, from raw material stage to shipping of finished products. Assure product, materials and process specifications are current and accurate. 2. Develop and implement methods and procedures for monitoring work activities, ensuring that products meet specifications and are produced and tested in compliance with approved procedures and applicable to appropriate state, federal, and international regulations. 3. Oversee training activities related to quality and reliability. 4. Provide corrective action and full resolution for non-recurrence to customer requests, customer feedback, inspections, audits, deviations and other related issues. 5. Conduct internal audits and investigations. Host, lead, and follow up supplier audits as necessary. 6. Manage the development and analysis of statistical data and specifications to determine present standards and establish proposed quality and reliability expectancy. 7. Work with internal department heads to ensure implementation of uniform quality practices and share/train best practices. 8. Provide ISO13485 training, as needed, to associates, and act as a resource to ensure quality compliance. Work with senior management to ensure that the principles of quality and compliance are inculcated into the company’s culture. Requirements: -BA/BS or equivalent experience in Biology or related field -2 years of experience in Quality Assurance under GMP, ISO9000, or ISO13485 regulations All qualified applicants must submit resume and apply on careers page of our website at www.biolegend.com ]]>

<![CDATA[The person in this position will be part of the Molecular and Cellular Biology group. The successful candidate will be supporting development of monoclonal antibodies. Essential functions include, but are not limited to: 1. General tissue, freezing banking and keeping records for different clones. 2. Culture and screening multiple hybridoma clones 3. Rodents immunization. 4. Rodent dissection 5. ELISA 6. FACS analysis Requirements: Bachelors of Science (or equivalent experience/education) in Biology, Molecular Biology, or related field. Standard tissue culture techniques, and general knowledge of hybridoma production. Knowledge of standard aseptic techniques, tissue culture, and ELISA, computer (Mircrosoft, Word, Excel, Powerpoint). In addition, the person should be motivated, flexible, and responsible. All qualified candidates must apply and submit resumes online on our Careers page at www.biolegend.com]]>

<![CDATA[MARINE BIOLOGISTS NEEDED FOR BEACH CLEAN UP DAY -- MARCH 27 Are you a marine biologist or have you studied marine biology? We are hosting three beach clean up events on March 27, and we need instructors for the kids. The kids will spend a few hours cleaning up the beaches, then you will give a short presentation on why beach cleaning is important to the ocean. Does this sounds like something you would be interested in? If so, please respond to this email with your name, phone number and relevant experience. THANK YOU!!!]]>

<![CDATA[Operations Department of a growing, international biotech company is searching for a qualified, experienced scientist to help lead others in the path to legendary discovery. Major Duties and Responsibilities (including supervising others): • Independently, design and execute experiments for process development, optimization, scale-up, technology transfer, and validation. • Effectively troubleshoot and provide technical services for manufacturing processes. • Carry out, input technical direction and execute custom projects. • Influences the course of projects, scientific methods and/or company's technical direction • Proactively identifies complex obstacles to progress; recommends and implements solutions using a diverse set of resources; solves problems in creative and effective ways; challenges current processes and recommends novel approaches • Mentors Research Associates and lower level Scientists Qualifications: • Ph.D. in life science with thesis, publication(s) and minimum two years of relevant experience • Possess high level protein chemistry skills, including purification, labeling and fragmentation, with demonstrated application and creativity • Demonstrated ability to successfully direct and execute multiple projects simultaneously and ability to meet project deadlines • Excellent communication and ability to work in a team setting Physical demands: • May exposure to hazardous/toxic/dangerous chemicals • Handle basic lab equipments Travel Requirements: • May travel to attend scientific conferences, <10% All qualified candidates must apply and submit resume online on the Careers page of our website: www.biolegend.com ]]>

<![CDATA[This position demands a motivated, patient, business-minded individual with the extensive background and experience of a scientist. If you are ready for the challenge a fast-paced, growing, international biotech company, then you must apply! The Technical Service Scientist will provide technical solutions to external and internal customers. Duties include, but are not limited to: responding to technical related emails and phone calls from customers, distributors, and sales reps; technical writing of marketing literature; website content editing; participating in business development, marketing, and sales activities; attending tradeshows; and generating new leads. Candidates should have: -Minimum MS/BS in Biology related field + 3 years lab experience or recent PhD -Hands on experience with flow cytometry (instrumentation & software) preferred -Familiarity with ELISA, western blot, IHC, Luminex platforms are a plus -Excellent oral, written, and electronic communication skills in a professional setting -Ability to be flexible, time manage, and multitask All interested candidates need to submit resumes and apply on the Careers page on our website: www.biolegend.com ]]>

<![CDATA[Clinical Research Coordinator Profil Institute for Clinical Research, Inc. (“Profil”),is a private research institute based in Chula Vista, California. At Profil we are focused on early-phase clinical investigations (Phase I and II) of potential new treatments for Diabetes and other metabolic diseases. <a href="http://profil-research.com" rel="nofollow">http://profil-research.com</a>. • We are currently seeking a Clinical Research Coordinator who is highly motivated and will enjoy contributing to high-quality research. The ideal candidate will Participate in and manage all administrative aspects of clinical trials within Profil Institute for Clinical Research (PICR) under the direction and supervision of Senior Clinical Project Manager. Specific Responsibilities: Clinical Trials: • Review of client protocols and case report forms for all study related logistical issues. •Establish and maintain up-to-date study specific regulatory binders and files. •Coordinates and manages regulatory documents and all IRB interface. •Reviews / creates study specific source documents and, if required also study case report forms •Initiates and keeps track of study specific volunteer recruitment activities. •Prepares study specific schedule outlining all volunteer visits, keeps track of all study specific volunteer visits •Plans for all study specific staff requirements concerning clinical operations staff. •Explains IRB approved subject informed consent forms and obtains subject signatures under confidentiality requirements. Instructs subjects on treatment methods and protocol. •Supports nursing staff in day-to-day clinical activities and procedures, ensuring efficient workflow and adequate care and treatment of research volunteers. •Supports nursing staff in administering prescribed study medications, performs phlebotomy, monitors vital signs and/or performs other specialized procedures, as appropriate to the specific needs of the study and individual subjects. •Supports nursing staff in monitoring and recording subject response to treatment, questioning subjects on adverse events/serious adverse events during study, completing study specific subject information on Serious Event Forms. •Lab support including kit preparation, specimen preparation and specimen shipping. •Works with nursing staff to resolve study source document discrepancies •Completion of study Case Report Forms. Clients: •Main operational interface with study sponsors when a study is in planning stage and during study implementation. •Main IRB Interface Training: •Responsible to train all staff on specific protocol related items as needed Requirements Education Requirements / Certifications: •Medical Assistant, LVN or LPN, Registered Nurse or Bachelors •Participation in PICR training program Skills / Experience: •Previous clinical research experience preferred •Knowledge of Good Clinical Practice (GCP) as it applies to clinical trials •Leadership and people skills •Ability to work independently •Initiative, problem solving At Profil, we offer a competitive and comprehensive salary and benefits package. If interested, please submit your resume to: hrpicr@profil-research.com ]]>

<![CDATA[Manufacturing Process Technician needed for large Biotech company! Duration: Start immediately and set to last through Aug 2010. This may be extended. Shift: 6:30am-3pm, M-F Pay: Level I: $12 to $16/hour depending on experience *Must have filling experience! Description of duties to be performed: * Understands and executes written procedures. * Operates basic Packaging and/or Filling equipment. * Applies labels according to SOP’s. * Maintains detailed and accurate device history records Stocks laboratory with supplies. * Cleans laboratory Cleans Labware and equipment. Qualifications Please send your resume today!]]>

<![CDATA[Aubrey Inc. (www.AubreyInc.com) is a new bioengineered wound dressing manufacturer that is looking for a Director of Regulatory Affairs/Quality Assurance. Our Ideal candidate must have superior time management abilities, great attention to detail and the ability to multi-task in a fast-paced environment. Position Summary: Assure that the company has effective systems and programs which result in compliance with all applicable medical device regulations and standards. Determine organizational objectives and Quality System updates required to both support and promote continued aggressive growth in a compliant and cost-effective manner. Duties and Responsibilities: • Responsible for regulatory compliance with: FDA, ISO, CMDR, Notified Bodies, and foreign regulations. • Serves as the Quality and Regulatory authority to the company as required. • Responsible for interactions and negotiations with applicable regulating agencies and business partners regarding product compliance, both domestically and internationally. • Responsible for the creation and maintenance of regulatory submissions within and outside of the United States. • Management Representative responsible for implementing and maintaining a compliant Quality System per FDA and ISO requirements; represents company during medical device regulatory agency audits and inspections. • Responsible for assuring compliance of products manufactured. • Assuring quality system requirements are met and distribution requirements are maintained to meet corporate business goals and objectives. • Promote organization's growth and adherence to industry standards in regard to product assurance, validations, design controls, document and data controls, supplier management, statistical techniques, etc. This includes overseeing the technical review and approval of individual scientific and engineering protocols and reports as well as the identification of next-generation Quality System methods and toolsets. • Oversee the Quality Assurance function with the independence and authority to ensure quality processes and products. • Oversee internal quality system audits, supplier quality audits, due diligent audits. • Responsible for department budget and adherence to business plan, goals and objectives. • Provide support with compliance and quality assurance decisions as needed to: QA, Operations, R&D, Sales and Marketing, Clinical Affairs and Executive Management. • Responsible for corporate deliverables, as required. Qualifications: • Bachelor’s degree from a four-year, accredited college or University. Bachelors of Science in Engineering or Life Science. • Fifteen years experience in a medical device or biotechnology company in the capacity of Regulatory and/or Quality Assurance function. • Knowledge and direct working experience with ISO 13485, FDA GMP’s, MDD and CMDR regulations. • Experience working and negotiating with regulatory agencies serving as the company liaison. • Experienced directing activities for obtaining PMA, 510K and CE mark approvals. • Good teamwork and interpersonal skills, good communication and presentation skills, English communication skills Application Process: • Email a cover letter including salary requirements and your résumé to info@aubreyinc.com. Candidates that do not include salary requirements will not be considered. ]]>

<![CDATA[IMMEDIATE PRODUCT MANAGER OPENING APPLY NOW.... Great Company .... Fantastic place to work.... PRODUCT MANAGER BIOTECHNOLOGY (PD-1-7729) We are looking for a Product Manager with a strong track record of product implementations. Our Product Manager will develop, define and manage our product strategy. The Product Manager will manage all aspects of our Product Portfolio to ensure sales targets, market share, and profits. We are looking for a high velocity Product Manager who can work in a fast pace environment with a talented engineering, marketing and sales teams ! PRIMARY DUTIES Manage our product line life cycle from strategic planning to tactical activities Specifying market requirements for current and future products by conducting market research. Drive a solution set across development teams (primarily Development/Engineering, and Marketing Communications) through market requirements, product contract, and positioning Developed and implementing a company-wide go-to-market plan, working with all departments to execute Analyzed potential partner relationships Strong understanding of Business User and Consumer web portal methodologies Analyze product portfolio sales trends and pricing to identify areas for improvement or strategic focus. Develop and implement an agreed marketing plan for the portfolio working alongside the Product Marketing team. This involves implementation of positioning, channel, pricing and sales support, advertising and promotion Utilize market information, voice of the customer and Research & Development to identify new product opportunities Work closely within the product development team to manage products through the new product development process to deliver a successful launch Coordinate with commercial teams to deliver timely and effective product launches, including providing training materials for internal technical service and sales teams and effective forecasting Responsible for web content and catalogue content Work with Sales Specialists and Regional Product Managers to set list pricing and discounting policies for both direct and distributor channels Work with Operations to ensure that agreed service levels are in place for timely customer delivery of specific products Analyze viability of requests for customized products/OEMs, and launch where appropriate Recommend and implement approved discontinuation strategies Provide pro-active communication with senior management regarding the product portfolio, its performance and any major issues or changes in the market or competition QUALIFICATIONS : Computer literacy, particularly with Microsoft Word, Excel and PowerPoint Excellent technical written and oral communication skills Pro-active problem solver Self-managing and self-motivating individual who can prioritize tasks effectively and meet customer expectations and deadlines REQUIREMENTS:: 7 years of relevant professional experience in product management and marketing 7 years of direct product management in either a distribution or manufacturing company Master’s degree in science or an MBA + a bachelor’s degree in a life sciences discipline (i.e., biochemistry, molecular biology, immunology or physiology) Experience creating PowerPoint slides and presenting to large and diverse audiences Able to travel internationally up to 20% of the time, possibly on weekends and over holidays Computer literacy, particularly with Microsoft Word, Excel and PowerPoint Excellent technical written and oral communication skills BENEFITS To attract and retain the best professionals, we offer an exceptional salary and an extremly competitive benefits package. Please forward your resume and salary details with job code (PD-1-7729) . Previous experience in Biotech ,High Technology or the Medical Industry ]]>

<![CDATA[Laboratory Research Technician Needed for Part-time, temporary position, up to 20+ hours per week in Rancho Bernardo, CA. Qualifications: BS Candidates with lab experience in Protein Biochemistry, Enzmology, or Immunochemsitry Competitive Salary Offered Please send all resumes to vtshumanresources@gmail.com ]]>

<![CDATA[Primarily responsible for input online, phone, and fax orders and relative data into the ERP system. Responsible for responding and investigating to all customer inquiries regarding shipments, products and complaints. Responsible for answering incoming phone calls. Essential Functions: 1. Responsible for processing fax/email orders/phone orders 2. Main job focus will be to complete fax/email orders, and serve as a backup for our phone reps answering calls when necessary 3. Receive, investigate, and respond to all customer inquiries regarding shipments, products, and complaints 4. Process customer orders and revisions according to established company policies and procedures 5. Process customer returns according to established company policies and procedures 6. Follow up with customers when necessary to advise shipping delay and/or obtain additional information to process orders 7. Maintain composure and professionalism when handling irate customers 8. Cross train on other departmental duties to expand knowledge and skill set 9. Correspond with customers to solve any problems that may arise 10. Perform delivery checks on shipments when requested 11. Provide accurate information to customers regarding order status and product availability 12. Help facilitate marketing strategies that are implemented 13. Send out correspondence when necessary 14. Complete projects as assigned 15. Troubleshoot customer orders Skills and Qualifications: -BS degree in Biology or related field or Equivalent work experience in a Biotech company -Customer Service and/or Administrative experience required. -Must be detail oriented and have a high level of accuracy. -Must be able to follow instructions, and work within a team atmosphere meeting daily deadlines. -Must have the ability to multi-task and time manage multiple priorities and speak clearly and concisely in a professional manner. All interested applicants must apply and submit resume online on the Careers page of our website: www.biolegend.com ]]>

<![CDATA[At ACON Labs, we are making a difference in medical care by offering rapid tests and medical devices for diagnosing a variety of conditions. In addition, we are able to streamline and reduce costs for the physician and/or patient directly. Come join us in developing the latest technologies that enhance human life and be a part of our growing, dynamic company. We are looking for a self-motivated individual to help plan, organize and control assigned existing and/or new product(s) from conceptual stage through product life cycles to optimize profile and meet marketing, financial and corporate growth objectives thru product market research, development and launch. The ideal candidate would also be hardworking, detail oriented, and a quick learner. Responsibilities: • Participate in overall product market research, design recommendations and definitions, product development and launch, and manufacturing coordination for assigned existing and/or new product(s). • Assist with product packaging and labeling/artwork process (creation, revision, and/or customization) for any/all products within business segment and effectively communicates/collaborates with packaging and labeling staff and CSS for order entry/new artwork implementation. • Interface with clients/support teams for new product development projects and packaging. • Assist with product launch & refresher training & support material to colleagues/customers in support of products in business segment. • Coordinate product promotional activities: press releases, advertisements, sales tools (e.g., sell sheets), website visibility. • Collaborate with team representatives to conduct continuous product/market trend surveillance, produce competitive analysis materials comparing product with its key competitors, and study product complaint trends to assist in product improvement. • Establish and maintain a positive and effective two-way communication of product concerns and needs with other departments. • Assist with new products requests and other business endeavors as assigned. Requirements: • Bachelor’s degree in Bioengineering, Biology, Immunology or related discipline; or combination of education and directly related experience • Technical/scientific background experience and/or education • 1-2 yrs experience in R&D, technical troubleshooting in IVD industry • Must have excellent verbal, written and phone communication skills • Proficient in Microsoft Office (WORD, PowerPoint, and Excel) • Mandarin fluency, preferred This position is located in our corporate office in San Diego’s biotech community. As an ACON Labs team member you’ll enjoy our competitive benefits and compensation packages, as well as working in a supportive team environment. We invite you to consider a career with ACON Labs by sending your resume to hr@aconlabs.com. Please reference job code IM014. ]]>

<![CDATA[This position entials the design and performance of assays for a wide variety of targets (enzymes, receptors and functional cell-based assays with fluorescence, FP, TRF and reporter gene readouts. Assays will be implemented robotics and the candidate will safely calibrate, program, optimize methods and operate automated liquid handling and analytical equipment. Must be able to follow and write laboratory protocols to ensure reproducible results, accurately record results of experiments, calculate results and prepare summaries. Requirements: A Bachelors degree in a relevant scientific discipline, and at least 7 years experience with molecular and cellular biology methods as applied to assay development and screening. Experience with use, calibration and maintenance of laboratory automation in support of lead optimization and assay development is required. Demonstrated expertise with the recording, calculation and graphing of experimental results from complex experiments using Excel and Graph Pad Prizm or equivalent software is required. The individual should be able to work independently, have very strong laboratory and problem solving abilities, and excellent record keeping and communication skills. Three years experience with calibrating, programming, optimizing methods and operating automated liquid handling equipment Three years experience with the of assay development for a wide variety of targets (enzymes, receptors and functional cell-based assays with fluorescence, FP, TRF and reporter gene readouts. Experience working in a high throughput drug discovery environment. ]]>

<![CDATA[Genomatica is a sustainable chemical company that commercializes novel bio-manufacturing processes to produce a variety of industrial chemicals that impact all major industries and provide the materials that comprise the world we live in. The Company enables the production of sustainable chemicals through a compelling proprietary Integrated BioProcess Engineering Platform. Our unique capabilities fundamentally transform the way in which Nature can be leveraged to convert low cost feedstocks into high-value chemicals. These sustainable chemical products will benefit the world by reducing dependence on hydrocarbon feedstocks and improving the environment via safe, clean manufacturing processes. Genomatica is seeking a highly motivated Research Associate Microbiology to join the growing microbiology/fermentation and evolution team. This team is responsible for construction, characterization, evolution and fermentation of hosts strains. The successful candidate will utilize her/his knowledge of molecular biology and microbiology to screen and select the best hosts for Genomatica’s production processes. Responsibilities: • Construct and isolate hosts strains (bacteria, yeast) using various cloning techniques • Cultivate at small (96 well plates) and medium scale candidate strains • Develop HTP cultivation techniques for screening processes • Evolve and characterize strains (growth, metabolite profiling…) • Work and interact on a daily schedule with the molecular biology and fermentation teams • Acquisition, evaluation, and presentation of data • Follow and create standard operating procedures • Operation of proprietary devices for microbial evolution Qualifications: • BS in microbiology or molecular biology • Experience in isolation, culture, storage and archiving of various microorganisms • Excellent laboratory skills, proficient in a wide variety of molecular biology techniques (DNA cloning, recombination, DNA isolation…) • Experience with high throughput cultivation techniques • Basic understanding of fermentation (Small scale) is helpful • Experience and understanding of evolution preferred • Very good computer skills, able to manage, organize, and critically evaluate data • Excellent organization and communication skills (both written and oral) absolutely required • Must be self motivated and detail oriented • Able to adjust and thrive in a fast paced, dynamic, team driven work environment ]]>