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<![CDATA[DATA ENTRY WITH A TWIST! Do you like working as part of team? Do you enjoy a job that is multifaceted? Are you ready for the challenge of a Data Entry position with a twist? These are the qualities we are seeking: Unwavering dedication Responsibility and accountability Integrity in character Noteworthy attitude Energetic with an Eye to detail Rapidly growing drug screening laboratory is currently seeking to add more Information Processing professionals to their already dynamic group of individuals. We are seeking only positive, friendly-upbeat individuals that are driven to be the most accurate, detailed driven individuals that can and will be an asset to our company for years to come. This is not your ordinary data entry job or company. It is imperative that information is entered into our data base not only 100% accurately, but you must also possess a high typing speed. To find a candidate that can prove both requirements in this position has been challenging. This job is a little more challenging than a normal Data Entry or Information Processing position but it is worth the challenge. If you feel you have the all capabilities; are ready for a new challenge and are able to be flexible with company changes; please read additional qualifications. Speed and accuracy will be measured and monitored continuously! Qualification/Requirements: • High school diploma or GED • Type 60 WPM with high accuracy (test will be administered) • Medical and/or billing background and/or transcriptionist is a plus • The ability to be at a computer for 80% of your day performing rapid/accurate data entry of medical testing and patient information • The ability to meet expected goals of entering 100+ requisitions daily with complete accuracy on test entered and patient/practice information • Able to contribute and be an asset to the company while leaving all drama out of the office • Willing to set goals and strive to be the best team player with current staff • Able to work overtime when necessary If you feel you are capable and meet all above listed qualifications, please send your RESUME, COVER LETTER, and SALARY HISTORY immediately. Please note that only applicants who meet the above listed requirements and follow all directions will be considered. All applicants interested in interviewing for this position must not ]]>

<![CDATA[The Wildlife Research Institute, located in Ramona, CA, is recruiting Interns for biological monitoring and other work. These Interns will assist in a variety of field and computer-based biological work. Both part- and full-time, paid and volunteer, positions are available. Interns will have an opportunity to learn about natural resources, get fieldwork experience, network with other biologists, and learn about this kind of environmental work. Some positions require spending extended periods in the field, often under rigorous conditions. Interested parties should contact Dr. Jeff Lincer, Research Director; (619) 337-4060 and email resumes to JeffLincer@gmail.com.]]>

<![CDATA[Sapphire Energy is a venture capital backed company developing next generation biofuels based on recent advances in metabolic engineering. The company focus is the commercialization of high performance, low cost, and low carbon footprint biofuels that will substitute for conventional gasoline, diesel, and jet fuel. We are seeking an energetic, results-oriented Temporary Research Associate to join our Analytical Chemistry group. The role requires you to provide laboratory based routine support to the Analytical Chemistry team. Within this role you will be required to perform a variety of routine research/laboratory tasks and experiments under general supervision, collect and tabulate results. The selected individual will have a solid understanding of sample preparation and wet chemistry-analytical lab techniques and ability to function in a highly collaborative, cross-disciplinary environment, and will provide routine support activities as they relate to the functionality of lipids in algae biofuel production processes and technologies. Responsibilities: •Thorough knowledge of laboratory techniques with an emphasis on performing sample preparation techniques like extraction, derivatizations or related experiments •Accurate and reproducible execution of standard analytical techniques and record data. •Ability to effectively communicate results and interacting with project team scientists and engineers, as well as external collaboration partners. Ability to work effectively in a team environment. •Ability to provide service in a courteous, prompt, and efficient manner. Ability to establish and maintain strong working relationships with colleagues. Ability to get along with diverse personalities. •Ability to express oneself clearly and effectively in written and oral form and request clarification when needed. Requirements: •Bachelor’s degree in Chemistry or Biochemistry with a minimum of 2 years of experience – laboratory prep experience in an industrial environment is preferred. •Must be able to participate in highly effective teams. •Requires ability to use common tools for effective scientific communication within the company. •Demonstrates ability to recognize and report anomalous and inconsistent observations/results. To apply, please send your CV and salary requirements to human.resources@sapphireenergy.com and reference “Temporary Analytical RA” in the subject line. ]]>

<![CDATA[Genomatica is a 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’s Molecular Biology group is seeking an experienced, highly motivated Research Associate II to work with cutting edge Molecular Biology technologies to develop renewable chemicals. The successful candidate will join and support an interdisciplinary group of biologists dedicated to designing, discovering and optimizing novel of biochemical pathways. The group is involved in a milestone driven, proof of concept project with a goal of validating target genes that will ultimately convert renewable feedstocks into commodity chemicals. Strong technical, creative, organizational and communication skills are essential. Responsibilities: • Conducting molecular biology experiments, including molecular cloning (DNA isolation, PCR, DNA mutagenesis, RT-PCR and Protein analysis) • Performing small scale experiments to test pathway enzyme activities (including enzymatic assays) • Continuous documentation, analysis and interpretation of experiments in the form of laboratory notebooks as well as timely entry of information into a LIMS database. • Presentation of analyzed and summarized results in both written and oral format and delivery of completed reports. • Work independently as well as collaboratively with other team members to accomplish project goals and milestones. Qualifications: • Degree in bioengineering, molecular biology, biochemistry, or equivalent • BS/BA and 2+ years experience or MS degree, preferably in the biotechnology or pharmaceutical industry • Broad molecular biology expertise, and data management • Lab management experience desirable 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 facilitate processing, please list the position Job ID in the subject line. Genomatica is an equal opportunity employer. No relocation is provided for this position. ]]>

<![CDATA[Genomatica is a 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 to join the growing Enzymology and Protein Engineering 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. Responsibilities: • Evaluate expression, solubility and activity of recombinant proteins • Perform enzyme activity assays • Characterize enzyme candidates • Perform high throughput screening of large protein libraries • Acquisition, evaluation, and presentation of data and results • Follow standard operating procedures • Growth of host cells (bacteria and yeast), protein detection and purification Qualifications: • BS in biochemistry, molecular biology, or microbiology • A minimum of 2 years relevant experience working with enzymes or proteins • Excellent laboratory skills with proficiency in a wide variety of biochemistry techniques (bacterial/ yeast culturing, protein production, purification and analysis, enzyme assays) • Very good computer skills, able to manage, organize, and critically evaluate data • Excellent organization and communication skills (both written and oral) required • Must be self motivated and detail oriented • Able to adjust and thrive in a fast paced, dynamic, team driven work environment 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 facilitate processing, please list the position Job ID in the subject line. Genomatica is an equal opportunity employer. No relocation is provided for this position. ]]>

<![CDATA[--------- CHEMIST-LAB TECHNICIAN Full time & Part time. We are looking for Full Time and/or Part Time LAB TECHNICIANS for polymer chemistry production. REQUIREMENTS: 2+ yr lab experience, related work experience preferred. 2 years laboratory classes may be considered. Bachelors degree preferred. Experience demonstrating good documentation and record keeping skills. DUTIES: Applicant must follow standard operating procedures (SOPs), perform product quality control possibly with spectrophotometer, microscope, viscometer. Must conduct routine cleaning of lab, glassware + equipment, and solvent preparation. Attention to detail, good communication, and accuracy are essential. Ability to multi-task and assist others with workload. Ability to maintain accurate documentation and organize records. Must work well with others in a team environment. Ability to troubleshoot. Salary or hourly rate depends on experience. Range 12-17$/hr. Work hours for full time, approximately 8am – 4:30pm. Benefits for full time positions. Work hours for part time, variable within shift 8-4:30. Please fax or email: ----A Cover Letter AND a Resume. ----Specify on cover letter which position you are applying (Full Time or Part Time). ----If applying for a part-time position please specify the days, times, and total number of hours you are available for work. Fax: 858-677-0212]]>

<![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a Scientist to work for a leading San Diego biotechnology company. Scientist, Diabetes Our client is seeking a skilled Scientist to work with the Diabetes Care team to design and conduct research and development studies. This person will investigate, create and develop new methods and technologies for project advancement, analyze data and propose strategic direction. In addition, the person may lead a team of one or more scientist(s), research associate(s) and/or research technician(s) for daily project activities. Requirements: * Bachelor’s degree in chemistry, biochemistry, or a related field with up to 5 years of experience in assay development and improvement process in a quality system environment. * IVD industry experience in electrochemical biosensor development. * Excellent oral and written communication skills, including proven ability to write scientific and technical reports. * Excellent problem solving and analytical approach are required. * Requires knowledge of computer programs including data analyses and graphing software programs. * Experience in optical biochemistry assay development, preferred. Visit <a href="http://www.biophaseinc.com" rel="nofollow">http://www.biophaseinc.com</a> to view our current job postings!]]>

<![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a Histologist to work for a leading San Diego biotechnology company. Histologist Duties/Responsibilities: * Performing technical and scientific processes and procedures in the Histopathology section of the CLIA laboratory, including pre-analytical, analytical and post-analytical duties. * Operating, maintaining and calibrating instrumentation utilized in the testing process (Autostainer, Digital Imaging, Microtome). * Evaluating test results for completeness, accuracy and quality prior to slide review and interpretation by the Anatomic Pathologist. * Ensuring quality control and quality assurance protocols and procedures are followed, as established. * Ensuring safety protocols are followed, as established. Assisting in the creation and implementation of laboratory documents (ie: Training documents, Standard Operating Procedures). * Preparing reagents, as needed. * Ensuring proper inventories of consumables and reagents. * Assisting in R and D, as directed by scientific team. * Performing duties as defined as Category I: Tasks or procedures that involve exposure to HIV, HBV, HCV, or any other infectious material, including working with blood, body fluids or tissue. * Monthly pH check on glassware * Quarterly eye wash station checks Education/Experience: * Required to hold a Bachelors of Science degree in Life Sciences. * Required to hold an active HT (ASCP) license * Required to have a minimum of 3 years in a CLIA certified, high complexity laboratory performing Histology. * Preferred to have Certification in Immunohistochemistry (QIHC) Visit <a href="http://www.biophaseinc.com" rel="nofollow">http://www.biophaseinc.com</a> to view our current opportunities!]]>

<![CDATA[Leading biotech company in Mira Mesa has an immediate opening for an experienced Packaging Technician. The successful candidate will have 1+ years recent experience packaging at a biotech or life sciences company. This position will subdivide, label and package biochemicals using defined procedures. This includes, weighing powder and liquid material, utilizing electronic balances/scales and pipettes. Fills appropriate containers with correct quantity and seals, labels and packages final product. Materials required may include solvents, measuring equipment, safety clothing equipment, bulk powder and liquids. Experience with SAP or an ERP system is preferred, along with experience in writing or revising SOPs and work instructions. Must be able to stand for extended periods and lift or move up to 50 pounds unassisted. Must have experience using: -the metric system sufficient to perform basic math calculations. -the use of electronic scales, including analytical and micro-balances, pipettes, graduated cylinders. -and strong experience in the use of computer and MS Office applications. Basic knowledge of ISO9000 and/or Good Manufacturing Practices (GMP) Hours are M-F 6am -2:30 pm. Qualified candidates please submit your resume via e-mail for immediate consideration. ]]>

<![CDATA[A biotech company in Torrey Pines seeks a QA Associate II. Qualified candidate must have 2 to 3 recent years of quality assurance experience in a biotechnology related manufacturing environment. Must possess detailed knowledge of ISO and GMP standards. Working knowledge of SAP is preferred. Will be responsible for planning, executing and following-up internal and external audits, create and revise QA SOPs; review and approve Operations' SOPs, prepare and present Quality training/education seminars for company personnel. This is approximately a 3month assignment to start immediately. Hours are 8-5pm.]]>

<![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 Research Associate II We are seeking a highly motivated Research Associate II scientist to join the R&D team to develop, test, and validate novel reagents. The candidate will be responsible for working closely with the scientists in product development from inception to release. The candidate must be able to work effectively in a collegial fast-paced environment and have excellent communication skills. This is a great opportunity for a dynamic goal-oriented scientist to utilize their expertise and contribute to a rapidly growing company. Essential Duties and Responsibilities include the following (other duties may be assigned.): ? Perform antibody-based immunological techniques, including flow cytometry and western blotting. ? Maintain primary cell cultures and cell lines. ? Communicate project status and test results to the R&D team regularly. ? Maintain detailed and organized documentation. ? Work as a team with other R&D staff members to contribute to the release of novel, high-quality reagents. Qualifications: ? BA/BS in Biology, Immunology or related science. Thorough knowledge in immunology, cancer biology, cell biology, or other related field ? Should have 2-5 years lab experience in immunological techniques, specifically flow cytometry data analysis on different platforms/software ? Should be able to design, conduct, and troubleshoot experiments independently ? Excellent written and oral communication skills. ? Should have effective time-management skills and be highly organized ? Should be adaptable and flexible to meet changing needs 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. 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[Premiere Biotech company in Sorrento Valley is seeking a Packaging Design Engineer to join their team for 3-6+ months. **Please submit your word formatted resumes for a call today! Job Description: Requirements: BA or BS in Packaging Engineering and 2-5 years related experience Experience with In Vitro Diagnostics Highly Desired •Package engineering, component testing, and approval of documentation processing for packages of medical device (Molecular Diagnostic products) •Creates, maintains and organizes routine Package Engineering documents. •Reviews Engineering documents for completeness. •Enters documents into internal document control system to assure cGMP, ISO, distribution, and product stability requirements are met. •Monitors documents through review and approval cycle. •Obtain materials and components for packaging testing requirements •Maintains Engineering specific databases. •Draft and process Test Protocols to make use of Department SOPs and assembling test materials for delivery to and coordination with outside test labs. •Prepare/process existing company approval documentation through revised company systems. ]]>

<![CDATA[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 Project Manager will be a key member of the Project Management team, reporting directly to the Vice President of Project Management. The Project Manager will be responsible for assisting the VP in the development and management of project timelines and tracking and monitoring milestones and key dates. Primary Responsibilities: • Assist VP in the developing, identifying and monitoring project plans, resources, timelines and budgets with adherence to corporate objectives and project plans • Track milestone achievements and monitor key dates • Communicate regularly with milestone champions and inform VP in advance of key achievements and if there is a potential of a delayed achievement date • Develop and prepare agendas, presentations • Facilitate project team meetings as needed and ensure invitee list includes all relevant participants, take minutes during senior meetings, make sure assigned deliverables and duties emerging from the sessions are known and track the completion of deliverables • Analyze contracts (MTAs, CDAs, etc) and proposals and identify potential issues in advance and suggest measures to mitigate and/or manage risks • Prepare and issue requests for proposals, schedule presentations as needed, and summarize proposals for executive team/VP. • Keep executive team/VP informed of current and anticipated expenses of key contracts. May troubleshoot invoices and work with internal accounting staff and vendors to correct any problems • May manage vendor relationship and expectations and builds a collaborative relationship with the vendor • Review and write business correspondence • Research potential funding sources to coincide with the funding focus of the company • Manage the grant funding budget and accounting process as needed Requirements: • BS required, MS preferred • Requires 2-5 years related project management experience, preferably in the life science industry • In depth knowledge of Microsoft Project and Microsoft Project Server required • Detail oriented and extremely organized; ability to prioritize multiple project deliverables • Strong mathematical/financial skills • Ability to multi-task and prioritize efficiently across multiple projects/sub-projects • Strong analytical and interpersonal skills, as well as the ability to motivate and influence; vendor interface experience and strong negotiating skills • Excellent written and oral communication skills • Ability to multitask and work both in a team environment as well as independently as required • Ability to handle details of a highly confidential and critical nature • Proficiency with Microsoft Office products, in particular Word, Excel, PowerPoint, Outlook and Visio 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[Genoptix, located in Carlsbad, CA, is more than just a company--we are a team of highly trained professionals working together to optimize patient outcomes. We specialize in hematologic malignancies, disorders, and subtypes in bone marrow, blood, and lymph nodes, with expertise in the most challenging diagnoses. We also specialize in solid tumor workups using molecular testing. Currently, we have an opening for an Associate Scientist/Scientist. Summary Genoptix BioPharma Services, a part of Genoptix, Inc., works to support assay development for the Genoptix clinical assays as well as perform clinical trials through full-service hematology/oncology testing. Our esoteric laboratory combines a highly trained professional staff with sophisticated instrumentation for optimal test efficiency and quality control. We focus on providing high-level, personalized services to our clients to aid in biomarker assay development, patient eligibility/stratification in Phase I-III clinical trials, efficacy endpoints, and lab results interpretation. As part of these services, we are expanding by creating FDA regulated Companion Diagnostic products to be used in our clinical laboratory. Among other duties as described below, the incumbent will assist in technology transfer validation and be the lead scientist developing appropriate FDA quality and compliance parameters for laboratory developed assays Essential Duties & Responsibilities Note: Other duties may be assigned. •Perform various molecular assays in accordance with CLIA and FDA requirements. •Design, execute and troubleshoot experiments independently •Prepare SOPs and internal reports. •Generate component and assay specification via testing and guard band validation studies. •Qualify reagents, maintain instruments and prepare associated documentation. •Ensure that any FDA product related changes or improvements in components, processes, software and equipment follow FDA Quality System Regulation (QSR) requirements. Qualifications •Hands-on experience with nucleic acid technologies within a regulated setting is required. •Assay validation and technology transfer experience. •Solid understanding of FDA Quality System regulations, with medical device experience desirable. •Must have meticulous attention to detail, be highly organized, with proficient reasoning skills in experimental design, data analysis and interpretation. •Ability to work independently as well as in a team environment. •Excellent written and oral communication as well as interpersonal skills. •The candidate must have an expectation, desire and proven ability for providing quality work. Education and/or Experience Requires a Bachelors or masters degree in molecular or cell biology, immunology, oncology or related field. 4+ years of relevant industry experience working in a regulated laboratory. Licensed Clinical Molecular Genetic Scientist (full CLS or limited license CGMBS) or California approved Medical Technologist (ASCP) a plus. The company offers a competitive salary package with benefits including vacation and sick pay, extensive insurance coverage, flexible spending accounts, 401 (k) match, employee stock purchase plan, tuition reimbursement, and more. Genoptix is more than just a laboratory – we deliver actionable results to improve patient care. If interested, please apply online to the following link: <a href="http://tbe.taleo.net/NA4/ats/careers/requisition.jsp?org=GENOPTIX&cws=1&rid=582" rel="nofollow">http://tbe.taleo.net/NA4/ats/careers/requisition.jsp?org=GENOPTIX&cws=1&rid=582</a>]]>

<![CDATA[Our company is an environmental sciences, planning, and engineering consulting firm seeking a Lab Manager to oversee our Toxicology lab for our Carlsbad, CA office. The ideal candidate will have a bachelor’s degree in Environmental Science or related field, and a minimum of 3 years experience. Senior level technicians are encouraged to apply, as we will provide management training! Requirements: - Bachelors degree in Geology, Biology, Environmental Science, Environmental Engineering, or related field (advanced degrees welcomed). - 2-5 years experience in Phase I ESAs and soil/groundwater assessment/remediation. - Excellent verbal and written communication skills. - Field capabilities including logging borings, collecting soil and groundwater samples, and mapping and collecting soil samples for large remediation projects. - OSHA health and safety training for hazardous waste sites. - Well-organized, analytical, hard-worker, sense of humor, and good team player/leader. - Prior experience working on assignments under regulatory agency oversight including local agencies (i.e. County DEH, LADPW, other CUPAs, etc.), State organizations (RWQCB, DTSC) and/or the Federal EPA. This is a direct hire opportunity that offers a competitive salary and benefits. We will consider non-local candidates, though there is no relocation assistance. If you are interested in applying, please send your resume to sandiego@labsupport.com. Thank you. ]]>

<![CDATA[NovaRx is a biopharmaceutical corporation located in Sorrento Valley. Our mission is to develop therapeutic vaccines to cure cancer and enhance patient quality of life. We are currently looking for a Research Associate to work in our R&D Stem Cell department. The individual is responsible for performing cell-based assays to support our cancer vaccine program. The individual should be familiar with tissue culture, flow cytometry and immunological assays. Responsibilities & Duties: 1. PERFORM CELL CULTURE, TRANSFECTION, FLOW CYTOMETRY ANALYSIS (FACS), ENZYME-LINKED IMMUNOSORBENT ASSAY (ELISA) AND CELL-BASED IMMUNOLOGICAL ASSAY. 2. Record experimental procedures and results accurately and clearly in lab notebooks. 3. Comply with company safety policies and minimizes risk to self, others and the environment, consistent with the community and industry standards. 4. Actively pursue corporate timelines and milestones set by the department director and upper management. 5. Other duties as assigned. Requirements: 1. A Bachelor’s or Master’s degree in the biological sciences with a minimum of at six years cancer immunology experience. 2. Strong technical background in cell biology and immunology. Experience working with cell culture, FACS and ELISAs. 3. Familiarity with Word, Excel and Powerpoint.. 4. Knowledge and experience with DNA immunochemistry techniques and PCR is a plus. 5. Experience in GLP and experimental procedures record keeping requirements. 6. Demonstrated dedication, communication and teamwork are essential. 7. Ability to work independently with minimal supervision in a team based environment. 8. Good verbal and written communication skills. 9. Ability to work calmly and effectively in a fast paced, dynamic environment. LOCAL CANDIDATES ONLY. THIS IS A TEMPOARY POSITION FOR APPROXIMATELY 8 MOTHS. MAY BE EXTENDED.]]>

<![CDATA[Do you love working in a continuous busy environment?? If you do and don’t want to worry about lay-offs, this is the place for you! These positions are for 1st shift. You must be able to work a flexible schedule. Do you have the following? • Recent manufacturing experience • Assembly and/or microscope experience is a plus • Ability to sit/stand up for an entire shift if required • Clean room experience preferred These are long-term assignments, POSITIONS START IMMEDIATELY. Apply in person between the hours of 8AM and 3PM for consideration at: Eastridge Light Industrial 10717 Camino Ruiz, Suite 252 San Diego, CA 92126 PLEASE BRING A COPY OF YOUR RESUME. ]]>

<![CDATA[ Are you an experienced Quality Control Inspector? BUSY and GROWING medical device manufacturer is looking for EXPERIENCED inspectors to start as soon as possible! To be considered for these positions you MUST have the following: - recent experience (last 2 years) in manufacturing - experience in laboratory environment - experience working with and around chemicals such as mixing and testing solutions - excellent experience working with data collection - strong computer and documentation skills - microscope experience a MAJOR plus - be able to work overtime and Saturdays as needed If you have the above experience and want to get to work tomorrow, APPLY TOMORROW!!! Eastridge will be accepting applications in person from 8AM to 3PM for these positions. Apply in person at: 10717 Camino Ruiz, Suite 252 San Diego, CA 92121 Remember you MUST have the above experience, be able to pass a background check with NO incidents, and bring 2 forms of identification to show you are able to work in the United States. WE LOOK FORWARD TO SEEING YOU!!!]]>

<![CDATA[Synedgen, Inc is biotechnology company developing new biomaterials for use in anti-infective clinical and non-clinical pharmaceutical applications. We currently have an opening for a Senior Regulatory Affairs Manager. Overall Responsibilities: Responsible for managing regulatory affairs for the development of drug FDA regulated products through CDER, managing regulatory compliance, evaluating regulatory issues and providing accurate and timely recommendations and alternatives, as needed, to management and functional business units. Serves as a team leader on the development and submission of IND and NDA applications, control and management of documents and binders, as well as providing oversight on clinical trials, toxicology requirements and CMC documentation. This individual interacts with FDA and must have a firm command of regulations and guidelines pursuant to federal, international and corporate regulatory requirements and standards. Experience with international product registration is beneficial. • Act as the regulatory project manager for IND and NDA document preparation and compliance, amendments, binders, supplements, annual reports, control documents, etc., for FDA submissions to CDER. • Interact effectively with functional business units in order to coordinate and facilitate documentation required for submissions, ensuring that timelines are met. • Mentor other associates in proper documentation and regulatory compliance including review change requests and the preparation of FDA submissions. • Participate and contribute to strategic planning for multiple submissions to CDER and leveraging of previous IND and NDA components • Evaluate changes to regulatory documents, updates, FDA requests and formulates strategies to maintain submission goals. • Assure timely submissions and expeditious approvals. Successful applicant will demonstrate: • Strong critical and logical thinking. • Thorough knowledge of all FDA requirements pertaining to the control and submission of regulatory documents for drug approval • Excellent organization skills and the ability to multi-task; detail oriented. • The ability to establish and maintain good working relationships at all levels of the company and with external contacts. • Excellent verbal and written communication skills. Share concepts, ideas, information, and suggestions with management, peers and others. • The ability to evaluate regulatory documents and determine appropriate action. • The ability to provide regulatory assessment to other departments with little or no supervision. REQUIREMENTS: • Minimum of a Masters degree or 5 years industry experience; PhD preferred • A minimum of 4 years of full-time regulatory FDA drug experience • Demonstrated experience in project management and FDA documentation • A working knowledge of FDA and regulations and how to interpret and monitor updates with experience or knowledge in US Title 21 CFR Parts 300-314 Subchapter D—Drugs for Human Use • Domestic and international travel may be required. • Must be willing to relocate. For consideration, submit FULL resume and contact information for three references. ]]>

<![CDATA[Adecco Medical and Science, a division of the world leader in the recruitment of medical and scientific professionals, has an immediate opening for a Production Scientist on a 6-12 Month contract opportunity in Carlsbad, CA. Responsibilities: - Provide technical support, perform experiments, and analyze results for the preparation and characterization of avidin, latex, latex particle characterization and reagent production - Participate on teams to review and assess process improvements and production processes for reagent formulation. - Activities will ultimately aim to improve production consistent with business objectives of quality, cost and service Requirements: - Bachelor’s Degree in Life Science, preferably Chemistry, Biochemistry or Molecular Biology - 0-3 years of relevant experience in diagnostic manufacturing environment - Understanding of Quality Systems Regulations and compliance - Proficient in Microsoft Word and Excel - Good communication skills Entry-level candidates are encouraged to apply. The Adecco Group is a Fortune Global 500 company and the global leader in HR services. Our group connects over 700,000 associates with our business clients each day through our 6,600 offices in over 70 countries and territories around the world. We offer employment opportunities at any stage in your professional career. Contact us today to discuss available contract and direct hire positions. Adecco Medical and Science offers benefits including Tuition Reimbursement, 401(k), and Insurance Benefit Plans. Adecco Medical and Science is an Equal Opportunity Employer.]]>

<![CDATA[La Jolla Institute for Allergy & Immunology (LIAI) www.liai.org Please apply directly to: <a href="https://home.eease.adp.com/recruit/?id=521808" rel="nofollow">https://home.eease.adp.com/recruit/?id=521808</a> Job Summary: The Grant & Contracts (G&C) Specialist will facilitate the administrative processes for preparation and submission of all agency sponsored grant proposals and applications as well as assist with the post award administration of grants and contracts awarded. The G&C Specialist will work directly with faculty, research staff, internal departments and management to collect all required information while adhering to sponsor agencies policies and guidelines. Job Responsibilities: • Responsible for performing the pre-award administrative duties of grants and contracts submitted to federal (primarily NIH), state and local government and private funding agencies. • Responsible for post-award administration of grants and contracts awarded from federal (primarily NIH), state and local government and private funding agencies. • Responsible for the development and administration of subawards/subcontracts/consortium agreements/other sponsored research agreements. • Apply specialized knowledge and interpretation of rules, regulations, policies and procedures from funding agencies and combine those with LIAI policies. • Exercise independent judgment and discretion in the management of grants and contracts. • Some examples of duties include: responding and preparing grant/contract/fellowship applications to be submitted to said agencies, responding to JIT requests; reviewing and interpreting funding documents; researching, interpreting and applying appropriate funding agency regulations as required by each award; maintaining contact with funding agencies regarding budget changes, no-cost extensions; establish budgets for Grants and Contracts Department & Accounting; reviewing, analyzing and preparing reports; maintain documentation for audits; grant/contract closeout. • Responsible for communicating and maintaining “good news” and funding opportunities announcements on internal website • This above incorporates the most typical duties performed. It is recognized that other related duties not specifically mentioned may also be performed. Minimum Qualifications: Bachelor's Degree in Business Administration or equivalent and three years progressively responsible professional experience in sponsored research administration; excellent written and verbal communication; advanced computer skills; capacity to function calmly and efficiently in stressful situations which require tact and diplomacy; a high level of flexibility and analytical ability. Standard Requirements: The ability to report to work on time; follow directions from a supervisor; interact effectively with co-workers; understand and follow posted work rules and procedures; accept constructive criticism; for managers and supervisory personnel to lead and manage others; and to maintain a positive work atmosphere by acting and communicating in a manner so that you get along with research personnel, co-workers and management. Preferred Education/Certifications: Familiarity with Federal guidelines (specifically, the NIH Grants Policy Statement, Circular A-122, A-110 and A-133). Please apply directly to: <a href="https://home.eease.adp.com/recruit/?id=521808" rel="nofollow">https://home.eease.adp.com/recruit/?id=521808</a> ]]>

<![CDATA[ San Diego Biotech company looking for an accountant with specific experience in inventory accounting, sales order entry, and related functions, using QuickBooks and AdvancePro. Position is approx. 30 hours per week, with no benefits, but can lead to a full-time position with benefits. Salary open.]]>

<![CDATA[Sapphire Energy was founded with one mission in mind: to change the world by developing a domestic, renewable source of energy that benefits the environment and hastens America’s energy independence. 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… or what we like to call “Green Crude”. The goal is to replace conventional gasoline, diesel, and jet fuel. From the start, our goal has been ambitious: to become the world’s leading producer of renewable fuels and petrochemical products and now we are on the verge of creating a whole new industry…we hope you will join us! We are seeking a Senior Research Associate for a leadership position in our San Diego Upstream group. Responsibilities include, but are not limited to: • Design and execute experiments to modify microbial metabolism, including high-throughput cloning and expression analysis. • Develop assays and criteria for characterizing modified microorganisms. • PCR, cloning, and sequence analysis. • RNA purification and cDNA library preparation. • SDS-PAGE and Western blotting. • Manage team research projects in the short and long term, • Make and record detailed observations, analyze data, and interpret results on an ongoing basis. • Work within a team in order to achieve departmental milestones. Requirements: • Bachelor’s or Master’s degree in biology, microbiology, molecular biology, or related field, plus at least 7 years of applicable industry experience. • 2+ years proven successful experience in a team leadership/management position • Exceptional organizational and time management skills. • Demonstrated ability to independently design, execute, troubleshoot and interpret data and experiments. • Creativity and the ability to work in an interdisciplinary team in order to achieve technical and business milestones. • High quality interpersonal and communication skills are extremely important. • Proficiency in writing and oral presentations. 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. LOCAL SAN DIEGO CANDIDATES SEND RESUME DIRECTLY TO: Karen Wise Senior Recruitment Consultant for Sapphire Energy No Third Party Recruiters No Phone Calls Please ]]>

<![CDATA[The QA Validation Engineer is responsible for: 1. Generating new validation protocols. 2. Writing and assembling validation reports for approval. 3. Reviewing and approving validation documents; analyzing data, ensuring completeness and accuracy of both data and report contents. 4. Identifying validation requirements for equipment, processes and analytical methods for company and customers. 5. Participating in Technology transfer projects, ensuring compliance with cGMP's, QSR, ISO and customer requirements. MINIMUM REQUIREMENTS: 1. Bachelor Degree in Life Sciences or Engineering, or five years experience in the Biotech/Pharma industry along with some college level science or engineering classes. Aseptic processing experience is preferred; 2. Two years validation experience; 3. Knowledge of GMP's, QSR's and ISO's; 4. Ability to investigate and troubleshoot equipment and processes; 5. Technical writing experience. Excellent documentation and record keeping skills. Strong organizational and communication skills; 6. Person must be analytical, detail oriented, able to keep a timeline, self-motivated and computer literate (Word and Excel) 7. Team player, customer service oriented, willing to learn and able to work flexible hours when necessary. Validation Consultant qualifications 3 to 4 years Validation experience in medical device or pharmaceutical industry with specific hands on experience in validating the following equipment: Depryogenation ovens Clean steam autoclaves Lyophilizers Temperature mapping of storage areas (freezers, cold boxes) ]]>

<![CDATA[Job Title: Research Associate I Job Number: 0132050810 * Please submit resumes to jobs@arenapharm.com and indicate the job number (0132050810) in the subject line. Description: This position requires a bachelor's degree in biological sciences and 6 months to a year of experience with cell-based assays in either the drug discovery industry or academic setting. Strong communication and computing/instrumentation skills are required. The position requires a strong sttention to detail and a high level of self-motivation. Essential Duties and Responsibilities: • Executing cell-based assays for GPCRs • High throughput screening • Data entry, QC and analysis • Tissue culture • Use of automation/robotics Job Requirements: Education: BS in Biological Sciences Experience: 6 months to a year of experience with cell-based assays in either the drug discovery industry or an academic setting Specific Skills: Some experience with tissue culture and running cell-based assays, particularly those relevant to GPCRs; strong computer skills and experience with laboratory automation; strong attention to detail and a high level of self-motivation Supervisory Responsibilities: None Physical Demands/Work Environment: This position will require working in a laboratory environment the majority of the time and working at a desk, computer/keyboard for the remainder. ]]>

<![CDATA[A Biotech company located in Sorrento Valley is looking for a Part Time Research Associate! (25-30 hrs/wk) The mission of this company is to deliver innovative drugs for the treatment of cancer and other severe, immune, inflammatory conditions. Department: Pharmacology Responsibilities: Assist scientists with the evaluation of small molecules in pharmacology studies. Perform ELISAs on samples from various studies. Analyze and plot data using graphing software. Qualifications: *Needs to have in-vivo experience * Requires higher level course work in biology/immunology/physiology or a bachelors degree in biology or equivalent discipline and 1-2 years of experience * Must be proficient with small animal handling and compound dosing * Familiarity with running ELISAs would be preferred * Proficiency with Excel and Word required * Must have good communication skills and the ability to work in a team-oriented environment Please email your resume today!]]>

<![CDATA[Pharmatek Laboratories, Inc. is a premier pharmaceutical chemistry development organization supporting the pharmaceutical and biotechnology industries. Pharmatek focuses on bringing client drug compounds from discovery to the clinic with services that include compound selection, analytical development, preformulation testing, formulation development, GMP pharmaceutical manufacturing and stability storage and testing. A QC Analyst I is responsible for performing various analytical techniques and common standard lab practices in order to assess the quality of pharmaceutical products under cGMPs and limited supervision. This entry level position gives opportunities to broaden GMP expertise and learn the common operations in a fast-paced, dynamic Quality Control group. The desirable applicant will have the following: • BS degree in Chemistry or other applicable scientific discipline • Strong written and oral communication skills • Extremely well organized, have excellent time management and multitasking skills • PC and Microsoft Office proficient • 0-3 years of experience in Quality Control following cGMPs • Understanding and/or experience with the following analytical equipment: HPLC, UV/Vis, balances, pH meters, Karl Fisher, disintegration baths and dissolution apparatus Responsibilities include, but are not limited to: • Analysis of pharmaceutical products, including the set-up and execution of GMP in-process, release and stability testing using a variety of analytical techniques • Creation of stability data sheets and Certificates of Analysis to summarize analytical testing • Participation in the evaluation and qualification of analytical methods • Participation in Out of Specification investigations and the writing of analytical variances • Ensuring that stability samples are pulled from chambers at the appropriate intervals and tested within the testing windows specified by SOPs and protocols • Participation in revision of protocols and test methods • Understanding of cGMPs, Pharmatek SOPs and Pharmatek systems applicable to work performed Pharmatek offers a competitive compensation and benefits package, and an outstanding team environment. PLEASE APPLY ON-LINE, USING THE CAREERS PAGE OF OUR WEBSITE: www.pharmatek.com ]]>

<![CDATA[Advanced Brain Monitoring, Inc. located in North County, having a unique diversification of Department of Defense contracts and medical device manufacturing is seeking a part-time (20-25 hours per week) Product Development/Manufacturing Associate. The individual must be detail oriented, very well organized, a team player and able to handle multiple tasks at once. The ideal candidate has a college degree, along with a strong work history demonstrating relevant experience in the following areas: • Creation and execution of hardware and software validation plans • Assist with the development of new products • Follow and develop written instructions for manufacturing processes • Maintain quality system documentation for manufacturing and new product development • Coordinate purchasing and manufacturing with vendors • Assembly and kit final product • Ability to handle multiple tasks and projects as assigned Qualifications: • Bachelor’s degree (preferably in Computer Science, Engineering, Biotech) and 2-4 years of work experience required. • Experience in a research and development environment including data analysis preferred • Prior software troubleshooting preferred • Organized, detail oriented • Strong verbal and written communication skills • Must be comfortable in taking the initiative • Strong problem solving skills • Must establish through work history the ability to be self-managed, multi-task, handle conflicting priorities, and adapt rapidly to new projects. • Individual must wish to continually learn new skills and perform new tasks. Salary: $15.00 per hour ]]>

<![CDATA[Research Associate (Part-Time) Responsibilities: Assist scientists with the evaluation of small molecules in pharmacology studies. Perform ELISAs on samples from various studies. Analyze and plot data using graphing software. Qualifications: Requires higher level course work in biology/immunology/physiology or a bachelors degree in biology or equivalent discipline. Must be proficient with small animal handling and compound dosing. Familiarity with running ELISAs would be preferred. Proficiency with Excel and Word required. Must have good communication skills and the ability to work in a team-oriented environment. Note: This position will be approximately 6 hours per day, M-F. ]]>

<![CDATA[We are a rapidly growing pre-owned scientific instrument and service company located in San Diego with a customer base all around the world. We are looking for a service engineer/technician who is experienced working with analytical instruments. Ability to service and repair HPLC and LCMS systems is highly desired. The position is intended to be a full-time; however, a part-time appointment is also an option. If interested, please reply with your resume that details the brand and models the instruments you have serviced. Please also indicate your salary requirement.]]>

<![CDATA[Scientist, Strain Evaluation Sapphire Energy was founded with one mission in mind: to change the world by developing a domestic, renewable source of energy that benefits the environment and hastens America’s energy independence. 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… or what we like to call “Green Crude”. The goal is to replace conventional gasoline, diesel, and jet fuel. From the start, our goal has been ambitious: to become the world’s leading producer of renewable fuels and petrochemical products and now we are on the verge of creating a whole new industry…we hope you will join us! We are seeking a motivated Scientist to join the Strain Evaluation team in San Diego, CA. Responsibilities include, but are not limited to: • Evaluate and characterize algae strains in the lab using various autotrophic growth systems. • Develop and troubleshoot efficient high-throughput methods for testing cultures at various environmental conditions, and assemble protocols and SOPSs for newly developed methods. • Supervise research projects in the short and long term, and manage a small team. • Analyze data, prepare scientific reports and presentation, and communicate to co-workers in various regular and on-demand forums. • Fulfill certain weekend duties. Requirements: • Ph. D. with 2-5 years relevant work experience, or M.S. with 4-8 years relevant work experience, is required. • Proficiency with sterile technique and microbiological culture is required. • Proficiency with light microscopy is required; experience with fluorescence microscopy is preferred. • Prior knowledge and experience in the areas of cell biology, microbiology, photosynthesis, plant nutrition, plant protection, and/or algal physiology is preferred. • Proficiency in Excel environment is required, and experience with a LIMS or programming proficiency (VBA, etc.) is preferred. • Proven ability to design and supervise research projects, prioritize daily and long term tasks, and manage research team in a fast-paced environment is required. • Must be a detail-oriented and organized scientist, and able to prepare scientific reports and present data to coworkers and management • Due to the collaborative nature of the position, interpersonal communication skills are extremely important 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. Qualified candidates please send your complete resume to: Mary Lynch Senior Recruiter Sapphire Energy mlynchhr@yahoo.com ]]>

<![CDATA[Principal Industrial Microbiologist Sapphire Energy was founded with one mission in mind: to change the world by developing a domestic, renewable source of energy that benefits the environment and hastens America’s energy independence. 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… or what we like to call “Green Crude”. The goal is to replace conventional gasoline, diesel, and jet fuel. From the start, our goal has been ambitious: to become the world’s leading producer of renewable fuels and petrochemical products and now we are on the verge of creating a whole new industry…we hope you will join us! We are seeking an energetic, results-oriented Principal Industrial Microbiologist to join our R&D team. You will work on the development of processes for outdoor growth of microalgae, including media development, growth optimization, and contamination prevention and control strategies. Responsibilities include, but are not limited to: • Development of processes for growth of microalgae, including media development, growth optimization, and contamination prevention and control strategies. • Design and execute experiments; analyze data and interpret results; communicate results to other members of the R&D team. • Management of a development team focused on the above. • This position will interact with the molecular biology, strain development, technical and engineering operations, field piloting, and analytical departments. • Recruit and train of new scientists and research associates. • Provide example of professionalism for the laboratory staff. Requirements: • Advanced degree (M.S. or Ph.D.) in Microbiology, Environmental Microbiology, Microbial Physiology, Microbial Ecology, Chemical Engineering, Molecular Biology, Biochemistry or related discipline. • 7+ years of R&D experience, minimum 5 years in microbial fermentation industry • 3+ years of demonstrated leadership, strategic capabilities, and management experience in biotechnology. • Knowledge and understanding of cell biology, media development, mass and energy balance is essential. • Scale-up experience of commercial fermentation processes. • Deep specialized knowledge in one or more of the following areas: strain development, fermentation principles and operations, biochemistry, enzymology, metabolic engineering, or microbial physiology. • Track record of developing and delivering biotechnology solutions for multiple businesses or industries. • The ability to work in a project-oriented environment and interface effectively with other groups in the company is essential. • Excellent oral and written communication skills. • Experience in managing complex processes. 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. Qualified candidates please send your complete resume to: Mary Lynch Senior Recruiter Sapphire Energy mlynchhr@yahoo.com ]]>

<![CDATA[Microbial Physiologist Sapphire Energy was founded with one mission in mind: to change the world by developing a domestic, renewable source of energy that benefits the environment and hastens America’s energy independence. 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… or what we like to call “Green Crude”. The goal is to replace conventional gasoline, diesel, and jet fuel. From the start, our goal has been ambitious: to become the world’s leading producer of renewable fuels and petrochemical products and now we are on the verge of creating a whole new industry…we hope you will join us! We are seeking an exceptional Microbial Physiologist to join our Microbiology staff in San Diego, CA. Responsibilities include, but are not limited to: • Physiological characterization of strains of algae under a variety of conditions. • Identification of growth conditions that optimize growth of algal strains of interest. • Creativity and the ability to work within and lead a team in order to achieve technical and corporate milestones. • Collaborate with section-level peers • Provide example of professionalism and proficiency for the laboratory staff. Requirements: • Doctoral degree in microbiology, biology, molecular biology, experimental evolution or related field plus at least one year post-doctoral experience. • Experience in microbial physiology is essential: o Significant experience with methods for characterizing and understanding growth properties o Capable of rapidly analyzing large data sets; experience with programming languages / statistical software • Experience with microalgae a plus. • Strong leadership and organizational skills. • This position will work closely with both research and development. The ability to concisely and effectively communicate results will be extremely important. • Ability to participate in interdisciplinary teams. • Critical thinking and problem solving skills. • Demonstrated ability to independently design, execute, troubleshoot and interpret experiments. • Proficiency in written and oral presentations. 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. Qualified candidates please send your complete resume to: Mary Lynch Senior Recruiter Sapphire Energy mlynchhr@yahoo.com ]]>

<![CDATA[Part-time Protein Biochemist Position Available: Protein biochemist with experience in protein chemistry and Molecular Biology at the level of MS/PhD. or BS with relevant experience also will be considered. Requirements: At least two years lab experience in protein expression in multiple systems; Protein purification preferable with either AKTA and/or BioRad systems; Good notebook recording of experiments and protocols is a key requirement; He/she must have good writing skills.]]>

<![CDATA[Associate Product Manager (Temp 3-6 months) (Job Code IM016) 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 currently looking for a self-motivated individual to cover the leave period for one of our Associate Product Managers. In this position, you would 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 not only be hardworking, but detail oriented and a quick learner. Responsibilities include: • 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) This position is located in our corporate office in San Diego’s biotech community. Please reference job code IM016. ]]>

<![CDATA[Immediate, Part-time, Virtual: Use your interest, knowledge, and research skills to earn between $5,000 and $50,000 per research project. Earn potential rewards for uncovering scientific technical documents and develop valuable research experience. Article One Partners is the world’s largest patent research community. Article One posts requests for articles, patents, research papers, product literature, or any publicly available document in any language from anywhere in the world that describes particular technologies as of a specific date. These research postings are called Patent Studies, and the requested information is known formally as prior art. Article One’s global research community submits prior art in response to the posted Studies. By researching and submitting prior art, Article One’s registered members or Researchers become eligible to receive the stated reward. Rewards are distributed when Article One determines that a Researcher’s submission best matches the requirements of the Study as stated in the Study description. Anyone can join Article One’s global research community. Register as a Researcher at <a href="http://www.articleonepartners.com" rel="nofollow">http://www.articleonepartners.com</a> and begin working on these and other Studies: • Two-Sided Printable Media ($5,000) • Method of Manufacturing: Semiconductor Devices ($5,000) • Data Processing Device: Semiconductor Chip ($5,000) • Adding Function to a Web Page ($10,000) • Communication of Selected Information ($20,000) • Hydraulic Gear Pump Having Sound Absorption Cavities ($15,000) • Dynamic Power Management Device ($10,000) • Wireless Device: Multi-Function Communicator ($5,000) Article One will review all submissions and inform you if you have earned the stated reward. Your active participation on Article One will earn points for profit-sharing, as described on our website. For more information or to register as a Researcher, visit <a href="http://www.articleonepartners.com" rel="nofollow">http://www.articleonepartners.com</a> When registering, please enter the referral code “craig.”]]>

<![CDATA[We are an ISO Certified leading bulk manufacturer of high quality proteins and immunoreagents for the diagnostic industry and research community. Due to continued growth we are looking to add a manufacturing associate to our team. We are a privately held company located in the Sorrento Mesa area. We are proud to offer competitive compensation, above average benefits and an outstanding work environment with opportunities for you to learn and grow with our company! Our ideal candidate will be self-motivated, able to multi-task and meet timelines efficiently and productively while demonstrating the ability to learn new techniques. The following will be the primary responsibilities for this position: • Preparation of general laboratory buffers and reagents • Assist in protein purification activities • Perform analytical and process methods related to protein purification processes • General Laboratory tasks including but not limited to ordering laboratory supplies, maintaining laboratory equipment, and general laboratory upkeep Required Qualifications & Experience: • B.A. or B.S. degree in Chemistry, Biology, Biochemistry, or related fields with 2 years experience or a minimum of 5+ years of experience in a laboratory manufacturing setting. • Fundamental knowledge and training in the area of Biological Sciences including Chemistry and Biochemistry • Physical ability to carry on operations of large scale production processes including the ability to lift up to 50 lbs • Ability to work independently • General knowledge of Laboratory safety • Strong verbal and written communication skills • Strong Computer Skills Preferred Experience: • Use of a broad range of laboratory equipment • Knowledge of methods relevant to protein purification (Salt Fractionation, Clarification, Buffer Exchange, and Liquid Chromatography Techniques) • Knowledge of Analytical Methods relevant to protein purification (Protein Assay, Enzyme Assay, Immunoassay, and Gel Electrophoresis techniques) • Knowledge of ISO or QSR Please submit your Resume, salary history and salary requirements for immediate consideration ]]>

<![CDATA[Leading biotech company has an opening for a Manufacturing Tech III. Will be responsible for the reagent/lab supply preparations and supporting manufacturing of Diagnostic materials. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties as assigned. Manufacture of In-House material, such as Reagents, Controls, Standards, ELISA plates, IFA slides, etc. Sera acquisition Inventory maintenance of materials Lab organization and maintenance Equipment operation, maintenance, troubleshooting, and possibly repair. Write department specific documents (Manufacturing batch records, procedures, incoming material specifications) Submission of Document Change Requests (DCR) for documents. Recognition of non-conformance (NCMR) and ability to complete required documentation to address NCMR. Investigate issues with ability to identify root cause. Implement actions to close CAPA. Generate reports/memos such as investigation reports, issue review, memos Operate per cGMP guidelines. Scheduling of Reagent builds. Identify and implement changes to reduce cost, improve product quality, improve product robustness, etc. EDUCATION and/or EXPERIENCE Position generally requires a High school diploma or general education degree (GED) and 5+ years related experience. Experience working in GMP or CLIA laboratory environment preferred. Please submit your resume for immediate consideration. ]]>

<![CDATA[Part-time. Well known pharmaceutical company seeks candidate to work 25-30 hours per week assisting scientists with the evaluation of small molecules in pharmacology studies. Performs ELISA on samples from various studies. Analyze and plot data using graphic software. Requires higher level course work in biology/immunology/physiology or a bachelor's degree in biology of equivalent discipline. Must be proficient with small animal handling and compound dosing. Familiarity with running ELISA's would be preferred. Proficiency with Excel and Word required. Must have strong communication skills and the ability to work in a team-oriented environment. ]]>

<![CDATA[Research Associate Primary duties include (but not limited to) assay development, isolation of primary cells from blood, surface and intracellular immunophenotyping, fluorescence and magnetic-based cell sorting and standard molecular techniques. Additional duties include performing routine lab maintenance, writing SOPs, and maintenance of a database. Other duties as assigned. Qualifications: * Bachelor's degree required/Masters desired in Biology/Cell Biology. * Minimum of 3 years experience working with blood, cell separation and tissue culture required. * The ability to function independently and on a multi-disciplinary team. * Excellent written, verbal and interpersonal communication skills required. * A research background is highly desirable. * Flexibility in handling rapidly changing goals is a must. * Demonstrated initiative and the ability to learn and adapt to new technologies a must. * Use of Microsoft Excel for data analysis.]]>

<![CDATA[Research Associate Applicant must possess a B.S. in Biochemistry, Molecular Biology or equivalent. 1 -2 years of biological or chemical laboratory experience is required. Experience with enzymes or biochemistry is a plus. Solid computer skills are required. Applicant must be adept in the use of Microsoft Excel and have experience analyzing and graphing scientific data. Knowledge of programming or VBA macros is a plus. Experience in the execution and design of automated assays and protocols is a plus. Applicant must have a strong motivation to learn to operate a wide variety of automation and scientific instruments. Applicant must be able to use simple tools such as wrenches and screwdrivers. Attention to detail is required. Excellent written and communication skills are required. ]]>

<![CDATA[The La Jolla Bioengineering Institute invites applications for a Researcher Associate position to perform research on mechanisms of pathogenesis and therapeutics of cerebral malaria in the P. berghei mouse model, using techniques such as brain intravital microscopy and protein expression by western blot. We seek a highly motivated individual with experience in animal in vivo studies. Small animal surgery skills are desired. Candidates must have completed a B.S. or M.S. degree and should submit cover letter, curriculum vitae and the names of at least three references electronically to email: hr@ljbi.org – reference RA-CLC in the subject line. LJBI offers salary commensurate with experience and benefits including: medical, life insurance, paid vacation, holidays. Equal Opportunity Employer.]]>

<![CDATA[The La Jolla Bioengineering Institute invites applications for a Post-doctoral position to perform research on the mechanisms of pathogenesis and therapeutics of cerebral malaria (PI: Leonardo Carvalho, PhD), with focus on the role of nitric oxide, using in vivo (P. berghei) and in vitro (P. falciparum) models and employing tools such as brain intravital microscopy and in vitro cell cultures. We seek a highly motivated individual, with desired experience in malaria research, animal in vivo studies and cell culture-based assays. Candidates must have completed a Ph.D. degree or equivalent and should submit curriculum vitae and the names of at least three references electronically to hr@ljbi.org – reference PR-CLC in the subject line. LJBI offers salary commensurate with experience and benefits including: medical, life insurance, paid vacation, holidays. Equal Opportunity Employer.]]>

<![CDATA[The Director, Development - Molecular Bilogy manages staff engaged in advanced product development and systems integration/support. Additionally: -- Oversee multiple projects and system interfaces. -- Manage a technical group and associated resources responsible for the definition, development, and approval of high impact product designs or processes. Responsible for implementing and maintaining the effectiveness of the quality system. -- Monitor projects across multiple product development groups or disciplines to ensure major milestones are met. -- Make final decision on project resource or capacity issues; initiate and coordinate planning and action to address those issues. -- Prepare, consolidate and manage budgets. -- Determine and approve actions to deal with variances. -- Define long term strategy for functional area. -- Review and approve proposals ensuring system integration requirements are met. -- Keep abreast of developments in technology or design methods and forecast future trends. -- Design and implement an organization that responds to the needs of the business and provides a meaningful work experience for employees. Working knowledge and hands-on experience with of microfluidics, systems integration and miniaturization, and device manufacturing is preferred. Previous management experience and skills in project management and planning are preferred. Basic Qualifications: B.S./M.S. in Engineering, Life Science or a closely related discipline and 6+ years technical experience with 8+ years of supervisory or management experience, or a Ph.D. in Engineering, Life or Physical Science, or closely related discipline and 3+ years technical experience with some supervisory or management experience. Knowledge of regulations and standards affecting IVDs and Biologics. Demonstrated advanced product development, systems integration, process design, project leadership experience and a demonstrated record of research which advances technology within the division. Must be US citizen and able to pass background investigation for eventual US Government security clearance. Preferred Qualifications: Working knowledge and hands-on experience with of microfluidics, systems integration and miniaturization, and device manufacturing is preferred. Previous management experience and skills in project management and planning are preferred. Ability to learn new techniques quickly and stay informed of new research and technologies. If interested, please apply online at <a href="http://track.tmpservice.com/ApplyClick.aspx?id=968019-1810-3593" rel="nofollow">http://track.tmpservice.com/ApplyClick.aspx?id=968019-1810-3593</a>]]>

<![CDATA[Primary Function / Primary Goals / Objectives: Senior contributor to projects focused on development and testing of portable molecular diagnostic devices. Contributes to multiple aspects of development projects including mechanical, electrical, and manufacturing. Works closely with a diverse scientific/technical group. Major Responsibilities: Responsible for implementing and maintaining the effectiveness of the quality system. Contributes to development of new concepts from initial design to market release. Conducts feasibility studies of the design to determine ability to function as intended. Maintains detailed documentation throughout all phases of research and development. Coordinates activities with outside suppliers and consultants to ensure the delivery of supplies or services needed to meet scheduled timelines. Accountablility / Scope: Operate within broad goals and objectives. Direction is provided by the goals and strategies of the product development unit or operational unit served. Contributes to multiple projects across several disciplines. Accountable for achievement of product or process design goals. Ensure policies and standards are consistent with division and regulatory requirements. Basic Qualifications: Knowledge of regulations and standards affecting IVDs and Biologics. Demonstrated advanced product development, systems integration, process design, project leadership experience and a demonstrated record of research which advances technology within the division. Working knowledge and hands-on experience with of microfluidics, systems integration and miniaturization, and device manufacturing is preferred. Previous management experience and skills in project management and planning are preferred. Ability to learn new techniques quickly and stay informed of new research and technologies. Must be US citizen and able to pass background investigation for eventual US Government security clearance. Preferred Qualifications: If interested, please apply online at <a href="http://track.tmpservice.com/ApplyClick.aspx?id=967722-1810-4193" rel="nofollow">http://track.tmpservice.com/ApplyClick.aspx?id=967722-1810-4193</a>]]>

<![CDATA[The Associate Engineer will contribute to projects focused on development and testing of portable molecular diagnostic devices. In addition, will participate in multiple aspects of development projects including mechanical, electrical, and manufacturing. Work closely with a diverse scientific/technical group. Responsible for implementing and maintaining the effectiveness of the quality system. Contributes to development of new concepts from initial design to market release. Conducts feasibility studies of the design to determine ability to function as intended. Maintains detailed documentation throughout all phases of research and development. Assists manufacturing operations in problem solving related to the prototype devices and modules. Assists manufacturing operations in problem solving related to the prototype devices and modules. Assists in the validation of process integration of modules and components. May also develop code and design system architectures in order to define user compatibility. Basic Qualifications: A bachelors degree in Engineering, Life Science or closely related discipline is required. Knowledge of regulations and standards affecting IVDs and Biologics. Ability to learn new techniques quickly and stay informed of new research and technologies is essential. Must be US citizen and able to pass background investigation for eventual US Government security clearance. Preferred qualifications: Previous exposure to microfluidics, systems integration and miniaturization. If interested, please apply online at <a href="http://track.tmpservice.com/ApplyClick.aspx?id=967674-1810-9493" rel="nofollow">http://track.tmpservice.com/ApplyClick.aspx?id=967674-1810-9493</a>]]>

<![CDATA[The Associate Scientist performs and documents molecular biology and bioanalytical procedures following existing SOPs. -- Works closely with senior researchers to optimize molecular techniques and apply them to the development of novel molecular diagnostic assays. -- Execute experiments to meet the strategic needs of the division. -- Resolve functional issues associated with prototype assays and methodologies. Optimize assays based on prior results and input from other researchers. -- Prepares reports and presents progress to management. Identifies problems, recommends appropriate action plans. Basic Qualifications: A bachelors degree in a scientific discipline such as biology, chemistry, biophycics, or related life science is required. Must be US citizen and able to pass background investigation for eventual US Government security clearance. If interested, please apply online at <a href="http://track.tmpservice.com/ApplyClick.aspx?id=967663-1810-8393" rel="nofollow">http://track.tmpservice.com/ApplyClick.aspx?id=967663-1810-8393</a>]]>

<![CDATA[Phamatech was founded in 1991 by a small group of dedicated scientists and business executives. We have grown steadily over the years to become a major provider of rapid medical diagnostic devices for home healthcare and clinical settings worldwide. Phamatech is committed to manufacturing products and providing services that enhance our customer's medical care, health awareness and quality of life by aiding in the early diagnosis of medical conditions in a cost-effective manner. We currently have two (2) positions open: one (1) Laboratory Supervisor one (1) Data Entry Clerk for the Lab OVERVIEW for LABORATORY SUPERVISOR POSITION Phamatech, Inc. has a job opening for a department supervisor in the forensic drug testing laboratory. This position involves over-seeing a graveyard shift and day shift in the specimen receipt department. Responsibilities: -Supervise the non-technical staff in receiving, processing and preparing specimens for testing in a forensic testing laboratory. -Supervise the non-technical staff in data entry of patient demographic information. -Resolve and/or address complex customer issues. -Monitor performance against the key performance indexes. -Report regularly and as needed to manager on the trends and any changes to the tactical plan to ensure successful performance. -Effectively communicate changes to direct reports. -Serve as a team leader to analyze, design, develop, implement and evaluate department procedures. Qualifications: -Forensic drug testing laboratory experience preferred. General laboratory experience required. OVERVIEW for DATA ENTRY POSITION Phamatech, Inc. has a job opening for a Data Entry Clerk position to work in our substance abuse testing laboratory. Primary Responsibility: - Heavy data entry of confidential client information Qualifications: - Must have high school diploma or equivalent. - Must have excellent and accurate data entry skills. - Must pay high attention to detail and excellent focus skills. - Strong ability to enter information into a specialized software quickly and efficiently without error. - Typing must be at least 30wpm with 10 key experience. - The chosen candidate will have excellent communication skills and proven professionlism. Phamatech, Inc. is an equal opportunity employer. Application Instructions Please state which job you are applying for in the subject line and submit BOTH an application and a resume. To retrieve our application please go to <a href="http://www.phamatech.com/application.html" rel="nofollow">http://www.phamatech.com/application.html</a> to complete application packet. Please send completed application packet along with resume to HR@phamatech.com. Incomplete application and resumes without applications will not be accepted. ]]>

<![CDATA[DexCom, Inc., a leader in continuous glucose monitoring, is headquartered in San Diego, California. Our success is built on innovation, hard work, and on seeing each other’s differences as an advantage. We are committed to developing technologies and products that improve the lives of people with diabetes. DexCom has ambitious plans to keep learning and growing – and is seeking people who have the same goals for themselves. DexCom Inc. is currently seeking a Sr. Software Engineer. Job Summary We are seeking a positive, motivated and effective Senior Software Engineer to help us develop our next generation medical device. In this position, you will have a unique opportunity to help thousands of people lead a more normal and healthy life. The individual will work in a small team of firmware and hardware engineers to develop firmware for our next generation wireless monitors. Responsibilities (other duties may be assigned) • Creates high quality algorithmic and object oriented software for an embedded device. • Architectural design of system components. • Responsible for technical ownership of issues that impact product success. • Drafts architecture, requirements, and design documents. • Develops and performs unit testing of embedded or application software. • Ability to independently determine technical solutions. • Interface with algorithm, software test, and other departments as needed. • Supports new features on previous products. Requirements • Requires a Bachelor's Degree in Computer Science or Computer Engineering from a four-year university or college. • Minimum 10 years firmware/software development experience. • Solid mathematics background. • Expertise developing system software in C++ or C#. • Experience developing and implementing scientific algorithms. • Experience or interest in developing software for an embedded device. • Familiarity with Microsoft’s Windows development tools and philosophies. • Visual Studio .Net and C# a plus. • Experience in multi-threaded application development. • Positive, motivated, effective team-oriented software developer with good communication skills. • Knowledge of medical device design and documentation a plus. About Dexcom Inc DexCom Inc. is a publicly traded company listed in the NASDAQ stock exchange. We have been FDA approved and commercially released three generations of continuous glucose monitors. 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. To apply please go to <a href="http://www.dexcom.com/careers" rel="nofollow">http://www.dexcom.com/careers</a>. ]]>

<![CDATA[Research Associate - Clinical Molecular Biology Essential Duties and Responsibilities * 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. * Support clinical specimen testing and reporting to pathologists. Qualifications * Strong background in molecular biology techniques (standard and real-time PCR, DNA sequencing, automated nucleic acid isolation, etc). * Thorough understanding of theory and operation of instrumentation used in molecular analysis. * Knowledge of statistical methods pertaining to assay quality control is desirable. * Ability to problem-solve and work independently as well as in a team environment. * Excellent written and oral communication skills. * Proficient with Microsoft Office, particularly Excel, to produce charts, graphs and spreadsheets. Education and Experience * Bachelors or Masters degree in biology, biochemistry or molecular biology, or related science field. * 5+ years of relevant experience. * Experience in clinical laboratory science, or qualification as a licensed Clinical Molecular Genetic Scientist is a plus. ]]>

<![CDATA[ Structure Based Design, Inc. is a startup biotech company in San Diego. We are currently seeking a talented and motivated X-ray crystallographer to join our team at the level of senior postdoctoral fellow or senior scientist depending on experience, qualification and your favorable project. You will participate in our diverse structural biology activities which include projects in collaboration with industry partners for drug discovery or projects in collaboration with academic laboratory for publication. Responsibilities include, but are not limited to: • protein crystallization, co-crystallization with ligands, structure determination and refinement • diffraction data collection using in house facility or synchrotron light source • high throughput gene-to-structure works including gene cloning, gene expression in different systems including E. coli, baculovirus, and mammalian cells • protein purification of recombinant proteins using His-tag, GST-tag, affinity purification, ion Exchange, hydrophobic interaction, size exclusion • prepare report and scientific publication Requirements: • PhD in experimental structural biology with post-doctoral experience • demonstrating a track record of high-quality performances on protein crystallography To apply, send your resume to hire@strbd.com • Location: Sorrento Valley • Compensation: salary will be commensurate with experience • Principals only. Recruiters, please don't contact this job poster. • Please, no phone calls about this job! • Please do not contact job poster about other services, products or commercial interests. ]]>

<![CDATA[Job Title: Research Scientist 3, Experimental Virology Reports To: Executive VP of Research & Pharmaceutical Development Position Type: Salaried, negotiable according to experience and fit; package includes company stock options, as well as tax advantaged employee benefit plans. Education and Experience Required: Requires a PhD. Degree in a scientific discipline (Virology, Immunology, Biochemistry, Microbiology or related discipline), with a minimum of 8 years of industry experience. Requires strong experimental credentials, hands-on familiarity with modern biological and virological techniques and methods. Function/Scope: The candidate will function under limited direction within a small group, and be independently responsible for the conception, design, development, execution and interpretation of scientific research projects. The platform technology of Tocagen is the use of replicative viruses as gene delivery vehicles, initially for cancer. The position is very much a hands-on experimentalist, but also requires strong intellectual interest in how viruses interact with host animals including innate immunity, along with a familiarity with applicable modern molecular and immunological techniques. The successful applicant will have a broad understanding of this area of biological research and ideally also an understanding of the principles of biological drug development. This may be a supervisory position depending on the candidate, but in any case, requires organizational interaction with other company entities. The Experimental Virology group is the engine for generating an understanding of the properties of current products, generating new product ideas and performing initial feasibility testing. The Research Scientist 3 is expected to provide an intellectual leadership role, perform experiments using his/her own and other company resources, represent the company to external entities, write proposals, grants, patents and manuscripts for publication, present work at prestigious scientific meetings and may perform special projects as required. Duties and Responsibilities Include But Are Not Limited To: 1. With limited direction, conceive, develop, and perform experiments that support Tocagen?s internal and external activities: to understand the interaction of Tocagen?s product candidates with the human body; and to develop new product candidates. 2. Develop and foster scientific expertise within Tocagen, generate collaborative or importation possibilities for accessing needed technology, provide high level intellectual input on project directions and possibilities. 3. Participate in decisions regarding the lines of scientific and medical investigation of the Experimental Virology group, and by extension the company. Contribute to decisions on company and R&D strategic directions. 4. Write reports at the appropriate quality level for internal, FDA & publication submissions. Make presentations to internal and external entities and represent the company in areas of responsibility and expertise. 5. Contribute in other scientific areas according to areas of existing expertise and company requirements. 6. Be responsible for designated equipment and reagent performance and maintenance in designated areas of responsibility 7. Perform other duties as required. General Responsibilities: 1. Operate to the highest ethical and moral standards. Comply with policies and procedures for timely completion of company, department and personal goals and objectives. 2. Be responsible for adherence to quality and safety standards set by regulations, company policy and company mission. 3. Communicate effectively with supervisors, colleagues and subordinates. Be committed to team effort and be willing to assist in unrelated job areas when called upon. 4. Plan work efficiently within the timetable of scheduled meetings, report deadlines, seminars, and limited access facilities. Coordinate with other group members and consult supervisor if conflicts arise. 5. Understand scientist?s role in meetings, be prepared to provide updates and information pertinent to your project(s), and publish manuscripts. 6. Attempt to constructively resolve any problems that interfere with scientist?s ability to perform his/her duties. Knowledge and Abilities: 1. Proven technical proficiency, scientific creativity and independent thought. Infectious disease and oncology research experience in industry of 8 years. Senior non-profit/academic experience could substitute. 2. Strong verbal and written communication skills and ability to work in a fast paced dynamic environment. 3. Excellent ?hands-on? bench and intellectual scientific skills and interest, with a desire to perform experiments. 4. Knowledge of standard laboratory operations, and expertise in a wide range of modern molecular biology, immunology and biochemical techniques. 5. Ability to read, to analyze, and to interpret general professional journals, technical procedures or governmental regulations. 6. Ability to write reports and manuals, business correspondence and professional journal submissions; ability to communicate effectively the status of projects in relationship to activities in other company groups. 7. Must be able to think strategically about scientific and project issues, negotiate and influence effectively, understand complex technical issues and be able to translate and communicate them clearly to less technical personnel. Strong collaborative, team building, and people development skills a necessity. 8. Understanding of the drug development process an advantage. ]]>

<![CDATA[The successful candidate will be responsible for ensuring that the clinical programs for ACADIA projects are executed effectively. This will include oversight, management and guidance of clinical trials. A component of the role will be to ensure quality of delivery of goals within agreed budgets and timelines. The candidate will be required to work with project leaders to ensure that appropriate resources and information are available in order that project goals are met. It will be necessary for that person to have experience in developing protocols, SOP’s, Clinical Study Reports, and other documents to support an NDA. The candidate will possess well-developed skills to select CRO’s and manage these external resources effectively. Ten (10) years of relevant clinical experience in the pharmaceutical industry, or equivalent, to include: • Experience managing staff as well as mentoring and developing junior staff. • Excellent interpersonal skills. • Demonstrated ability to lead. • Strong communication skills and the ability to create a clear sense of direction. • Knowledge and understanding of GCP and other Clinical Trial Regulations and guidelines. • Demonstrated ability to successfully develop, implement, manage and complete clinical trials. College degree required; Master’s degree preferred. ACADIA Pharmaceuticals Inc. offers a competitive compensation and benefits package, including medical, dental, vision, life, long-term and short-term disability, flex spending accounts and 401K match. If interested, please submit your resume to: hr@acadia-pharm.com.]]>

<![CDATA[ The primary responsibility of this position will be to design and execute analytical method validation and transfer studies for a recombinant protein. RESPONSIBILITIES: Author and review protocols and reports for method validation and transfers; Execute method validation laboratory activities; Review and trend existing data; Interface with CMC team; Collaborate with internal and external laboratory partners; This position is primarily laboratory based. REQUIREMENTS: Bachelor’s degree or higher; Experience working in a cGMP laboratory environment; Experience with HPLC method development and validation, spectroscopy, SDS PAGE, and other analytical techniques; Experience working with proteins. Experience writing method validation protocols and reports. Demonstrated oral and written communication skills.]]>

<![CDATA[The successful candidate will work collaboratively with Statistical Programmers, Biostatisticians, Clinical Research Associates, Clinical Data Managers and other Clinical, Global Drug Safety, Regulatory and Project Management staff to meet project deliverables and timelines for statistical data analysis and reporting. Primary duties will include: • Providing statistical consultation on trial design and study endpoints. • Calculating sample sizes and authors statistical analysis plans. • Utilizing knowledge of Regulatory requirements and guidance documents to provide statistical advice with respect to creating a clinical development program. • Using knowledge of literature to provide data analysis and presentation methods to support publications/presentations. The candidate will have five (5) to ten (10) years pharmaceutical industry experience to include lead statistical role(s) in establishment of Phase III program(s), oversight of clinical study reports, support for NDA submission, and publications. Scientific programming capability with statistical software packages is a must. Ph.D. / Masters required. ACADIA Pharmaceuticals Inc. offers a competitive compensation and benefits package, including medical, dental, vision, life, long-term and short-term disability, flex spending accounts and 401K match. If interested, please submit your resume to: hr@acadia-pharm.com ]]>

<![CDATA[ Dexcom, Inc., a medical device company, engages in the design, development, and commercialization of continuous glucose monitoring systems for people with diabetes in the United States. We are currently looking for a Sr. Process Development Engineer with medical device and/or medical diagnostics experience. The ideal candidate will have previous experience in the development, product transfer and/or manufacture of quantitative medical device products. Job Summary This position is responsible for material, process, and product improvement activities to decrease cost, improve throughput, and improve quality for current during the transfer and process development/scale-up of new products from R&D. Responsibilities (other duties may be assigned) • Interfaces with manufacturing and other departments to transfer new products into Manufacturing. • Identifies and resolves process dependant and material dependant issues within prototype configurations. • Leads/participates in process improvement projects to improve product quality, decrease cost, and improve product performance. • Analyzes prototype production and laboratory performance data to identify issues and opportunities for improvements. • Designs and executes relevant experimentation. • Writes/Executes Process and Product validations. • This role will be in the clean room 80-90% of work day. Requirements • Bachelor’s degree or higher in Chemistry, Bio-Engineering, Chemical Engineering, or related field from a four-year college or university required. • 4+ years of experience in the medical device and/or medical diagnostic field strongly preferred. • Proven track record in the commercialization and manufacture of medical devices and/or medical diagnostic products preferred • Competency in the design, execution, data and interpretation of experiment is required. • Must be able to identify key elements of multiple varying processes. • Must be able to re-design work flows to improve efficiency. • Knowledgeable in common techniques: DOE, DFSS is required. • Must be able to develop novel process and novel fixtures to develop a pilot manufacturing process. • Mechanical experience is a plus, but it is necessary to understand what the fixture “needs to do.” • Must have a high level concept of the goals of the project and be able to create workflows that achieve performance targets through process improvement. • Excellent written and verbal communication skills using MS Office (i.e. Excel and Word). • Excellent understanding of statistical analysis and experience with Minitab strongly preferred. About Dexcom Dexcom Inc. is a publicly traded company listed in the NASDAQ stock exchange. We have been FDA approved and commercially released three generations of continuous glucose monitors. 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. To apply please go to <a href="http://www.dexcom.com/careers" rel="nofollow">http://www.dexcom.com/careers</a>. ]]>

<![CDATA[Part time position availble for candidate to assist in performance of laboratory experiments and in GMP manufacturing. Requirements include an undergraduate degree in chemistry or related scientific discipline, ability to take direction, excellent writing skills and ability to work as a member of a team. GMP training is included.]]>

<![CDATA[NovaRx, a privately held biotech company located in San Diego, CA, is currently conducting a Phase III clincial trial of Lucanix™ , a non-small cell lung cancer vaccine and is in preparation for a clinical trial in glioma. We are seeking a Manufacturing Associate to assist in the manufacturing of the company’s whole cell therapeutic vaccines. This position requires previous experience in mammalian cell culture systems and will involve using scale-up technologies using multilayer static cell culture systems. Individual will be involved with both manual and automated product filling and capping machines operating in a class 100, cGMP environment. He/She is expected to fully participate in cGMP facility start-up activities working together with both Development and Quality personnel under a very aggressive production schedule. With the assistance of others, the individual will help write and revise SOPs, Batch Records and Forms. Excellent organizational skills, documentation skills and/or previous experiences in a GMP environment is a plus. Component and reagent preparation as well as some lifting and work with heavy processing equipment will be required. Responsibilities & Duties: 1 Perform manufacturing processes according to written procedures 2 Operate manufacturing equipment according to written procedures 3 Completion of manufacturing batch records and lot summary reports 4 Perform reagent and component preparations, set-up, break-down and clean-up operations 5 Ordering raw materials and supplies 6 Support process development & scale-up operations 7 Maintenance of raw material certificates of assurance and Manufacturing data basis 8 Develop and revise standard operational procedures, batch records, and forms when required 9. Other duties as assigned Techniques / Skills 1 1-4 years of previous experience in mammalian upstream production systems in a Process Development or Manufacturing environment. 2 Aseptic fill and processing using sterile connections 3 cGMP compliance trained 4 Excellent writing and communication skills 5 Excellent computer skills including Microsoft Office programs 6 Excellent organizational skills, work prioritization and follow-through ability. Strong attention to detail, accuracy is essential. Ability to be personable and professional at all times. Must have tact, diplomacy and sensitivity regarding the handling of confidential information. 7 Knowledge, operation and service of NovaBiomedical bioanalyzer and Vi-Cell instrument Education: 1 Requires BS or AA degree Please note: Local candidates only. No recruiters. ]]>

<![CDATA[Immunology Research Associate I Job Responsibilities Working in the R&D Immunology group, the Associate will assist with research and development in collaboration with internal scientists. Assignments include characterization of lymphocytes for cell surface and intracellular markers. The associate will be accountable for effectively executing moderate to complex experiments within a defined framework. This position will regularly work with laboratory animals, human tissues and associated biohazard material and waste. Other responsibilities include: * Making detailed observations, analyzing data and interpretation of results. * Preparing technical reports, summaries and quantitative analyses of assigned research projects. Job Requirements Preferably 1 full year related experience in a research laboratory environment. The associate must have working knowledge in science disciplines and with lab equipment. Must be familiar with sterile tissue culture techniques. Education and Experience A BS degree in a life science or related discipline. ]]>

<![CDATA[Process Analyst II The Process Analyst II is responsible for performing data processing, trend analysis, metrics summary, method development, criteria development, etc. in support of production goals and engineering/R&D projects. Essential Duties and Responsibilities * Provide guidance and train data clerks to perform data processing in support of commercial product builds, improvement projects and new products. Monitor product performance. Perform data/trend analysis and metrics summaries to facilitate trouble-shooting and improvement projects. * Assists Manager/Supervisor to conduct on-going projects including Vision Inspection System development, ISOPstat Eight-Channel Calcheck System upgrade, Membrane Thickness Measurement, etc. Develops methods and criteria associated with testing and inspection function. * Works with Manufacturing, R&D, Engineering, QA and RA to review manufacturing procedures, justify current specifications/requirements, and establish new requirements. Supports documentation improvement for better compliance with FDA/ISO regulations. * Functions as a Camstar (MES) application manager; manages on-going work flow configuration and execution including documentation revisions, new product/procedure implementation, work flow execution trouble-shooting, etc. * Assists Manager/Supervisor by overseeing the In-process Testing and Inspection team to support production ramp-up, improvement projects and new product transfer. Requirements * Bachelor's degree (B. A.) from four-year college or university required. * 3 + years related experience and/or training in medical device field required. * Good knowledge and understanding of statistics and trend analysis required. * Experience with statistics analysis software application required. * Must have strong communication, interpersonal and teamwork skills. * Flexible schedule for a possible swing shift. * Programming experience is a plus. ]]>

<![CDATA[Vista, CA based biotech company seeks an experienced and motivated individual to be our new Quality Assurance Coordinator. Please see below for job description. After reading through it thoroughly, if you feel yourself to be the right candidate, please forward your Resume and a cover letter with salary requirements the link above. Please read the ad carefully and submit all of the requested information in order to be in consideration. 1. Position Summary To verify and maintain compliance with established regulatory requirements and company procedures through auditing, training and implementation activities. You will direct and coordinate all documentation to insure compliance with the established quality system. 2. Essential Duties and Responsibilities (other duties may be assigned) • Coordinates if company Quality System Documentation complies with FDA and ISO requirements for medical devices; • Develops, implements and maintains regulatory and quality programs; • Performs internal audits to verify compliance with established company/department procedures; • Prepares Management Review and documents the meeting; • Performs risk analysis during Design and Development Projects; • Trains personnel in company/department policies and procedures; • Interacts with other departments to ensure compliance with company/department procedures; • Interfaces with external regulatory agencies regarding quality systems audits, product registration or other regulatory requirements; • Interfaces with vendors regarding performance of services and products rendered which include calibration results and vendor site audits; • Answers questions and provides guidance in the use of the products as well as the interpretation of results over the telephone regarding OTC products; • Assists with special projects as assigned by management. 3. Knowledge, Skills and Abilities Required to Perform the Job Knowledge of FDA and ISO requirements for medical devices as well as 510(k)/PMA submissions and CE Marking regulations. Computer skills: Microsoft Word, Excel, Access and Power Point. Familiar with QSR auditing, able to interface with all levels of management, good communication skills. The job primarily concerns the adherence to quality but we would like a candidate thatnalso has regulatory experience. 4. Education and/or Experience AA or BA/BS/MS graduate preferred. Industry experience in regulatory affairs, quality assurance and quality system documentation. Internal Auditor Certificate preferred. Engineering degree a plus.a Candidate should have substantial management experience with quality systems in direction, implementation. and execution. 5. Language Skills Ability to read, write, speak and understand the English language. Spanish or other languages a plus.]]>

<![CDATA[Client is looking for pharmaceutical manufacturing technicians for project-based work to occur over the 2+ weeks. Job duties include: <ul><li>Label containers-approximately 400,000 labels must be applied <li>Prepare and clean work area <li>Set up work area for next run </ul> Experience requirement: <ul><li>Documentation is VITAL <li>GMP/FDA experience is a plus <li>Will take high tech assemblers <li>Ability to follow written procedures <li>Comply with safety requirements <li>Must have proven ability to focus on highly repetitive tasks </ul> Shift and Compensation Description: <ul><li>6 or 12 HOUR SHIFTS available (morning and evening shifts available) <li>$12/hr, <li>(for 12 hour shift, 4 hours of structured OT every day you work) <li>Contractors will work Sun, Mon, Tues, Wed one week and Sun, Mon, Tues the second week or Thu, Fri, Sat. one week and Wed, Thu, Fri, Sat the next week. <li>Contract will run for two weeks or until the project is finished. <li>All personal protective equipment and materials will be provided </ul> Application Process:<ul><li>Please send resume to: <a href="mailto:lifescijobs@gmail.com" rel="nofollow">lifescijobs@gmail.com</a> and reference “Pharma Mfg Technician - Temp” in the subject line. <li>Specify what times you would be available to work <li>After receipt of resume, manager will be in touch with you to describe company and job duties in more detail. </ul>]]>

<![CDATA[Research Associate, In Vivo SUMMARY: Seeking a candidate with three or more years of industry related experience using experimental animal systems for the discovery of new chemical entities in the area of nervous system diseases. Candidate should be familiar with a wide variety of live and ex vivo techniques for the study of animal neuroscience. Candidate should have extensive experience in handling rats and mice with chronic dosing using multiple routes of administration. Experience with design, documentation and execution of experiments is required. Independent analysis and presentation of data to the team for in depth discussions and trouble shooting is required. Candidate should be familiar with the design and use of standard operating procedures for performing screening procedures with new chemical entities. The ability and desire to directly participate at the bench as well as in the execution and analysis of experiments is expected. Candidate should have enthusiasm for investigation of novel ways of addressing complex neurobehavioral paradigms for use in drug discovery. Bachelors Degree is required. ESSENTIAL DUTIES AND RESPONSIBILITIES: * Following detailed instructions, conducts in vivo experiments according to study protocols. * Performs drug preparation and administration. * Performs clinical observations on testing animals. * Carries out tissue/blood sample collection and necropsy. * Assists in tissue processing and staining. * Records experimental data and reports findings to appropriate individuals. * Organizes and maintains experimental records. * Performs general laboratory housekeeping and adheres to safety procedures. * Reviews, comprehends and complies with all SOP's and internal guidelines. * Performs other duties as assigned. ]]>

<![CDATA[ Sr. Research Scientist JOB SUMMARY: Highly motivated individual to work with cutting edge technology to discover and study small molecule entities in the area of neurogenesis. Seeking experience with techniques such as tissue sectioning, immunohistochemistry and/or immunofluorescence, light or epifluorescence microscopy, confocal microscopy, and experience working with/handling rodents. Possess enthusiasm for working in a team environment and developing challenging ex vivo, cytological and histological assays. Under minimal supervision, will design, implement and analyze cytological and histological studies. ESSENTIAL DUTIES AND RESPONSIBILITIES: * Designs and executes histological experiments. * Directly participates at the bench and leads and mentors in the planning and execution of experiments. * Successfully investigates novel immunohistochemical methods of addressing complex neuroscientific paradigms for use in drug discovery. * Independently analyzes and presents data to scientific team for in depth discussions and troubleshooting. * Designs and uses standard operating procedures to perform screening procedures with new chemical entities. * Interacts with project leaders and members of project teams to coordinate the histology research efforts for assigned projects. * Analyzes data and interprets results in clear format for presentation during project team meetings and project reviews. * Integrates results into larger project goals and deliverables. * Keeps current with appropriate technical literature and contributes new ideas to advance project work. * Grows technical expertise in the applicable field. * May have overall responsibility for laboratory efficiency, compliance and cleanliness. * May manage and/or supervise other scientific or administrative staff. * Performs other duties as assigned. KNOWLEDGE/SKILLS/ABILITIES REQUIRED: * PhD or equivalent in the biological sciences. * 5+ years related experience. * Extensive experience with in vivo and/or ex vivo neuroscience techniques. * Familiarity with small molecule study and data handling/analysis. * Expert knowledge of scientific principles and concepts. * Familiarity with a wide variety of ex vivo techniques for the study of animal neuroscience, including hippocampal neurogenesis and correlative behavioral effects. * Extensive experience in sectioning, staining and analysis of rat and mouse brain tissue. * Experience with design, documentation and execution of experiments. * Demonstrated success in technical proficiency, scientific creativity, collaboration with others and independent thought. * Excellent record keeping, attention to detail and communication skills. * High level of integrity and self-motivation. * Strong written, verbal, organizational and interpersonal skills. * Thorough knowledge of MS Office products. * Ability to work well with superiors, co-workers and direct reports in a laboratory and office environment. * Ability to change tasks quickly and still maintain attention. * Ability to regularly lift, push, or pull up to 25 pounds.]]>

<![CDATA[Scantibodies Laboratory Inc., one of the largest biotech company in San Diego, is currently seeking an administrative assistant to join its pregnancy test kit department. Summary: Provides administrative support to the department by providing a high level of administrative and clerical support necessary in order to run the department efficiently. Will handle various projects and reports at the same time. Will create and submit changes for documents to Document Control and follow up to completion. Will support PTK Logistics as needed. Essential Duties: Maintain department files Review and maintain all departmental logistics files Initiate and submit documents to Document Control Office tasks: copying, filing Prepare and track document changes and artwork approval routing Prepare, submit, and place domestic shipping orders Provide support for documents, Logistics and PTK planning Job Specifications: High School diploma Good command of English required. Ability to speak, read and write in Spanish a plus. Proficiency in Microsoft Word and Excel required. Must be able to create and maintain reports in Excel Spreadsheets Microsoft Power Point basic knowledge needed Typing skills required Organizational skills required Must be detail oriented Excellent communication skills required Prior general office or administrative experience preferred Must become familiar with and learn how to use company programs (M2M/SmartSolve for example) May need to travel to Mexico, must be able to obtain a US Passport or have other legal documents required for traveling between US/Mexico Benefits include: Medical, dental, 401k with company match, tuition reimbursement & incentive compensation.]]>

<![CDATA[OVERVIEW Ibis Biosciences, Inc. (a subsidiary of Abbott Molecular) has a job opening for a research scientist to join the sample preparation team. This position involves development of nucleic acid isolation protocols for use with a variety of biological specimens in support of our in vitro diagnostic assays. In this position, the scientist will investigate and develop new nucleic acid isolation procedures. PRIMARY FUNCTION: • Conducts sample preparation research utilizing multiple experimental techniques. • Investigates and develops new procedures under the guidance of a research scientist, project coordinator, or R&D Manager. • May act as lead scientist on one project and contributor to other projects. • May supervise technical personnel. • Interacts with other groups and shares information; participates in team activities. EXPERTISE AND PROBLEM SOLVING RESPONSIBILITIES: • Understands and consistently follows documented procedures. • Plans and executes assigned projects; utilizes thorough technical and theoretical understanding of relevant techniques. • Applies quantitative methods: analyzes data, evaluates results, forms conclusions, and provides/implements process or document improvements. • Executes experiments; participates in experimental design. • Utilizes DOE where appropriate. • May assist in the design of experiments for others. • Actively uses the appropriate resources to conduct literature searches. • Applies basic computer skills (includes word processing, spreadsheets, instrumentation-related and Abbott network systems). • Produces reports and documents utilizing advanced writing skills. • Utilizes analytical instruments; trains others in their operation. • Recognizes and resolves technical problems. LEVEL OF ACCOUNTABILITY: Scope: Within project • Contributes to the definition and timely achievement of overall project goals. Ensures activities are consistent with project plan. • Responsible for own Electronic Laboratory Notebook (ELN) documentation, and for the accuracy, quality, and timeliness of experimental results. • Summarizes data and analyzes results, formulates experimental conclusions, and reviews project progress with supervisor. • Actively participates in routine maintenance, lab safety; may assume roles of responsibility, such as training or document control. LEADERSHIP ACTIVITIES: • Prepares and delivers presentations of project results to others; presents data to larger and more diverse audiences. • Teaches processes and problem solving techniques. May lead others in project teams. • Participates in project planning and updates. • Prepares and aligns goals with manager's goals. • Influences decision-making through negotiation, addressing conflict, and by building productive working relationships within a project. INTERPERSONAL SKILLS: • Participate in technology teams. • Develop and maintain internal and external customer contacts to maintain technical knowledge as required to accomplish job objectives. Basic Qualifications: Knowledge of regulations and standards affecting IVDs and Biologics. Ph.D. in a life or physical science; Or B.S. in a life or physical science with 4+ years related lab/industrial experience; Or M.S. with 2+ years relevant experience. Preferred Qualifications: Microbiological or clinical microbiological background; BSL level 2-3 years experience, molecular biology background, nucleic acid isolation experience, nuclic acid chemistry/biochemitry background, analytical chemistry background. US citizenship is preferred. Current government security clearance or the ability to obtain security clearance. If interested, please apply online at <a href="http://track.tmpservice.com/ApplyClick.aspx?id=965225-1810-6993" rel="nofollow">http://track.tmpservice.com/ApplyClick.aspx?id=965225-1810-6993</a>]]>

<![CDATA[AvantGen is an early-stage biotech company that develops novel human antibody-based therapeutics and diagnostics. We are seeking talented, highly motivated and experienced researchers to join our antibody discovery team. Requirements: Postdoctoral/Scientist Position: The candidate should have a Ph.D. degree in biochemistry or closely related field and have extensive experience in antibody expression in yeast (Saccharomyces cerevisiae), strong skills in using analytical tools, such as FPLC and HPLC, and techniques including affinity, ion-exchange, and size exclusion chromatography for protein/antibody purification and characterization. Research Associate Position: The candidate should have a minimum of a B.S. degree in biochemistry, cell biology or closely related field and a minimum of 2-3 years industrial experience in immunoassay development such as ELISA and kinetic assays. Experience in standard protein biochemistry techniques, such as gel electrophoresis, western blotting, protein expression also required. Experience in flow cytometric methods, such as FAC sorting and analysis, is a plus. The ability to work in a focused, methodical and independent fashion within a team to meet project goals and objectives is required, as is the ability to thrive in a fast-paced and challenging work environment. Excellent communication skills (both verbal and technical) and interpersonal skills are required. This positions offer ample opportunity for career development. For consideration, please submit your resume/CV via email to hr@avantgen.com. To learn more about our company, please visit our website: www.avantgen.com ]]>

<![CDATA[Chart a New Direction in Your Life! Genoptix is more than just a company –- we are a team of highly trained professionals working together to optimize outcomes. We specialize in hematologic malignancies, disorders, and subtypes in bone marrow, blood, and lymph nodes, with expertise in the most challenging diagnoses. We also specialize in solid tumor workups using molecular testing. Currently, we have an opening for a: Biopharma Logistics Manager. The BioPharma Logistics Manager is responsible for overseeing all operations related to clinical trial logistics. The position calls for the direct interface with shipping personnel, project management, clients, depots, sites, couriers, and customs brokers. Essential Duties & Responsibilities Note: Other duties may be assigned. · Manage import/export requirements, coordination of clinical samples (blood, bone marrow and tissue blocks) from study sites to testing labs, distribution and inventory management of test kits in accordance with project requirement. · Setup and manage clinical trial supply chain including customs brokers at relevant hubs · Identify and assess risks and developing strategies/solutions to manage them · Provide logistics expertise and guidance to Business Development and other departments within BioPharma Services; serve as Subject Matter Expert on international supply chain best practices, sharing knowledge and training within and across internal teams. · Note potential issues and takes action to prevent their occurrence when possible and escalate when necessary · Communicate effectively and timely with Business Development and external customers as necessary to facilitate integrity of clinical specimens and supply chain; monitor supply of shipping materials required to execute international shipments. · Create Logistics procedures that detail shipping requirements for BioPharma studies including SOPs for kit assembly and QC · Lead design, assembly and QC of specimen collection kits · Prepare shipping documentation; confirm all international import/export documentation requirements prior to dispatch of shipments and verifies accurate documentation · Track inventory/expiration of kits at study sites and incoming shipments; ensure that shipments are not delayed/held by Customs · Keep proper shipping/receiving metrics (i.e. supplies, transit time) · Use Genoptix FLEX system to document sponsor requests & communications Qualifications · At least four years of pharmaceutical or clinical trial experience. · CRO or IVRS experience is a plus. · At least four years of experience in handling imports /export. · Knowledge of clinical trial logistics, including international import/export and customs document requirements. · Excellent knowledge of IATA, DOT and Cold Chain UN-Packaging for shipping and storing requirements and FDA and USDA import requirements. · Working knowledge of DEA regulations and ability to be certified for handling of Controlled Substances. · Demonstrated experience in process improvement and problem solving. · Experience in policy writing. · Excellent computer skills. · Experience with MS office. Education and/or Experience · Bachelor's degree from four-year college or university required. · At least four years of pharmaceutical or clinical trial experience. Genoptix offer a competitive salary package with benefits including vacation and sick pay, extensive insurance coverage, flexible spending accounts, 401(K) match, employee stock purchase plan, tuition reimbursement, and more. Genoptix is more than just a laboratory – we deliver actionable results to improve patient care. For immediate consideration, please apply online via the following link: <a href="http://tbe.taleo.net/NA4/ats/careers/requisition.jsp?org=GENOPTIX&cws=1&rid=635" rel="nofollow">http://tbe.taleo.net/NA4/ats/careers/requisition.jsp?org=GENOPTIX&cws=1&rid=635</a>]]>

<![CDATA[Scantibodies Laboratory Inc., one of the largest Biotech company in San Diego, is currently seeking a Quality Control Inspector I to join the Diagnostic Kit Manufacturing department. Summary: The QC Inspector will conduct inspections of components for diagnostic test kits during the various stages of processing according to approved standards. The QC Inspector interacts with manufacturing personnel to ensure that production demands are met. Such activities ensure compliance with GMP/QSR requirements, ISO standards, customer approved procedures and finished product specifications. Essential Duties: Read, interpret and follow RMSs, SOPs, and other procedures Perform inspections and sampling Ensure proper documentation of inspection activities Ensure proper labeling and segregation of approved and quarantined materials Ensure availability of appropriate, required QC inspection materials and supplies Communicate with and provide essential information to DKM Leads and Supervisor Recognize and segregate non-conforming product and material defects Ensure facility and process compliance with GMP/QSR requirements, ISO standards, approved procedures and product specifications Act as a resource for all employee quality related concerns Maintain a safe, organized, and clean working environment for employees Other related duties as requested Job Specifications: Requires a High School diploma or equivalent Ability to write legibly and record results accurately in appropriate documentation Vision must be correctable to normal Must be able to read and write English fluently Suitable experience performing in-process quality inspections is preferred Benefits include: medical, dental, 401k with company match, tuition reimbursement & incentive compensation.]]>

<![CDATA[A premier supplier of bio-compatible silicone medical devices and components to the medical device, pharmaceutical & biotech industries is seeking a Director of RA/QA to lead Quality System, ISO-13485, FDA, MDD 93/42/EEC, MDD Amendment 2007/47/EC, and Medicare compliance. Applicants should exhibit solid RA/QA knowledge, excellent leadership skills, strong communication skills, and a passion for results. Essential Functions and Basic Duties: • Responsibility as a management representative will include liaison with external parties on matters relating to the quality management system. • Develop and implement internal Quality/Regulatory documentation processes to meet FDA & ISO and other regulatory compliance requirements. • Develop and implement a cross functional internal audit program/team to ensure all regulatory requirements are met. • Lead and provide expert advice in the areas of compliance QSR, ISO13485. • Monitor and report on all regulatory compliance activities within the business units. • Lead assigned due diligence and new business integration activities as required. • Develop QMS initiatives to drive simplification and standardization throughout the organization. • Manage overall coaching, training, development and succession plans for the regulatory and quality assurance teams. Qualifications: • BS in Science or Engineering and Lead Auditor certification or ASQ Professional Certification • 5 years minimum manufacturing background in medical device or pharmaceuticals. • 5 years management experience in dealing with FDA and other regulatory bodies. • Excellent communication skills. • Ability to effectively interface inter-departmentally. • Perseverance in investigating alleged non-compliance. • Effective organizational, technical and problem solving skills. • Computer skills in word processing, spreadsheets, and databases highly desirable. • Proven success with FDA and Notified Body interface. • Understanding of the internal Quality Management System, United States Quality System Regulation (21 CFR 820), the Medical Device Directives, ISO 13485, CAN/CSA–ISO 13485 and all other applicable medical device regulations. • Experience and demonstrated understanding of quality assurance in a medical device manufacturing and sales environment. • Experience with silicone or rubber processing highly advantageous. A competitive salary is offered, relocation package, plus a full range of benefits including medical, dental & vision insurance, basic & supplemental life, long term & short term disability, and 401K currently is 100% vested after 2 years. More importantly, you’ll become a key player at a rapidly growing medical device engineering and manufacturing company. ]]>

<![CDATA[Polymer Lab Operations Technician Campbell Membrane Technologies, Inc. (CMT) is a privately owned company that develops, manufactures, and markets flat-sheet membranes for specialty spiral wound membrane filters. CMT specializes in membrane applications for pharmaceutical, dairy, sweetener, and other large process and wastewater markets by developing novel membranes and servicing these industries in the microfiltration (greater than 0.1 micron filtration) and ultrafiltration (1000 Dalton – 100,000 Dalton) molecular weight cut-off filtration ranges. CMT is in high growth, start-up period and is currently relocating to a new manufacturing and development facility in El Cajon, CA. CMT is looking for an individual with hands-on, small industrial and laboratory interests and aptitude, who functions well in a small company environment. We are seeking a part time Polymer Lab Operations Technician to join our team to do analytical testing, work with filter testing and day to day lab operations at our El Cajon, CA location. Responsibilities include, but are not limited to: 1) Work directly with solvents and polymers to make experimental bench-scale thin-film membranes for industrial separations 2) Run performance tests on experimental and production membranes 3) Run protein, TOC and other analytical methods to determine degrees of separation by films and field filters 4) Test large-scale membrane filters for performance in applications lab 5) Operate production equipment to make large scale thin-film membrane Requirements: 1) BA/BS degree in a science discipline preferably in Chemistry or Biology with a minimum 2 years college chemistry, or equivalent experience 2) Aptitude and interest to perform meticulous analytical laboratory duties 3) Mechanical aptitude. Able to load and unload filters in industrial environment 4) Able to lift 40-50 lbs 5) Good Communication skills (writing, verbal) Please note that this position is a Part Time role. Campbell Membrane Technologies offers a very competitive compensation package. Please apply directly to www.alcockmcfadden.com or send a resume to recruit@alcockmcfadden.com. ]]>

<![CDATA[POSITION SUMMARY: Under the supervision/guidance of our scientists and senior management this part-time position is responsible for researching, documenting, preparing and editing detailed project related documents and company specific procedures. The Technical/Scientific Writer ensures that documents are effectively and clearly written and comply with internal guidelines in terms of content, structure and style. Responsibilities also include critical reviews and edits of other written materials and assistance in quality control of content. ESSENTIAL DUTIES: Will write/review/edit the following documents: Study Protocols/Outlines Study Reports/In-Life Summaries Standard Operating Procedures (SOPs) Other documents as needed REQUIREMENTS: Bachelor'?s degree (BS) with major in life sciences; PhD or MD students preferred Comprehensive knowledge of biological science and statistics Experimental research experience Strong organizational, interpersonal and communication skills including the ability to communicate complex information effectively and accurately Effective writing skills with acute attention to detail to meet timelines without compromising document quality Fluent computer skills with strong knowledge of M/S Office (Word, Excel, PowerPoint, Outlook) Ability to maintain confidentiality of sensitive information ]]>

<![CDATA[To Apply: <a href="http://jobs.ucsd.edu/bulletin/job.aspx?cat=research&sortby=post&jobnum_in=52282" rel="nofollow">http://jobs.ucsd.edu/bulletin/job.aspx?cat=research&sortby=post&jobnum_in=52282</a> Apply By: 9/2/10 DESCRIPTION: Under supervision of senior technical and academic members of the research group, provide analytical, technical, logistic and computer support for a long-term atmospheric chemistry research program studying greenhouse gases and ozone depleting substances in the global and regional atmosphere. Responsibilities include operating and maintaining gas chromatographic and mass spectrometric instrumentation, preparing calibration standards, handling high pressure gases and vacuum systems, processing and quality controlling data, and providing logistic support for local laboratory operations and for a global network of atmospheric measurement stations. ~~Position requires travel domestically and perhaps internationally. QUALIFICATIONS: * Four-year College Degree in a relevant area of Science or Engineering; OR an equivalent combination of training and experience. * Experience and skill working in an analytical laboratory environment, including operating and maintaining analytical instruments. * Ability to work with close attention to detail and perform repetitive tasks meticulously. * Familiarity and experience with handling gases at high pressures and with vacuum and high-vacuum equipment, including safety procedures and regulations. * Proven experience and skill using standard PC software for databases, graphical applications, word processing and e-mail. * Good oral and written communication skills with a command of English and a proven ability to communicate and work effectively with others. Preferred: -Experience with gas chromatography and mass spectroscopy, including digital data acquisition systems. SPECIAL CONDITIONS OF EMPLOYMENT: Must possess a valid license to drive a rental vehicle and a valid passport. ]]>

<![CDATA[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. 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 organized. 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. This position requires fulfilling certain weekend duties. ]]>

<![CDATA[To Apply: <a href="http://jobs.ucsd.edu/bulletin/job.aspx?cat=research&sortby=post&jobnum_in=52268" rel="nofollow">http://jobs.ucsd.edu/bulletin/job.aspx?cat=research&sortby=post&jobnum_in=52268</a> Apply By: 9/1/10 DESCRIPTION: Perform experiments using a variety of standard molecular biology procedures concerning the role of hypoxia and tumorigenesis. Analyze the effect of potential HIF inducers on HIF target gene expression and conduct in vivo and in vitro experiments. Conduct experiments to isolate DNA and RNA from cultured mouse embryonic fibroblasts and astrocytes. Assist in writing papers, manuscripts, journal articles, and proposals for research. Manage laboratory, including providing work direction and training for undergraduate lab assistants, ordering supplies and equipment, serving as safety coordinator and other duties related to laboratory administration. ~~Occasional overtime (evening or weekend) may be required by particular experiments. ~~Must safely handle and store chemicals, biochemicals, hazardous chemicals, biohazardous materials and radioactive materials. QUALIFICATIONS: * Demonstrated strong theoretical knowledge of Anatomy, Physiology, Genetics, General Chemistry and Biochemistry acquired through a combination of extensive study and experience. * Strong experimental background in molecular biology techniques applicable to studies involving mice, embryonic and adult models. Experience in handling and culturing mouse embryonic fibroblasts. * Ability to perform DNA replication including radioactive labeling, immunostaining of fluorescent tagged DNA within nuclei, quantitative immunofluorescence, nuclear isolation, and DNA isolation. * Ability to perform PCR, protein purification, Western blotting and immunoprecipitaion, and gel electrophoresis techniques isolating RNA. * Knowledge of experimental tumorigenesis. Knowledge of in vivo and in vitro tumor growth to analyze growth regulation, vascular density and necrotic regions. * Knowledge of MSDSs, hazard communication, and Injury and Illness Prevention Program safety precautions including appropriate clothing and shoes; safe storage and handling of chemicals and biohazardous materials; and use of protective items such as gloves and goggles. ]]>

<![CDATA[This is a one time research project to locate, identify and find a protocal to eliminate an insect. We have a biting insect in our yard that is NOT a flea. I have never been able to see this insect as the bite shows up a day after we are in the yard and the itch lasts a week. Very itchy. The biting season is from May through September. It is a dirt yard. Truly Nolan Pest was not able to identify or kill it. We are willing to pay $300 to the person (grad student or professional) who can identify this insect and find a protocol to eliminate it permantly and another $50 to apply the protocol. Same person or not. Partial payment upon confirmed identification and protocol and final payment upon application of control and viewing its effectiveness. Please e-mail with your qualifications or background or call 760-436-0069]]>

<![CDATA[Biotech firm in sunny Carlsbad seeks an experienced and motivated individual to be our new Quality Assurance Coordinator. Please see below for job description. After reading through it thoroughly, if you feel yourself to be the right candidate, please forward your RESUME and a BRIEF COVER LETTER with SALARY EXPECTATION via the link above. Please read the ad carefully and submit all of the requested information in order to be considered. NOTE: YOU MUST HAVE PRIOR EXPERIENCE MANAGING QUALITY ASSURANCE. Interviewing starts today! 1. Position Summary To verify and maintain compliance with established regulatory requirements and company procedures through auditing, training and implementation activities. To answer incoming telephone calls and respond to consumer inquiries regarding the company’s Over-The-Counter (OTC) product lines 2. Essential Duties and Responsibilities (other duties may be assigned) • Coordinates if company Quality System Documentation complies with FDA and ISO requirements for medical devices; • Develops, implements and maintains regulatory and quality programs; • Performs internal audits to verify compliance with established company/department procedures; • Prepares Management Review and documents the meeting; • Performs risk analysis during Design and Development Projects; • Trains personnel in company/department policies and procedures; • Interacts with other departments to ensure compliance with company/department procedures; • Interfaces with external regulatory agencies regarding quality systems audits, product registration or other regulatory requirements; • Interfaces with vendors regarding performance of services and products rendered which include calibration results and vendor site audits; • Answers questions and provides guidance in the use of the products as well as the interpretation of results over the telephone regarding OTC products; • Mails replacement products to customers, and assists in resolving customer issues/complaints; • Assists with special projects as assigned by management. 3. Knowledge, Skills and Abilities Required to Perform the Job Knowledge of FDA and ISO requirements for medical devices as well as 510(k)/PMA submissions and CE Marking regulations. Computer skills: Microsoft Word, Excel, Access and Power Point. Familiar with QSR auditing, able to interface with all levels of management, good communication skills. Good phone and customer skills; ability to remain calm when dealing with possible irate/difficult callers; and ability to describe technical information in a clear and comprehensive manner. 4. Education and/or Experience AA or BA/BS/MS graduate preferred. Industry experience in regulatory affairs, quality assurance and quality system documentation. Internal Auditor Certificate preferred. 5. Language Skills Ability to read, write, speak and understand the English language.]]>

<![CDATA[Job Purpose: The Production Chemist is responsible for coordinating and running processes associated with the manufacturing of the customer's product. The Production Chemist will also write procedures, perform validations and investigate any variances as necessary. The ideal candidate should be able to work with minimal instruction. Duties include: * Communicating with customer. * Coordinating the scheduling of job to be performed: -Needed personnel -Equipment and space * Ensuring inventory is available pre-production. * Set-up and formulation of buffers and solutions. * Timely completion of all documentation throughout entire job process. * Verify that personnel follow all applicable regulations and written procedures. Qualifications: Education: Bachelor's Degree in Biology or Chemistry preferred. Minimum of 3-4 years of verifiable college coursework in the sciences or equivalent work experience is required. Experience: Experience within a Quality regulated manufacturing laboratory is desirable or classroom laboratory experience Good documentation and record keeping skills are mandatory. Good organizational and communication skills are required. Word processing skills and Excel knowledge are mandatory. Competitive Compensation and Benefits Package ]]>

<![CDATA[B2B Sales Pros Wanted Seeking career oriented individuals with a track record of success to sell internet marketing solutions to real estate professionals. No order takers please - we are seeking sales professionals that can navigate a short sales cycle and close over the phone. Prior B2B sales and internet marketing experience is a big plus. Select entry-level candidates with exceptional oral and written communication skills and who have the ability to work in a fast paced environment will be considered. Compensation and Benefits Info: <ul> <li>Guaranteed Base Salary <li>Comprehensive Paid Training <li>Uncapped Commissions on all Sales <li>Weekly Sales Bonuses <li>Medical, Dental & Vision Insurance, 401k and Other Benefits <li>Professional Environment <li>Exceptional Room For Career Growth</ul> First year sales consultant typically earn $30,000-$40,000. Mid-level to top producers earn $50,000-$75,000 and higher. These are realistic numbers and not inflated. Hours of Operation 7:30am-3:00pm / Monday-Friday Apply Now & Interview ASAP We are now interviewing professional career seekers with a stable work history in sales. To learn more about this opportunity please email a copy of your resume and you will be contacted with more info and an opportunity to interview. ]]>

<![CDATA[E M ENERGY SYSTEMS, INC. IS SEEKING A CHEMIST TO DO WORK ON ELETRO-MAGNETICS. SEE OUR WEBSITE emenergysystems.com FOR A BRIEF DESCRIPTION.]]>

<![CDATA[Excellent opportunity to join a successful international manufacturing organization (Consumable Products) This is a highly visible position, reporting to the Director – Worldwide Regulatory Affairs and works closely with senior level management across multiple departments. The company offers a friendly work environment and a 9/80 work schedule (every 2nd Friday off!). Objective: This position is responsible for the following as they relate to the organization: a) compilation and dissemination of international product registration packages and related documents, b) Master List of Ingredients (MLI) creation and review, including coordinating with various departments to ensure accuracy of information, c) packaging and literature review, ensuring accuracy, appropriate claims, and regulatory compliance, and d) management of Product Safety Committee. The Regulatory Affairs Manager will uphold the highest standards while maintaining the mission and integrity of the organization. Responsibilities: - Master List of Ingredients (MLI) creation and review - Compilation and dissemination of international product registration packages and related documents - Packaging and literature review - Management of Product Safety Committee - Management of Product Dossiers - Facilitate/disseminate MSDS for all products Requirements: - Bachelor degree - Minimum five years regulatory experience working for a manufacturer of consumable products - Must have excellent analytical, oral and written communication skills, be highly organized, and be able to handle multiple priorities simultaneously. - Must be highly proficient in using Lotus Notes, Adobe Acrobat Professional and Microsoft Office (Word, Excel, Access, PowerPoint). - Must be able to work independently and proactively and have the ability to lead others. - Knowledge of licenses ]]>

<![CDATA[Do you have some university level/practical understanding of horticulture? Are you insanely curious and self driven? Do you wonder why some cultivars respond better to light vs others or what makes lettuce bolt or tomato leaves turn yellow? Are you computer savvy? If so, let's chat. New bio/agri startup is looking for a research assistant to develop plant growth protocols and perform design of experiments in a new kind of hydroponic greenhouse. Part time for now- flex time great for students. Could transition to full time and salary. Send C.V/Resume' and a brief intro paragraph of why you think this is a good fit for you.]]>

<![CDATA[Dexcom, Inc., a leader in continuous glucose monitoring, is headquartered in San Diego, California. Our success is built on innovation, hard work, and on seeing each other’s differences as an advantage. We are committed to developing technologies and products that improve the lives of people with diabetes. Dexcom has ambitious plans to keep learning and growing – and is seeking people who have the same goals for themselves. Dexcom is currently seeking a Manager, Hardware Engineering. Job Summary The incumbent will be responsible for supervising the HW Engineering Department. Person will responsible for budgeting, scheduling, and staffing of the department, as well as contributing to projects at a technical level. Responsibilities (other duties may be assigned) • Responsible for project scheduling. • Managing and mentoring department engineers. • Responsible for completing employee reviews. • Develops department budget. • Contributes to projects at a technical level. Requirements • Bachelor's degree of Electrical Engineering or Computer Engineering from four-year college or university required; Master’s degree or higher preferred. • Must have 15+ years overall experience and 5+ years experience in management. • Must have good interpersonal skills and be able to work well in a team environment. • Excellent communication skills are required. • Must have a strong background in board-level development, and experience in interfacing with Contract Manufacturers. • Solid background in microprocessors, digital and analog design also required. • Prior experience with developing portable wireless devices a plus. • Medical device background a plus. About Dexcom Inc Dexcom Inc. is a publicly traded company listed in the NASDAQ stock exchange. We have been FDA approved and commercially released three generations of continuous glucose monitors. 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. To apply please go to www.dexcom.com/careers. ]]>

<![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/BS) from an accredited four-year college or university in a related field and six months to two years related experience and/or training; or equivalent combination of education and experience. Must have knowledge of basic laboratory procedures. Job Description Summary: Will collect samples from clients and process them according to the specified protocol. Will quantitate and evaluate quality of RNA samples using Agilent BioAnalyzer. Will process samples through Affymetrix or Nimblegen assay protocols. Will provide raw data and quality control results to Core clients. Will be in charge of processing expression profiling assays based on the Affymetrix and Nimblegen array designs. Will process client samples from QC to hybridization on Affymetrix Chips or Nimblegen's spotted Array technology. 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=174" rel="nofollow">http://tbe.taleo.net/NA7/ats/careers/requisition.jsp?org=VETERANS_MEDICAL_RESEARCH_FOUN&cws=1&rid=174</a>]]>

<![CDATA[Immunovative Clnical Research, Inc. (Carlsbad), a wholly-owned subsidiary of Immunovative Therapies, Ltd., (www.immunovative.co.il) an Israeli corporation located in Jerusalem, is seeking a highly motivated Research Associate to join our Carlsbad team. We conduct and manage clinical research studies on an investigational drug product that has living immune cells as the active ingredient. Our Carlsbad facility has a medical clinic staffed with physicians, nurses and medical assistants for administration of the investigational drug per approved protocols in compliance with Good Clinical Practices (GCP). The drug is activated and formulated in a class 10,000 clean room in strict compliance with GMP regulations to prepare for patient administration. We conduct aseptic processing of the drug product, QC and QA procedures and conduct research to optimize and validate the processing, packaging and delivery of the drug. In addition, patient tumor and blood samples are analyzed for immunological response to the drug. This position will have responsibilities in GMP drug processing, quality control, immunological monitoring and R & D. Candidate must work well in a team, be willing to work flexible hours, have good organizational skills, and be capable of following and adhering to written instructions. Qualified individuals will have a BS with minimum 5 years experience or MS with minimum 2 years experience in an immunological laboratory or equivalent with excellent sterile technique, experience in cell culture, microbiology techniques, ELISA, and flow cytometry. Experience with internal cytokine staining, bead array analysis, gram stain, NK assay, tetromere assay, surface marker staining, immunomagnetic bead cell subset purification techniques, and CD3/CD28 T-cell activation beads is preferred. Experience with GMP rules and regulations is desired, but will train. Interested candidates should send cover letter with CV and salary history by email to: thu@immunovative.co.il or by fax to 760-444-9044.]]>

<![CDATA[<img src="http://www.trilinkbiotech.com/gif/welcomesm.png" border="1"> QA Manager: Seeking an individual to manage the Quality Assurance department. BS in science required. A minimum of three (3) years experience in a controlled industrial environment is mandatory. (cGMP/GLP). Excellent writing skills, high degree of organization, exceptional attention to detail and proven managerial skills are necessary. Responsibilities include design, implementation, maintenance, and improvements to the quality systems. These systems include but not limited to documentation system, documentation review procedures, document and process change controls, deviations, CAPA & NCMR systems, materials and lot release process, validations systems, vendor qualification and compliance system and internal and external audits. The ideal candidate must have the ability to communicate to all levels of the business both internal and external. TriLink is a rapidly growing biotech firm in Sorrento Mesa that offers competitive wages and a full benefit package including medical, dental, vision, LTD, and a retirement plan. Qualified applicants submit resume and salary requirements to: hr@trilinkbiotech.com or fax (858) 546-0020 ]]>

<![CDATA[NexBio, Inc. Clinical Operations Associate Location: San Diego, California-San Diego 92121 Posted on: August 20, 2010 Position type: Full time Job Code: NB0137 Required education: Bachelors Degree Area(s) of expertise desired: Clinical Research Description NexBio Inc. (www.nexbio.com) is a fast growing biopharmaceutical company dedicated to create and commercialize novel, broad-spectrum biopharmaceuticals to prevent and treat current and emerging life-threatening human disease. NexBio focuses on the treatment of diseases through distinct host-targeting mechanisms of action. Fludase® (DAS181), a novel broad-spectrum recombinant protein for the prophylaxis and treatment of Influenza-Like Illness caused by all influenza and parainfluenza viruses, as well as pandemic influenza caused by strains such as H1N1 and H5N1, are currently in Phase 2 clinical trial. Sepcidin™, at lead optimization stage, is directed to the treatment of viral hemorrhagic fever caused by viruses such as Ebola, as well as sepsis and septic shock. TOSAP®, a micro particle formulation technology invented at NexBio, is offered as a service and technology licensing business to third parties, as well as a source of internal pipeline development. As the world faces the mounting threats from an influenza pandemic and from other bioterror agents, NexBio's therapeutic programs have enjoyed very generous government funding and high levels of public interest. NexBio is looking for highly motivated, dedicated, and competent individuals to strengthen our team. NexBio is an equal-opportunity employer. The company operates according to the following philosophy: - We focus on important medical problems. - We are dedicated to translating scientific knowledge into clinical therapy for the public good. - We build a team with common goals, solid values, and high competency. - We nurture open communication, personal growth, and professional development. - We believe in work-life balance and offer flexible work schedules. - We strive for cost-effectiveness. Two Clinical Operations Associate position are available immediately. The Clinical Operations Associate is responsible and accountable for supporting the daily Clinical Operations functions for a study or a series of studies within a project. The Clinical Operations Associate applies a working knowledge of GCP and ICH guidelines as well as NexBio Clinical SOPs to support the Clinical Study Manager in the management of the clinical study. The Clinical Operations Associate will work in conjunction with the regional Clinical Research Associates (monitors) to manage and oversee study sites. The Clinical Operations Associate may act as a back up to the Clinical Study Manager. • Assist in the development, collection and collation of site feasibility data • Create and maintain the planned and active site list • Create and maintain study team contact log • Develop site regulatory packages based on the country requirements • Oversee the distribution, collection, review and approval of essential regulatory documents • Responsible for ensuring proper filing and archiving of essential regulatory documents • Assist in the preparation of required regulatory documents for FDA & NIH submission • Assist in the selection of central Institutional Review Board (IRB) • Coordinate the submission, review and approval activities for both local and central IRBs • Assist in the selection of external service provider vendors (e.g., central laboratory, courier companies, etc.) • Coordinate the development of the proposed Investigator Grant • Oversee the distribution, negotiation, execution and tracking of the Clinical Trial Agreement (CTA) and Investigator Grant in collaboration with NexBio legal counsel • Responsible for Investigator grant administration (site payment tracking, check requests and distribution) • Assist in the development of the Clinical Study Reference Manual (SRM), Site Regulatory Binder and Pharmacy Binder • Responsible for site distribution of study specific supplies and study binders • Assist in the development of study specific tools and forms (source document worksheet, study specific logs) • Responsible for tracking and reporting enrollment • Develop and distribute study newsletters • Coordinate, maintain and distribute the frequently asked questions log • Responsible for the development and maintenance of electronic tracking of study documents • Responsible for the reconciliation of the electronic to hard copy Trial Master File • Responsible for the set up and maintenance of the Trial Master File (core and Investigator files) • Assist in the document archiving activity as necessary • Assist in the coordination of all aspects of the Investigator and CRA training meetings including developing agenda, meeting material, coordinating presentations. • Attend and generate meeting minutes for all internal and external Clinical Study team meetings • Assist Clinical Research Associate close out activities (reconciliation of TMF to site regulatory binder) Experience and Qualifications: The requirements listed above are representative of the knowledge, skill and ability required. Working knowledge of cGCP and ICH guidelines applicable to the tasks described above. We seek a focused, self-motivated, creative, independent thinking and dedicated individual to join our highly productive team. This position offers ample opportunity for career development. NexBio offers competitive salary, attractive stock options, and full benefits. Current work authorization in USA is required. Local applicants preferred please. For consideration, send your resume and a concise e-mail cover letter describing your qualifications to hr@nexbio.com. Ref. # NB0137 ]]>

<![CDATA[Scantibodies Laboratory Inc., one of the largest Biotech Company in San Diego, is currently seeking a Senior Chemist IV to join its Cell Culture Department. Summary: To participate in the manufacturing of products according to established GMP, MMPs and SOPs. To maintain a professional atmosphere and ensure that all company policies are complied with. Work with the supervisors of each manufacturing department to help facilitate the efficiency of their production runs. Maintain the physical facilities and equipment of Scantibodies. Assist in the training of technicians and chemists. Effectively communicate current production status to shift supervisors and customer service staff. Job Specifications: BS degree in Chemistry/Biology or related field and at least 5 years comparable experience in diagnostic industry. Benefits include: Medical, Dental, 401k with company match, tuition reimbursement & incentive compensation.]]>

<![CDATA[Scantibodies Laboratory Inc., one of the largest Biotech company in San Diego, is currently seeking a Calibration Specialist I to join its Quality Control Department. Summary: Develop and improve the company-wide calibration and environmental programs. Coordinates, schedule and analyze all aspects of the calibration and environmental monitoring improving efficiency. Provide technical support to personnel regarding calibration and environmental protocols. Provide support for validation activities and with the purchasing of new equipment for new or existing activities, as needed. Comprehend the role that calibration and environmental monitoring has in the laboratory/manufacturing area and its effect on producing high quality products. He/she uses effectively his/her knowledge to reduce the equipment failures of OOS by optimizing the equipment setup and in turn help prevent potential quality risks. Strive to make the job more efficient while maintaining compliance. Follow GMP’s, ISO 9001-13485 (or latest ISO) standards. Supports other departmental duties such as QMR Reports, NCMR processing, validations, and batch record review. Comply and apply ISO 10012, Z540, and ISO 17025 as appropriate. Job Specifications: High School Diploma or equivalent required Must have a minimum of 3 year experience in the calibration of the type of equipment used at SLII and or environmental monitoring or related field Read and follow written and verbal instructions Write clearly and legibly with good verbal communication skills Practice good time management and organizational skills Must be detail oriented and be willing to learn Follow all safety policies at all times Maintain confidentiality at all times Benefits include: Medical, dental, 401k with company match, tuition reimbursement & incentive compensation.]]>

<![CDATA[Scantibodies Laboratory Inc., one of the largest Biotech company in San Diego, is currently seeking a Quality Auditor to join its Quality Control Department. Summary: The QA Auditor position is responsible for planning, organizing, conducting and managing Quality audits of SLI and Supplier processes in the manufacturing of IVD, drug, and biologics products. The person in this position has a strong background in the pharmaceutical industry and will review and recommend audit / compliance related policies / procedures as well as evaluate impending regulations, guidelines and industry standards, and their impact on the Quality Audits for the SLI. This position requires frequent travels to Tecate, Mexico manufacturing site which may include overnight stays. Job Specification: 1. BA/BS in Health/Life Sciences or equivalent work experience. 2. A minimum of 4 years of industry experience in the quality field. 3. A minimum of 2 years experience in the biomedical industry. 4. A minimum of 3 years previous audit experience, both internal and supplier audits required. 5. Certified quality auditor (CQA) or Certified Biomedical Auditor (CBA) or equivalent strongly preferred. 6. Demonstrates a thorough knowledge of cGMP and ISO 13485 regulations and guidelines. 7. Excellent written and oral communication skills and interpersonal skills. 8. Ability to effectively manage multiple projects. Benefits include: Medical, dental, 401k with company match, tuition reimbursement & incentive compensation.]]>

<![CDATA[Scantibodies Laboratory Inc., one of the largest Biotech companies in San Diego is currently looking for a Information Systems Manager to serve as a subject matter expert and provide technical assistance for all IT-related operations. This person must have an ability to conduct customer support duties and recommends necessary IT action pertinent to all aspects of customer support. Will be responsible for maintaining systems configuration as well as resolving IT equipment/software interfaces and interoperability problems. Continually reviewing hardware and software to ensure that it is responsive to user needs, creating and monitoring accounts, network rights, and access to systems and equipment. IS Manager is also responsible for monitoring systems resources, applying the installation and integration of system fixes, updated and enhancements to include performance, capacity, availability, serviceability and recoverability; troubleshooting all aspects of the system, including hardware, software, and communication lines. Essential Duties: Administer network, email, security, disaster recovery and databases Assist users with hardware, software or network problems Manage IS Technicians Research information system purchases Planning and Research of information system purchases Project Management and Documentation Assist with Audio Visual projects and events Telephone and Voicemail Administration Job Specifications: Computer Science degree, Unix, Linux, or Microsoft Certification, or equivalent work experience required. Minimum of five years experience in Network and Server administration and computer repair. Must possess extensive knowledge of Windows XP, Windows Server 2003, Active Directory, Windows Terminal Server, Microsoft SQL Server, Microsoft Exchange, Microsoft Office products such as Word, Excel, Visio and Outlook. Experience with Oracle Database, Wireless Networking, Virtualization, Unix, Linux, Cisco Routers, SAN and NAS Storage, and VLANSs is highly recommended. To be a part of the team you must have the ability to work in a busy work environment with multiple priorities and have the ability to work in a moderate to high stress level. ~Regular Travel to the Tecate Facility is also required. Scantibodies Laboratories offers an innovative work environment along with excellent benefits that Include, Medical, Dental, Vision, paid vacation/sick/holidays, assistance with continuing education and quarterly incentive compensation. visit our website at www.scantibodies.com ]]>

<![CDATA[Young, fast-growing company in inland North County is currently seeking to add more Part-Time Lab support staff to their already dynamic group of individuals. We are seeking only positive, friendly, upbeat individuals that are driven by accuracy in their work and with strong attention to detail. This is not your ordinary lab support job or company. It is imperative that each candidate is able to work in a fast paced environment where multitasking and attention to detail are a must. Lab support staff will be handling specimens and ensure the line is moving at a quick pace without any delays. If you feel you have the all capabilities we are seeking, are ready for a new challenge, and are open to a frequently changing environment, please read additional qualifications and requirements: • High school diploma or GED • Ability to multitask in a fast pace environment • Lab background is a plus • Ability to be on your feet performing rapid/accurate processing of specimens and supporting other lab staff. • Ability to meet expected goals of sorting and processing a large amount of specimen within a specified time limit. • Ability to contribute and be an asset to the company while maintaining a high level of professionalism as well as integrity. • Willing to set goals and strive to be the best team player with current staff •Ability to lift 40 lbs. as job entails working with trays and an industrial dishwasher for lab equipment •Ability to handle some tasks in an area with no air conditioning where the climate may be hot or cold •Ability to work 4 to 5 hours per day Please note that only applicants who meet the above listed requirements and follow all directions will be considered. All applicants interested in interviewing for this position must not be allergic to dogs and enjoy working around them as we do have a dog on company premises. Our company also promotes a smoke free environment. PLEASE, NO STAFFING AGENCIES! Location: Rancho Bernardo Compensation: To be discussed Principals only. Recruiters, please don't contact this job poster. Please, no phone calls about this job! ]]>

<![CDATA[<h2>Architectural Historian (San Diego) - Job #28090</h2> Position Description EBI Consulting is seeking to fill a full-time, Architectural Historian to work remotely from their home office to prepare Section 106 and National Environmental Policy Act (NEPA) reports for projects throughout the San Diego Metro Region. Travel throughout the region is required. Position Requirements Strong technical report writing skills and ability to conduct intensive archival and technical research is a must. Prior working experience in Section 106 regulatory process and direct experience in preparing Section 106 compliance documents is preferred, but not required. Applicants should be able to effectively communicate with EBI’s employees and clients and work as part of a team. Extensive local and regional travel will be required. Education Requirements M.A. required in Historic Preservation, Architectural History, Art History, History or other directly related field. Registration Requirements Candidate must meet the Secretary of the Interior’s Professional Qualifications Standards for Architectural History. Company History EBI Consulting, founded in 1989 to provide management consulting due diligence based on best technology and practices in Environmental Health & Safety. EBI has grown to $40 million in revenues in 2007 and is expected to exceed this in 2010. EBI has built three distinct and diversified businesses working for Real Estate (EB-RE), Telecom (EB-TC), Industrial & Institutional (EB-IIS) clients including the top names in these fields, such as Bank of America, JP Morgan, Morgan Stanley, Prudential, John Hancock, AT&T, Verizon, Sprint Nextel, Bechtel, General Dynamics, EMDSerono, Genzyme, Harvard University, Cambridge Hospital and hundreds more. One key to achieving this growth is to continue to recruit and retain people with exceptional technical and business management experience. We must then capitalize on their expertise by providing improved operating results for EBI's growing and diversified client base and business relationships. EBI Today Business Segments: <ul> <li>Real Estate- Engineering and environmental due diligence services including site assessments and engineering evaluations for real estate investors, mortgage bankers, and investment bankers. Clients include hundreds of most important commercial and investment banking companies and real estate owners and operators nationally. </li> <li>Telecommunications- Engineering and environmental due diligence for wireless carriers and tower companies for collocation and site development. EBI utilizes our diverse team resources, to provide full range of Architecture & Engineering, Radio-Frequency Electromagnetic Energy, and Environmental Health & Safety services. EBI delivers flexible, cost-efficient solutions. Clients include dozens of most important wireless companies and their general contractors such as Bechtel and General Dynamics. </li> <li>Institutional & Industrial Services- Full-service Environmental, Health & Safety and management consulting services assisting Healthcare, Life Sciences, and Manufacturing and Educational clients create business value through best-practices with compliance and permitting, risk management, and enterprise-wise sustainability programs. Clients include dozens of the most important companies and institutions in these growing areas. </li> </ul> The Opportunity EBI Consulting has grown by 30% to 50% in nine of the last twelve years, always profitable and cash positive. This includes two years of $10 million growth (50% & 33%) and one year of $5 million (35%). Similar growth is planned for 2010 and beyond bringing revenues to $50 million by 2013 and $100 million in this decade. Based on the diversity and quality of its client relationships and of its existing and planned management and technical capabilities, EBI Consulting is positioned better than ever to achieve this growth. Plans and Expectations for Future Growth for EBI EBI has implemented an aggressive plan to develop new business lines, acquire new clients, as well as invest in existing lines of business that have potential for significant growth. We work with and for our clients to provide Business Management Consulting to enable them to improve their profitability and marketability by implementing Environmental Health & Safety as well as other improvements. For more information about EBI and open positions please visit our website at www.ebiconsulting.com. What the Successful Candidate Should Anticipate We expect the successful candidate would work with our team to help EBI realize our goals while at the same time, the successful candidate will realize personal, professional and financial growth. Benefits EBI offers competitive compensation, bonus opportunities, group medical & dental insurance, 401k plan with employer contribution, tuition reimbursement, paid vacation, and progressive career opportunities. EOE M/W/D/V Submittal Please submit a resume and cover letter in Word or PDF format via email to <a href="mailto:jobs@ebiconsulting.com" rel="nofollow">jobs@ebiconsulting.com</a>. You must include the following information: <ul> <li>Reference job #, job title and resource </li> <li>Brief summary of past related experience (highlight your experience as it relates to our need & industry) </li> <li>List of your education credentials and professional registrations </li> <li>Salary history </li> </ul> We look forward to hearing from you! ]]>

<![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a Research Associate to work for a leading San Diego biotechnology company. Research Associate Responsibilities: * The successful candidate will be involved in all aspects of the antibody discovery and engineering process. * Responsible for performing standard molecular biology and biochemical techniques including: PCR amplification, cloning, library construction, mutagenesis, sequence analysis, immunoassays, and binding kinetic determinations. * Working collaboratively with other groups to achieve objectives and timelines. Requirements: * Candidates should have a B.S. in biological sciences (immunology, molecular biology, biochemistry, or similar field) with at least 2 years of relevant academic or industrial experience. * Strong skills in molecular biology techniques and/or biochemical assay development are required. * Excellent communication, planning, organizational and record keeping skills (with an attention to detail) are essential. * Highly self-motivated individuals with the ability to thrive in a team-oriented setting in a fast-paced drug discovery environment are desired. Experience in high throughput cloning, phage display or protein screening is a plus. Visit <a href="http://www.biophaseinc.com" rel="nofollow">http://www.biophaseinc.com</a> to view additional opportunities throughout San Diego County!]]>