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<![CDATA[Our client is a leading biotech research company seeking additional personelle for their R&D department. This position requires previous lab and/or industry experience. Job Description: Under supervision, this person will be preparing media plates, buffer solutions, and glasswashing, and completing lab inventory. Prior experience with PCR, protein purification, DNA extraction, and HPLC is required. Knowledge of Microsoft Office and Excel is a must. Requirements: Bachelors of Science with 0-2 years lab/industry experience. For immediate consideration, please contact Brian Riehle at 619-278-3022 and email your resume and salary history to briehle@aerotek.com ]]>

<![CDATA[Volcano Corporation provides rewarding and challenging employment opportunities for those qualified and selected individuals wishing to join us as we develop, market, and manufacture products that improve the overall quality of medical care. Come join Volcano Corporation - a team leading the way! JOB SUMMARY: The Senior Marketing Manger has complete responsibility for developing, recommending, and executing global commercialization strategies for a group of product lines or segments. This includes coordinating and integrating global marketing plans and activities to ensure strategic objectives and product revenue, market share, and gross profit targets are met. This individual will have global upstream and downstream responsibility for Volcano’s sound and light based, high resolution imaging platforms – rotational intravascular ultrasound (IVUS) and recently acquired optical coherence tomography (OCT) – used by physicians to treat patients with vascular and structural heart disease. Within the first year, this individual will have the opportunity to launch multiple “new-to-world” catheter, pullback, and console products that will help Volcano continue to grow over 30% per year. RESPONSIBILITIES: <li> Primary marketing lead on cross-functional product development teams, from project initiation through full market release. This includes performing market research with customers and sales teams, assessing market dynamics and opportunities, collecting competitive intelligence and identifying business risks, creating Marketing Design Input documents, and managing design validation testing. <li> Primary marketing lead for product launches and lifecycle maintenance. This includes promoting products with clear and concise messaging, developing sales forecasts and demand plans, defining pricing and reimbursement strategies, educating and training field sales, handling complaints, and supporting the global sales organization in meeting financial targets. <li> As necessary, performs other duties as required. REQUIREMENTS: EDUCATION: <li>BA/BS (or equivalent work experience), preferably in engineering, life sciences, or marketing <li>MBA or advanced degree preferred KNOWLEDGE AND EXPERIENCE: <li>7+ years experience in a medical device company focused on vascular or structural heart disease <li>5+ years medical marketing experience that may include a combination of brand/product management, market development, market planning/research, marketing communication, sales education/training, or sales <li> International experience is a plus LICENSES AND CERTIFICATIONS: . <li>Additional professional education as appropriate with career level. ADDITIONAL DESIRABLE QUALIFICATIONS: <li>Dynamic, motivated, resourceful individual able to accomplish what is needed and make impactful strategic decisions <li>Interested in joining and thriving within a fast paced organization with significant corporate and individual growth potential SKILLS AND ABILITIES: <li>Superior interpersonal and group communication skills <li>Strong presentation building skills, including the use of various media elements <li>Must be able to build strong relationships with physician Key Opinion Leaders spanning interventional cardiology, interventional radiology, and vascular surgery <li>Must be able to build strong relationships with Volcano marketing/sales personnel and other functional groups within the organization <li>Command of Microsoft Office products including Excel, Outlook, Powerpoint, and Word <li>Prior experience with salesforce.com is a plus PROBLEM SOLVING AND DECISION MAKING: <li>Shows good judgment in all functional areas, including budgeting, priorities and interpersonal relationships PHYSICAL REQUIREMENTS: <li>Ability to hear and speak to employees and outside business associates on the phone and in person <li>Ability to sit for long hours at a time <li>Ability to see the letters and numbers on a personal computer screen and on memos, reports and other documents (near vision) <li>Ability to lift, carry, push and pull up to 50 pounds SUPERVISORY RESPONSIBILITY: None TRAVEL REQUIREMENTS: <li>Moderate to heavy (30 to 50%) domestic and international (Europe, Japan) travel. Interested candidates should send a resume to: jobs@volcanocorp.com and include the reference code in the subject line. Ref code: SMM-283 EEO/AA M/F/V/D ]]>

<![CDATA[Scantibodies Laboratory, Inc., one of the largest Biotech Companies in San Diego is currently looking for a courier with inventory experience for the materials department. Duties: Job Duties will include providing courier/delivery service in support of general production to various locations. Pick up orders, deliver and maintain transactions in the tracking system. Cycle count and inventory of part numbers. Requirements: High School diploma, 1 year general manufacturing background, inventory experience preferred. Valid California Drivers License. Benefits include: Medical, Dental, 401K, tuition reimbursement and incentive compensation. Apply in person at: 9336 Abraham Way, Santee, CA 92071 or via email at hr@scantibodies.com or fax resume to: 619-258-3974. ]]>

<![CDATA[This position will support the Cost Accounting Manager and will have general accounting responsibilities. Monitoring of all job order activities and inventory, assisting in month-end close. Maintain cost system in Made2Manage. Track and analyze labor efficiencies. Analyze material, labor & overhead variances including PPV. Bachelor's degree in Accounting and 2 years accounting experience in a manufacturing environment. Maquiladora experience and bi-lingual in Spanish preferred. Apply in person at Scantibodies Laboratory, Inc. at 9336 Abraham Way, Santee CA 92071 or online at www.scantibodies.com or via email at hr@scantibodies.com or via fax at 619-258-3974. ]]>

<![CDATA[Job Description: Carlsbad office has an opening for an entry level Quality Control Technician who is detailed oriented and conscientious. Responsibilities: Quality Control operations supporting the process of manufacturing, testing, labeling, and shipping high quality products. Attention to detail and multi-tasking are a MUST. Some Duties: Maintenance, calibration and troubleshooting testing equipment, fill checking and line clearance, testing and releasing raw materials and final products, documentation. Qualifications: *BS/BA in Biology, Chemistry or equivalent education and experience. *0-2 years of experience in cGMP manufacturing or laboratory environment. *Experience in Clinical Diagnostic Manufacturing a plus. *Experience in an FDA/ISO regulated industry is a plus. *Able to prioritize, math skills, and good organizational skills needed. *Computer Skills: MS Office (Word & Excel). *Quick learner, self starter, and strong ability to multi-task. ]]>

<![CDATA[Alfama, an innovative European-American early-stage drug development company, seeks a senior scientist with deep managerial skills, superior drug development track-record, and the capacity for bold leadership and team-work, to join and lead our fast-paced international development team. Your responsibilities will include rapid and efficient delivery of several INDs from the company’s portfolio of opportunities, and hands-on management of several centers of internal and external biologists and chemists located in the U.S. and in Europe. Substantial experience in pre-clinical drug development is required. A background in medicinal chemistry would be ideal. You must be willing to relocate to Boston, Lisbon, and/or spend significant travel time in European and U.S. company locations. Information about Alfama is available at <a href="http://www.alfama.com.pt/." rel="nofollow">http://www.alfama.com.pt/.</a> Additional information is available from Alfama’s UK subsidiary at <a href="http://hemocorm.com/." rel="nofollow">http://hemocorm.com/.</a> Please send a detailed resume in confidence by email.]]>

<![CDATA[Company Overview: Hollis-Eden Pharmaceuticals, Inc. is developing a proprietary new class of compounds that are metabolites or synthetic analogs of adrenal steroid hormones. These compounds, designed to restore the biological activity of cellular signaling pathways disrupted by disease and aging, have been demonstrated in humans to possess several properties with potential therapeutic benefit. We are dedicated to reaching our goal of a renaissance in health care through the collaborative effort of our people. Please learn more about us at <a href="http://www.holliseden.com" rel="nofollow">http://www.holliseden.com</a> Job Description: This is a great Opportunity to join our closely-knit Clinical Development Team with responsibility for the successful execution of domestic and international clinical trials, including: -Design, plan, and implement clinical trials, -Monitor clinical trials conducted according to Good Clinical Practices -Assist in writing clinical study protocols -Track and review regulatory documents -Assist in field monitoring and data management activities as well as coordinate activities with contract laboratories -Manage drug supply, write and maintain clinical SOP's and assist with data queries and data review -Participate in CRO selection, site selection and Investigator's Meetings Requirements: A BS degree in the Life Sciences with 2-10 years monitoring experience as a clinical research professional in the biopharmaceutical industry. Earlier stage industry experience is helpful. Background should include a solid working knowledge of regulatory applications to clinical research, including knowledge of ICH Good Clinical Practices. Further, it is important to be able to clearly articulate complex concepts and ideas to your peers and throughout the organization. The successful detail-oriented candidate will have excellent interpersonal skills and be effective working in a collegial team environment. Contact: Please e-mail your resume/cv with your name, job title and code 'CRA2-CL' in the subject line to jobs@holliseden.com. Please attach your resume as a Word document. EOE, Diversity Focused, and Drug Free Workplace Employer. A background check and pre-employment drug screening will be required. ]]>

<![CDATA[Anaphore, Inc. is a platform-based drug development company. The company is developing novel protein therapeutics to address significant medical needs in autoimmune and inflammatory diseases and oncology. Anaphore, Inc. is located in the La Jolla, North Torrey Pines area. We are seeking two Research Associates to work in a fast-paced team environment. The successful candidates will have either a BS with at least 3 years of experience or an MS with 1-2 years of experience in a biotechnology laboratory setting. Candidates are expected to be skilled in molecular biological and tissue culture techniques. Individuals will be capable of independently planning and carrying out basic cloning stratagems, and of competently performing bacterial and mammalian cell culture, ELISA, and transfection protocols with minimal supervision. Candidates will be capable of and expected to perform data analysis and presentation using Excel, Powerpoint, and Word, and will keep an up-to-date notebook on all experiments performed. Experience with phage display, reporter assays, FACS and/or Biacore are a plus. Please send CV to hr@anaphoreinc.com ]]>

<![CDATA[Product Manager Seeking a Product Manager to hold a position with the up most quality and attention to detail who can bring products from conception to commercialization. This individual must have had experience in a Medical Device, BioMedical or Diagnostic company as a Product Manager. Listed below are more details: Responsibilities: • Participate in overall product strategy, research and development requirements, and manufacturing coordination for new and emerging products. • Coordinate technical product development, estimate potential profit, and release to production. • Manage day-to-day progress of product line(s). Provides technical expertise and training to other departments in support of product development as well as ongoing product sales and support. • Conduct marketing analysis to develop product definitions. • Collaborates with a wide variety of functional areas such as sales, engineering, marketing, manufacturing, and operations to develop and provide product definitions responsive to customer needs and market opportunities. Requirements: • Bachelor's degree (B. A.) from four-year college or university and four plus years related product management experience in medical device, pharmaceutical or a high technology environment. • Must be able to perform each essential duty satisfactorily. • Must be able to travel domestically and abroad, must have passport, as well as be able to travel 20-30 % of the time]]>

<![CDATA[Outstanding pharmaceutical company seeks candidate to work closely with Clinical trial manager to plan and project adequate drug supply. Will order and track shipments, and maintain clinical trial inventory. Will ensure proper collection and storage of clinical samples, and ensure maintenance of clinical trial master files for assigned studies. Will apply knowledge of clinical trial process and regulations (FDA, ICH, GCP regulations, SOPs and guidelines) to ensure appropriate study conduct. Will ensure regulatory compliance for all assigned tasks/projects.]]>

<![CDATA[Are you an energetic, flexible, multi-talented production chemist who thrives in a fast paced, high-demand environment? Are you looking for significant personal and professional growth opprotunities? Can you multi-task and manage varied projects? Our production chemists perform ranging from analytical and functional testing of antibodies, protein purification and conjugation process to maintaining and analyzing lot histories for trends and discrepancies. They think of ways to improve manufacturing process while maintaining high quality standards. They write SOPs for new production procedures and reviewing and editing existing SOPs to reflect changes in procedures. If you have a BS in biochemistry, chemistry or related discipline and 1-2 years relevant experience working with column chromatography (affinity purification, ion-exchange and gel filtration), gel electrophoresis (SDS-PAGE, IEF gel required) and are up for a challenge, contact us today to be considered for this dynamic postion. Apply now for this once in a lifetime opportunity! Apply and submit resume to go www. biolegend.com ]]>

<![CDATA[Advanced BioHealing (ABH) is a specialty biotechnology company focused on the development and marketing of cell-based and tissue-engineered products. We are a privately held company with two approved products: Dermagraft® and TransCyte®. Our development pipeline also includes a next-generation bioengineered wound therapy for which two Investigational Device Exemption (IDE) applications have been approved by the Food and Drug Administration (FDA). We currently have an opening for a Process Development Associate at our La Jolla, CA manufacturing facility. Job Title: Process Development Associate II Department: Process Development Reports To: Manager, Process Development SUMMARY This position is responsible for assisting in several biology/engineering projects to improve current process systems and/or to bring new products to market. The PD Associate II must be able to demonstrate the understanding and use of scientific theory that crosses research techniques. The PD Associate II demonstrates creativity in troubleshooting and developing new solutions or improving upon existing components, processes and equipment by performing experimental studies, prototyping, and scale-up activities; supporting manufacturing needs; and creating relevant documentation for cGMP compliance. The PD Associate II completes projects with increased independence and self-reliance, and demonstrates teamwork and initiative in the interactions with their co-workers. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. % of Time Job Task 40% Designing, writing and executing, documenting, and analyzing experiments/ protocols and associated data; designing, building and refining prototypes; developing parameters for equipment and process validation. 20% Creating supporting documentation for cGMPs including standard operating procedures, batch records, forms, and specifications; creating supporting documentation for validations and qualification tests. 15% Maintaining lab supplies and materials necessary for performing experiments/protocols. Coordinates preventative maintenance, calibrations, and cleaning as required. 15% Planning and communicating the status, requirements and decision points of current projects with internal department manager(s). 10% Searching for appropriate vendors, materials and components to complete assigned projects. SUPERVISORY RESPONSIBILITIES Position has no FTE supervisory responsibilities; however, may provide guidance and instruction for other Associates or interns, as required. QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. • Experience/training in cellular/molecular biology, cell culture, and aseptic technique. • Ability to summarize and present scientific information, in both written and oral formats. • Familiarity with routine laboratory equipment (e.g. centrifuge, analytical balance, pH meter). • Design of experiments and statistical analysis and interpretation of results. • Organizational skills and ability to complete assignments/tasks with minimal supervision. • Computer skills and familiarity with Microsoft Word, Excel, PowerPoint, graphing software and statistical analysis software. • Experience/familiarity with FDA-regulated industries and products. EDUCATION and/or EXPERIENCE B.S. degree in chemical engineering, bioengineering, or related discipline with minimum of 5 years of professional experience. M.S. degree in chemical engineering, bioengineering, or related discipline with minimum of 2 years of professional experience. LANGUAGE SKILLS Ability to read, analyze, and interpret professional journals, technical procedures, or governmental regulations. Ability to write technical reports, business correspondence, and scientific procedures. Ability to communicate effectively in oral form to present information and respond to questions from vendors, managers, and other functional areas within the company. MATHEMATICAL SKILLS Ability to perform basic scientific/laboratory calculations, statistical analysis, and an understanding of significant digits and scientific notation. Ability to use statistical and graphing software to present experimental findings. REASONING ABILITY Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form. Ability to establish hypothesis-driven experimental designs and follow scientific principles in analyzing and interpreting data. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Routine laboratory benchwork will be required (including standing, repetitive motions, and lifting up to 50 lbs). Ability to use appropriate personal safety protective equipment and work with various chemicals and hazardous materials. Must be willing to work in an clean room environment, including following gowning requirements. Please review our website at www.advancedbiohealing.com for more company information. We offer a competitive benefits & compensation package! All qualified resumes should be submitted directly to careers@advancedbiohealing.com We are an Equal Opportunity Employer. ]]>

<![CDATA[La Jolla Institute for Allergy & Immunology (www.liai.org) Responsible for research and development in collaboration with others. Makes detailed observations, analyzes data and interprets results. Works on problems of diverse scope in which analysis of situation or data requires evaluation of identifiable factors. Exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions. Normally receives no instructions on routine work, general instructions on new assignments. Requires a BA/BS Degree, some previous laboratory experience is required. Experience with molecular biology, tissue culture and/or small animal work is highly desired]]>

<![CDATA[Qualifications Summary: Seeking Ph.D. or M.D., from an accredited college or university. Must be detail oriented; exercise good judgment skills; ability to collect and analyze data with precision; must be able to communicate effectively and manage projects. Must be able to work with and make scientific progress with cell culture, enzyme assays, and other molecular biology techniques and small animal models. Previous supervisory and trainer experience. Job Description Summary: Will perform a wide variety of laboratory techniques which includes animal handling (tissue harvesting) and usage of radioisotopes and toxic chemicals; will supervise and guide research technicians in their current research projects and will train Post Doctoral Fellows and Research Assistants; will conduct scientific literature reviews, independently pursue new techniques, and assist in manuscript and other grant-related preparatory work. May perform additional duties as required. How to Apply: Please submit a cover letter, resume, application form, release form, confidentiality agreement, confidential data sheet and the contact details of three references. Please reference job number RT-RS-0372-08. Application and forms can be found at our website www.vmrf.org under Careers. ONLY SIGNED AND DATED FORMS WILL BE ACCEPTED. Veterans Medical Research Foundation Human Resources 3350 La Jolla Village Drive (151A) San Diego, CA 92161 Fax: 858.642.3081 Email: jobs@vmrf.org PLEASE REFERENCE JOB# RT-RS-0372-08 ]]>

<![CDATA[Requirements: • Applies knowledge of clinical trial process and regulations (FDA, ICH, GCP regulations, SOPs and guidelines) to ensure appropriate study conduct. • Effective written and verbal communication skills. Provides information in a useful manner • Ability to scope out length and difficulty of tasks and projects; can adjust for issues and roadblocks, measure performance against goals, evaluates results • Proven record of successful completion of tasks with some supervision; includes appropriate prioritization and follow-up of multiple tasks and high level of accuracy. • Ability to identify and solve problems independently. Seeks guidance appropriately. .• Collaborates effectively with Clinical Project Managers, study teams, cross-functional team members, and external partners. ]]>

<![CDATA[• Are you an environmental scientist (biology, air, archaeology) with 5-10 years of experience who is looking for an opportunity to move into management? • Can you envision yourself getting to know clients who need your group’s services, building relationships with them and writing winning proposals that bring projects to your group? • Would you enjoy working with and learning from corporate operations management? Then we have the job you’ve been looking for! Chambers Group Inc, an environmental consulting firm located in Southern California (www.chambersgroupinc.com), has an immediate need for an EXPERIENCED ENVIRONMENTAL SCIENTIST in our San Diego office. The position reports to the Vice President Operations. We need an experienced professional who is good technically, has worked in San Diego, and is looking for an opportunity to step up to a leadership position. This key person will lead staff, develop business, and manage projects and will be part of the corporate bonus profit-sharing program. The successful candidate will have 5+ years of progressively responsible experience in environmental consulting or environmental regulation, and a degree in one of the environmental sciences. A graduate degree is preferred. Exemplary experience will be considered in lieu of advanced degrees The right candidate will also demonstrate initiative, project management skills, strong verbal and written communication skills, field skills and knowledge of ecology, conservation biology and restoration, and problem-solving skills and creativity. Chambers offers competitive salaries, a comprehensive health plan including medical dental, vision, long-term care, and fitness, and performance-based bonus plans. We are proud of our history of nearly 30 years solely in the practice of good environmental science. Our mission is to protect the environment by assuring that our clients are in complete and defensible compliance with all environmental regulations. Send resumes and salary history to cbryan@chambersgroupinc.com. EEO Employer. ]]>

<![CDATA[JOB TITLE: Quality Control Technician POSITION SUMMARY: To perform quality control procedures to ensure product specifications are met. DUTIES AND RESPONSIBILITES: Fill checking and line clearance Testing final products Releasing final products Checking labels Checking shipping documents QC Scheduling Maintenance, calibration and troubleshooting testing equipment ADDITIONAL DUTIES AND RESPONSIBILITES: Investigate and resolve quality problems. Perform and enforce Good Manufacturing Practices. MINIMUM QUALIFICATIONS: BS/BA in Biology or Chemistry or equivalent education and experience. Experience with Microsoft Office. Good organizational skills. Multi-tasking. Good work ethic Detail oreiented PREFERED QUALIFICATIONS: 1+ years of experience in a cGMP manufacturing and laboratory environment. Experience with Clinical Analyzers ]]>

<![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a Process Chemist to work for a leading San Diego biotechnology company. Associate Process Group Chemist The Associate Process Group Chemist, in accordance with forecasted requirements and assignment, participate in the Chemistry Manufacturing department via: -Manufacture products within QSR and ISO regulations -Review/reconcile documents and work orders -Support assigned projects with supervision -Support departmental troubleshooting and process improvement teams -Participate in product transfers -May write/revise documentation with supervision -May train lab technicians -Work with supervisor and Planners to develop weekly schedule -Display improving working knowledge of business processes as they relate to manufacturing -Maintain daily adherence to Production goals relating to MUV/LUV, labor utilization, work order closure, and schedule adherence Skills/Experience/Education -BA/BS in biology or chemistry -GMP experience preferred -Manufacturing experience preferred -Knowledge of basic reagent formulations/basic chemistry -ELISA-based assay experience is a plus -Chromatography experience is a plus -Protein purification experience is a plus ]]>

<![CDATA[Profil Institute for Clinical Research, Inc., a private research institute located in Chula Vista, CA. is currently seeking additional highly motivated Research Nurses to support its growing volume of clinical trial activities. At Profil we are focused on early-phase investigations of potential new treatments for diabetes and other metabolic diseases. The key responsibilities are • Have a clear understanding of the ongoing protocols and study-related clinical procedures; • Providing care for subjects enrolled in clinical trials; • Starting intravenous catheter lines; • Blood draws for pharmacokinetics and pharmacodynamics • Study drug administration under appropriate supervision of MD • Assessment and proper documentation of any possible adverse event occurring to the subjects during the in-house period of the studies • Perform other study-related clinical procedures and patient assessments according to the study protocol Successful candidates should have a proven track record in successfully working in a highly regulated environment. The candidates should thrive for excellence and regularly meet and beat expectations. Profil is growing rapidly offering multiple opportunities for career advancement as well as competitive compensation and outstanding benefits to its employees. Minimum Qualifications: Valid California LVN or RN license California certification for intravenous therapy / blood withdrawal Experience in medical/pharmacological research field Interested applicants should submit their cover letter and resume / CV via email to this ad. Qualified candidates will be contacted.]]>

<![CDATA[Profil Institute for Clinical Research, Inc., a private research institute based in Chula Vista, CA, is seeking additional highly motivated Research Assistants to support its growing volume of clinical trial activities. At Profil we are focused on early-phase investigations of potential new treatments for diabetes and other metabolic diseases. The key responsibilities are • after successfully completing a training program at Profil, perform automated glucose clamp procedures – a unique and technically highly demanding process to measure glucose levels in a patient; • providing care under appropriate supervision for subjects enrolled in clinical trials; • perform study-related clinical procedures according to the study protocol; • observe and record data related to patient safety and study procedures; • ensure that all study data are recorded accurately and completely; • assist nursing staff and Clinical Project Managers with study procedures and patient management as directed; perform screening procedures in the enrollment process of subjects in compliance with specific protocol requirements; • prepare, operate, and maintain study specific equipment and supplies Successful candidates have a proven track record and high interest in working in a technically demanding environment. The candidates should thrive for excellence and regularly meet and beat expectations. Profil is growing rapidly offering multiple opportunities for career advancement as well as competitive compensation and outstanding benefits to its employees. Requirements: Willingness to work evenings, nights and weekends on a regular basis (increase pay-rate based on shift differential is applicable) Bi-lingual in English and Spanish a huge plus BA/BS in the life sciences with extensive laboratory experience (e.g. biochemistry) - OR - Medical Associate / EMT / Corpsman, or equivalent with a minimum of 2 yrs experience Interested applicants should reply via email with their cover letter and resume / CV by replying to this ad. No faxes or phone calls please. Qualified candidates will be contacted. ]]>

<![CDATA[Junior and Senior Level Chemists CalciMedica, Inc., a biotech company based in La Jolla, has immediate openings for full-time BS/MS and PhD Synthetic Organic Chemists. CalciMedica is focused on the discovery and development of small molecule inhibitors of Ca2+-release activated Ca2+ channels (CRAC channels) for the treatment of autoimmune and inflammatory disorders. Candidates should have a successful track record of multistep synthesis that has lead to biologically active molecules. An ability to independently solve synthetic problems and build an SAR within a chemical series is also highly desirable. In addition, the candidates should be able to use the latest database, drug discovery and literature search software. Applicants with a positive attitude and a strong desire to advance compounds to the clinical stage are encouraged to apply. CalciMedica is an equal opportunity employer offering a competitive compensation and benefits package. All applicants should be US citizens or eligible to work in US companies without sponsorship. Please submit resume and cover letter to the email address below: CalciMedica, Inc. E mail: jobs11@calcimedica.com ]]>

<![CDATA[Description: Experience in developing, optimizing, and performing solid-phase immunoassays desirable. Familiarity with lateral flow assays and particle conjugations essential. Primary Responsibilities: The applicant is expected to primarily develop, optimize, validate and transfer to Manufacturing lateral flow tests for detecting and measuring analytes. The applicant will also need to be flexible and adaptive to other R&D projects as assigned. General Responsibilities: The successful applicant should expect to have experience in the use, optimization, and preparation of gold-labeled antibodies, capture antibodies and antigens, and hapten-protein carriers. The applicant will be expected to perform rigorous method validations and data analysis/write-up/submissions. General support duties will include preparation and monitoring the supply of common laboratory, reagents, and buffers. Requirements: BA, BS, or MS in biochemistry or chemistry with 8 years experience or PhD with 3 years experience. The ideal applicant should possess at least 6 years of general solid-phase immunoassay test kit production and development experience (with particular emphasis on lateral flow devices and methods). Requires a self-starter with strong organizational skills and the ability to plan and work to a schedule on multiple simultaneous projects. Proficiency with PC-based applications (MS Word and Excel) and technical writing skills are required. Antibody purification, ELISA, chromatography, and electrophoresis skills are a strong plus. ]]>

<![CDATA[Tandem Labs, a leading contract research organization, provides bioanalytical services, immunoanalytical expertise, and mass spectrometry-based pharmacokinetics and pharmacodynamics in support of new drug discovery and development R&D for the pharmaceutical and biotech industries. We are seeking for scientists to work in a dynamic discovery based quantitative and qualitative laboratory. The position is in our New England facility located at Woburn, Massachusetts. The actual job title, position, and salary will be commensurate with the candidate’s relevant experience. If you are looking for working in a small, dynamic and rapidly growing laboratory environment, but in a larger company where your colleagues become your friends and there is simple a good opportunity to learn and progress, send us your resume. POSITION DESCRIPTION Position Title: Associate Scientist / Research Scientist in Bioanalytical Field Department: Tandem Labs New England Reports To: Group Leader Work Schedule: Monday-Friday. Occasional weekends as determined by workload or staffing needs. Job Requirements BS or MS in life Sciences or the equivalent experience At least two year’s laboratory experience in bioanalytical field; more experience will be compensated appropriately. Skilled in laboratory work include but not limit to pipette, centrifuge, incubator, evaporation devices, balances, pH meter, understand and hands-on experience on Mass Spectrometers is preferred. Able to perform data processing functions in Watson or other LIMS system Proficient in Windows, Excel, and Word, Access, Sigma Plot Attention to details Contact xin.zhang@tandemlabs.com (781) 404-2930 ]]>

<![CDATA[Certified Clinical Research Coordinator position ***DO NOT APPLY UNLESS YOU HAVE EXPERIENCE IN CONDUCTING RESEARCH IN THE PHARMACEUTICAL INDUSTRY**** Excell Research 3998 Vista Way, Suite 100 Oceanside, CA 92056 Position Summary: Conducting and coordinating clinical investigational studies for psychiatric medications Essential Functions: • Coordinate and perform all phases of clinical study projects according to FDA regulations and guidelines and in compliance with Good Clinical Practice • Communicate with and meet with study sponsors and their representatives to discuss the conduct of the study and review study data • Attend investigator meetings • Work with hospital staff to educate them on study protocols and ensure appropriate patient care • Maintain complete and accurate source documents and CRFs • Assist with preparation, submission, filing and maintenance of study-related regulatory documents, and interface with IRB’s • Maintain working knowledge of the specifics and amendments of all assigned study protocols • Assist in recruiting study subjects utilizing various media such as radio, newspaper, internet, and presentations • Perform preliminary screening of patients by telephone screen or chart review to determine eligibility • Schedule appointments, organize materials to be used during study visits, and ensure that all required test and rating scales are completed for each study visit. • Dispense study drug to patients and maintain a log for drug accountability • All other administrative support functions as needed, including general filing, data entry, correspondence, etc. Hours: Monday - Friday, 9:00 a.m. – 6:00 p.m., occasional weekend or other hours required; travel to investigator meetings approximately 4 times a year Qualifications: Clinical Research Coordinator certification; BA/BS degree, or related education in a science or medical related-area including Medical Assistants and LVN’s; at least 2 years experience as a research coordinator working in the pharmaceutical industry clinical setting – ACADEMIC RESEARCH DOES NOT QUALIFY - preferably in CNS research; excellent English communication skills; computer skills (MSWord, Excel, email, online eCRFs); general office skills (filing, faxing, phone work, etc.); attention to detail; strong organizational & time management skills; ability to be flexible, work independently, and take initiative where appropriate. Organization Description: We are a small, dynamic clinical research site, with significant growth expected in the next year. We offer a friendly work environment, and we truly value and reward initiative and creativity in our efforts to build our company. We are creating a team of professionals united in our goals of providing the best possible patient care, conducting the highest quality research, and having fun while doing it. We specialize in clinical trials for a variety of psychiatric disorders, including Phase II-IV studies, and conduct both inpatient and outpatient trials. All staff work very closely with the UCSD trained physicians. This is a great opportunity to join a team of dedicated young women physicians building a first-class psychiatric research organization. Competitive wages based on training and experience, 15 days of paid time off, and paid holidays How to Apply: Please submit cover letter and resumé by email or fax: Carmalee Worsley Excell Research Fax: 760-758-2022 excell@excellresearch.com ]]>

<![CDATA[Stem Cell Scientist sought for long term consultation services in Tijuana's premier hospital within 3 miles of the border. Excellent compensation for 1-2 days of service with transportation provided. Send curriculum vitae and telephone number to John Bancroft at johnbancroftjr@gmail.com]]>

<![CDATA[Associate Process Group Chemist Job Description: This position will be responsible to perform all essential functions related to the antibody protein purification and conjugation process. Other duties include performing analytical and functional testing of antibodies, completing batch records, maintaining and analyzing lot histories for trends and discrepancies, and performing analytical instrument maintenance and troubleshooting. This person may also write SOPs for new production procedures and review and edit existing SOPs to reflect changes in procedures. 20% of the position is glass wash/general lab support. A BS in Biochemistry, Chemistry or related discipline and 1-5 years relevant experience (in industry or academic) working with column chromatography (affinity purification, ion-exchange and gel filtration), gel electrophoresis (SDS-PAGE, IEF gel required). Strong organizational, documentation, and communication skills essential. Candidates must be a self-starter, highly motivated, and dependable. Candidates must also have problem solving, analytical, and quantitative skills and able to work independently and effectively in a team environment. ]]>

<![CDATA[CERTIFIED CLINICAL LABORATORY SPECIALIST (CLS, MLT, MT, RN) We are seeking a California Certified Laboratory Scientist (CLS), California Certified Registered Nurse (RN), California Certified Medical Technician (MT) or California Certified Medical Laboratory Technician (MLT) for a position with a global biotech firm. In this role, you will work at a plasma donor site and will be responsible for following the lab's procedures for specimen handling and processing and test analysis. In this role, the Clinical Laboratory Specialist will: * Maintain records that demonstrate proficiency testing samples are properly tested in the same manner as patient samples * Document all quality control activities including instrument and procedural calibrations and maintenance * Follow the lab's established corrective action policies and procedures whenever test systems are not within the lab's acceptable performance levels * Identify problems that may adversely affect test performance or the reporting of test results * Document all corrective actions taken when the test systems deviate from the lab's established performance specifications The qualified Clinical Laboratory Specialist will possess: * Current California Certification as a Laboratory Scientist (CLS), Registered Nurse (RN), Medical Technician (MT) or Medical Laboratory Technician (MLT) * Minimum of 3 months documented laboratory training in each specialty in which the individual performs high complexity testing For immediate and confidential consideration, please email your resume to info@simplybiotech.com or call 858.487.0507. More information can be found at www.simplybiotech.com. EOE]]>

<![CDATA[Commercialize antibodies for immune system proteins, including Toll-like receptors, dendritic and CD Markers. Includes developing and carrying-out testing protocols, collaborating with company’s co-workers abroad and outside scientists, producing collateral product support material as well as providing technical support of commercialized antibodies. Position is ideal for a scientist who wants both bench and program management experience in an industry setting. Position is based in San Diego, California. Requirements: Scientific and technical expertise in immunology including flow cytometry, western blot and tissue culture. PhD with 1-5 years experience. Excellent written and oral communication skills. Publication record in Toll-like receptor biology strongly preferred. Benefits include health and dental insurance, paid vacation, and a retirement plan. See www.Imgenex.com for additional company information. Imgenex is an international, progressive biotechnology company that develops and manufactures antibodies and other research tools for the Life Sciences market. Imgenex is recognized as a leader in immunology, apoptosis, and cancer research using a pathway analysis approach. ]]>

<![CDATA[Aquatic Adventures educates urban youth about science, the ocean and nature through tuition-free programs, creating the next generation of scientific and environmental leaders. Our vision is threefold: • A scientific community that reflects the diversity of our society. • A society in which urban children and youth are empowered to reach their goals. • A world in which people from diverse communities have an understanding of the sciences, a personal connection to nature and a commitment to steward the environment. BAHÍA is an intensive, after-school and summer program that provides underserved high school students with classroom, lab and field-based marine science education and research experience. The program takes place at Hoover High School, the Aquatic Adventures lab, and various field sites in San Diego; and the Vermillion Sea Field Station in Bahía de los Angeles in Baja California, Mexico. While in Bahía de los Angeles, students work alongside Mexican and U.S. scientists to conduct scientific and conservation based research on the Sea of Cortez. Students gain scientific expertise, increasing both self-efficacy and skills toward a successful future. For more information please visit our website at <a href="http://aquaticadventures.org/BAHIA.html" rel="nofollow">http://aquaticadventures.org/BAHIA.html</a> Overview • Contribute to the success and well-being of a diverse group of students from underserved communities • Aid in the facilitation of classroom and lab marine science lessons • Supervise students during various activities • Support students in conducting scientific field research • Lead exciting outdoor field trips both in San Diego and on the Sea of Cortez (i.e. tide pooling, wetland exploration, snorkeling) • Prepare students for presentations in Bahía de los Angeles and San Diego to exhibit their contribution to science, conservation, and the community of Bahía de los Angeles • Make contributions to group living (i.e. cleaning, coordinating meals) • Work collaboratively with a team of staff to continually enhance program Requirements • Experience teaching or mentoring • Passionate toward the natural environment • Interest in both science and education • Dedicated to the concept of promoting equal opportunity for underrepresented students • Ability to complete rigorous work in a team environment • Prompt and dependable • Ability to swim • Ability to lift and perform physical labor • Successfully pass state fingerprinting check (live-scan) • Ability to provide own transportation during San Diego portions Preferred skills • Conversational Spanish • CPR/First Aid and/or advanced life saving certifications • Snorkeling skills POSITIONS: Currently we have 3 different Directed Research Leader positions. Please note that some positions may require additional responsibilities to be discussed during interview Directed Research Leader 1: Testing methods to reduce incidental capture of sea turtles Overview • Lead 6-8 students in a scientific research project • Develop and facilitate activities in San Diego to prepare students for upcoming field research • The Directed Research Leader will be guided by and have access to a science advisor and lead scientist Requirements • Field research experience • Knowledge of marine habitats, flora, and fauna • Ability to communicate scientific concepts to youth • Working towards or completion of a graduate degree highly preferred Directed Research Leader 2: Community structure and habitat connectivity in wetlands Overview • Lead 6-8 students in a scientific research project • Develop and facilitate activities in San Diego to prepare students for upcoming field research • The Directed Research Leader will be guided by and have access to a science advisor and lead scientist Requirements • Field research experience • Knowledge of marine habitats, flora, and fauna • Ability to communicate scientific concepts to youth • Working towards or completion of a graduate degree highly preferred Directed Research Leader 3: Studying land and sea habitat connectivity & trophic structure in the islands of the Sea of Cortez Overview • Lead 6-8 students in a scientific research project • Develop and facilitate activities in San Diego to prepare students for upcoming field research • The Directed Research Leader will be guided by and have access to a science advisor and lead scientist Requirements • Field research experience • Knowledge of marine habitats, flora, and fauna • Ability to communicate scientific concepts to youth • Working towards or completion of a graduate degree highly preferred OTHER INFORMATION Position Commitment • March 5th (4:00-7:30pm) Staff meeting • March 25th -28th Team training in Baja California, Mexico • June 3rd Staff training • June 14th- 20th Preparation in Bahía de los Angeles, Mexico • June 20th - July 26th Work in Bahía de los Angeles, Mexico • July 30th- August 18th Presentation preparation & continued education in San Diego Training Includes • Overview of teaching techniques and curriculum • Water and field safety training • Student management and diversity training • Professional development is provided throughout the term of the position through interaction with scientists, field experiences, etc. Compensation • A stipend dependent on experience. • All costs of travel will be covered. All living expenses are covered during the study abroad portion by the organization. To apply submit resume with 2 to 3 references to Jamie Weed, Office Manager Aquatic Adventures jamieweed@aquaticadventures.org]]>

<![CDATA[PROVEN Scietific Practice is currently recruiting for a Flow Cytometry Operator to work with our client, 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 biofuels that will substitute for conventional gasoline, diesel, and jet fuel. The successful candidate will have 2+ years of sorting experience using high-speed sorters. Problem solving and trouble-shooting flow cytometry experiments; upkeep and maintenance of flow cytometers. Data analysis of flow cytometry experiments. Requires a Bachelor’s degree or Master’s degree in biomedical (or related field), with a minimum of 3+ years of applicable industry experience. The candidate MUST be a team player with strong organizational skills, and written/verbal communication skills. ]]>

<![CDATA[“The Power to Look Deeper” Awarded the 2008 Grand Prize at the local Workplace Excellence Awards, Gen-Probe is a respected biotech employer of choice in San Diego and a global leader in the research, development, manufacturing and marketing of nucleic acid probe-based products used for the diagnosis of human diseases and for screening of donated human blood. We offer a state-of-the-art facility in a prime location with world-class benefits. We’re currently looking for team members who have “The Power to Look Deeper” in developing the best products, technologies and service. “The Power to Shape Your Future” We are seeking a Process Development Associate I-III, who will help maintain cGMP conditions in our Pilot Plant laboratory and assist with the development of processes for transfer to Manufacturing. This position involves manufacturing bulk solutions and filling material to be frozen or lyophilized to make sure R&D receives reagents for testing. DESCRIPTION OF POSITION RESPONSIBILITIES: ·Produces development, pilot and production materials per written instructions. ·Assists with execution of process validation of new and existing manufacturing processes. ·Troubleshoots manufacturing process problems. ·Stocks and maintains the laboratory supplies. ·Keeps accurate records and documentation. ·Completes laboratory work and associated paperwork by assigned completion dates. ·Produces notebook materials per written instructions. ·Completes ERP transactions. ·Works with Purchasing to purchase equipment to pre-determined specifications. ·Works in cross-functional teams ensuring goals are achieved according to schedule. RELATED BUSINESS/TECHNICAL SKILLS, KNOWLEDGE, ABILITIES: ·Working knowledge of GMP/GLP. ·Aseptic techniques knowledge preferred. ·SAP and/or Livelink experience is a plus. ·Good understanding of validation aspects. EDUCATION AND EXPERIENCE REQUIREMENTS: ·BA/BS and minimum 2 yrs of experience. ·Prior Manufacturing/Laboratory experience is required. Gen-Probe offers a dynamic and innovative work environment along with excellent benefits that include sponsored medical/dental/vision benefits, stock options (NASDAQ:GPRO), bonus potential, 401(k) w/company match, paid vacation/sick time /holidays, assistance with continuing education, on-site fitness center, and our own Waterfall Café. We invite you to view our Career Video! <a href="http://www.view-career-video.com/videos/genprobe/" rel="nofollow">http://www.view-career-video.com/videos/genprobe/</a> Please apply online by visiting: <a href="http://www.gen-probe.jobs" rel="nofollow">http://www.gen-probe.jobs</a> Gen-Probe is an Equal Opportunity Employer. All applicants will be given consideration regardless of race, sex, age, color, national origin, ancestry, medical condition, marital status, sexual orientation, citizenship status, religion, handicap status or veteran status. ]]>

<![CDATA[“The Power to Look Deeper” Awarded the 2008 Grand Prize at the local Workplace Excellence Awards, Gen-Probe is a respected biotech employer of choice in San Diego and a global leader in the research, development, manufacturing and marketing of nucleic acid probe-based products used for the diagnosis of human diseases and for screening of donated human blood. We offer a state-of-the-art facility in a prime location with world-class benefits. We’re currently looking for team members who have “The Power to Look Deeper” in developing the best products, technologies and service. “The Power to Shape Your Future” We are seeking an Oligonucleotide Process Development Chemist I who will be responsible for synthesis, purification and analytical characterization of oligos for use in diagnostic assays. This entry-level role requires a degree in Chemistry or Biochemistry (or related) and some knowledge of DNA, peptides, HPLC, and mass spectroscopy. Role will require 80% bench work. DESCRIPTION OF POSITION RESPONSIBILITIES: ·Independently produces note book, Development, Pilot and production materials per written directions. ·Troubleshoots simple manufacturing process problems. ·Assists in the development of manufacturing processes for transfer to Manufacturing. ·Assists with execution of process validation of new and existing manufacturing processes. ·Assists with simple Failure Investigations. ·Creates development documents and originates simple CCRs ·Analyze development and process data with help. RELATED BUSINESS/TECHNICAL SKILLS, KNOWLEDGE, ABILITIES: ·Working knowledge of GMP/GLP. ·Strong math skills. ·Basic CCR skills. ·Working knowledge of oligo synthesis, purification, diafiltration processes helpful. ·Working knowledge of analytical techniques helpful. EDUCATION AND EXPERIENCE REQUIREMENTS: ·BS degree or equivalent in Chemistry or Biochemistry with 0-2 years experience ·Training in organic, physical and analytical chemistry preferred with some chemistry lab training required. ·Some working knowledge of DNA, peptides, HPLC, mass spectroscopy, etc preferred. Gen-Probe offers a dynamic and innovative work environment along with excellent benefits that include sponsored medical/dental/vision benefits, stock options (NASDAQ:GPRO), bonus potential, 401(k) w/company match, paid vacation/sick time /holidays, assistance with continuing education, on-site fitness center, and our own Waterfall Café. We invite you to view our Career Video! <a href="http://www.view-career-video.com/videos/genprobe/" rel="nofollow">http://www.view-career-video.com/videos/genprobe/</a> Please apply online by visiting: <a href="http://www.gen-probe.jobs" rel="nofollow">http://www.gen-probe.jobs</a> Gen-Probe is an Equal Opportunity Employer. All applicants will be given consideration regardless of race, sex, age, color, national origin, ancestry, medical condition, marital status, sexual orientation, citizenship status, religion, handicap status or veteran status. ]]>

<![CDATA[EDAW Inc, a world leader in landscape architecture, planning, and environmental services has an immediate opening for a technical editor to support our San Diego office. Duties: The successful candidate will be responsible for editing, condensing, formatting, and proofreading environmental documents, proposals, marketing publications, and correspondence. Editing includes verifying style, format, spelling, consistency, and grammar. Skill Requirements: Candidate must have excellent written and communication skills, ability to work independently as well as in multidisciplinary teams, and proficiency in Microsoft Word. Education Requirements: Bachelor’s degree in English, journalism, or related field and 2 years’ editing experience. Please <a href="https://jobs.brassring.com/1033/ASP/TG/cim_jobdetail.asp?jobId=162132&type=search&JobReqLang=1&recordstart=1&JobSiteId=5022&partnerid=20052&siteid=5022&codes=IN-MSTR" target="_blank" rel="nofollow">apply online</a>. For additional information about EDAW Inc., please visit our website at <a href="http://www.edaw.com" target="_blank" rel="nofollow">www.edaw.com</a>. EDAW is an Equal Opportunity/Affirmative Action M/F/V/D <a target="_blank" rel="nofollow">Please apply online</a> Please apply online <a href="https://sjobs.brassring.com/1033/asp/tg/cim_home.asp?partnerid=20052&siteid=5022" rel="nofollow">https://sjobs.brassring.com/1033/asp/tg/cim_home.asp?partnerid=20052&siteid=5022</a> ]]>

<![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a Flow Cytometry Operator to work for our client in Scottsdale, AZ. Flow Cytometry Operator Job Description We are searching for a highly motivated individual with a strong interest in the clinical application of advanced genomics to set up and operate a Beckton-Dickenson Influx 208s flow cytometer. This individual will participate in the day-to-day activities of a research laboratory and the Flow Cytometry Facility. The primary focus of this position will be processing and analyzing patient tumor samples for high definition genomic analyses. Responsibilities will include daily operation of the flow instrument and assisting in the design of novel translational research projects. The operator will also contribute to ongoing assay development and novel applications of flow cytometry and high definiton genomics to the study and treatment of human cancer. The operator will also be responsible for routine maintenance of instruments, including troubleshooting and repair of electronics, fluids, lasers, and computer components. Duties will also include working with equipment field service engineers, ensuring compliance with relevant maintenance contracts, and assisting with budgets, billing statements and balances accounts. -Day to day processing and analyzing patient tumor samples for high definition genomic analysis. -Daily calibration, operation and maintenance of equipment. -Assay development and optimization of novel applications of flow cytometry. -Writing procedures, documentation and tracking of samples, maintaining compliance with applicable regulatory requirements. Job Requirements Bachelor's or advanced degree in the life sciences or related discipline. The successful candidate will hold a bachelor's or advanced degree in a biological or clinical-related science, and a minimum of 3 years of experience in Fluorescence Activated Cell Sorting. A genuine interest in cancer biology and its translation to patient care is essential. Must be able to perform troubleshooting, maintenance and basic repair on electronics, fluids, lasers, and computer components. Must be able to work closely with field service engineers. In addition to daily operation of established procedures, must be able to assist in the design, development and documentation of new approaches to the application of flow cytometry and its translation to patient care. Must be proficient in the use of computers and general office software in addition to technical application and analysis software relating to laboratory equipment. ]]>

<![CDATA[EDAW Inc, a world leader in landscape architecture, planning and environmental services has an immediate opening for a Public Participation Coordinator to support our San Diego office. Part-time or full-time. Duties: Coordinate public participation and outreach programs for diversity of project types, based on strategy including project characteristics, community compositions, governance organizations, and political issues. Helps conduct and facilitate community workshops, charrettes, advisory committees, focus groups, and other types of community meetings. Assists with survey instrument preparation and implementation. Conducts media outreach, stakeholder coordination and relationship-building. Presents to and coordinates with government officials. Creates content for and supervises production of newsletters, fact sheets, workshop materials, workshop/meeting summaries, and other types of project materials. Assists with project management of small to medium projects, including budget management, ensuring deadlines are met, client management, staff coordination and management, and delivery of the final product. Provides additional support to ensure smooth execution of projects. Participates collaboratively on multi-disciplinary teams. Skill Requirements: Generally requires three to five years of related experience. Public speaking, strong attention to detail, and excellent organizational skills. Strong verbal and written communication skills. Spanish speaking and writing capabilities highly desirable. Certification by International Association of Public Participation or in conflict resolution highly desirable but not required. Education Requirements: Bachelor’s degree in Public Administration, Journalism, Public Affairs, Geography, Planning, Environmental Studies or similar discipline; Master’s degree preferred. > Please <a href="https://jobs.brassring.com/1033/ASP/TG/cim_jobdetail.asp?jobId=162132&type=search&JobReqLang=1&recordstart=1&JobSiteId=5022&partnerid=20052&siteid=5022&codes=IN-MSTR" target="_blank" rel="nofollow">apply online</a>. For additional information about EDAW Inc., please visit our website at <a href="http://www.edaw.com" target="_blank" rel="nofollow">www.edaw.com</a>. EDAW is an Equal Opportunity/Affirmative Action M/F/V/D <a target="_blank" rel="nofollow">Please apply online</a> Please apply online <a href="https://sjobs.brassring.com/1033/asp/tg/cim_home.asp?partnerid=20052&siteid=5022" rel="nofollow">https://sjobs.brassring.com/1033/asp/tg/cim_home.asp?partnerid=20052&siteid=5022</a> ]]>

<![CDATA[The new High Tech High campus in Chula Vista has an immediate opening for a 10th grade integrated Math/Chemistry teacher. If interested in this position, please send a resume and cover letter to the reply-to email address. Launched in September 2000 by an industry and educator coalition the HTH schools are small, project-based learning environments that connect students to the adult world through meaningful work and internships. There is no test to get into HTH schools; students who live in San Diego County or anywhere in California may apply, and admissions is done by blind lottery, resulting in an ethnically and economically diverse student body. Curriculum Teams of teachers engage 50-80 students in interesting and challenging, interdisciplinary, project-based work. Students present their work for feedback from classmates, parents, and community experts. All students do an internship and complete a senior project based on their interests. Results With five graduating classes thus far, 99% of our schools’ graduates have gone on to college. Approximately 50% of students are the first in their family to go to college. Please Note: Due to the high volume of resumes that we receive, email is the preferred method of contact for employment opportunities. If we are interested in having you in for an interview, we will contact you. Please understand that we will get many, many applications for every position we have available. We may not get in touch with you unless you appear to be a very strong candidate with a strong cover letter. Effective cover letters in the past have included information about the candidate's background, his/her teaching philosophy, and why the candidate is interested in teaching at a High Tech High school in particular. It is also a good idea to have researched our school (<a href="http://www.hightechhigh.org" rel="nofollow">http://www.hightechhigh.org</a>) before writing the letter. You can also apply for this or any position open at any of our High Tech High schools by visiting our employment website at <a href="http://www.hightechhigh.org/employment.php." rel="nofollow">http://www.hightechhigh.org/employment.php</a> If applying for the current 10th grade math/chemistry position at HTHCV through this site, please make sure to make note of that in your cover letter. ]]>

<![CDATA[Amazing Opportunity to join a leading Biotech company. We are currently searching for a Clinical Affairs/Regulatory Affairs Specialist II for our site in the San Diego Area. We are looking for candidates that come with a strong background in Clinical Research & Regulatory Experience. Candidates should have a strong background working in Medical Device and with the FDA & 501k Submissions. Please read details below and apply if interested. Resumes are being reviewed immediately and candidates that qualify will be contacted ASAP. Thank you! Position:Clinical Affairs/Regulatory Affairs Specialist II Location: San Diego CA Area Position Purpose: • Assist in all activities related to maintaining compliance with requirement of FDA 21 CFR 820, CMDR SOR 98-292, IVDD EN 9879/EC, ISO 13495:2003, International Medical Device Regulations, and USDA / EC 1774 Import / Export regulations. • Oversee all clinical activities related to one or more clinical trials and performing or managing daily in-house operations associated with the trials. This position should be able to independently handle various clinical study assignments. Position Responsibilities: 1. Research, prepare, and update clinical protocols, instructions for use, informed consents, reports of prior investigations, bibliography, case report forms, clinical trial reports, and other study-related documents in consultation with the cross-functional project team, investigators, data management and FDA. 2. Responsible for coordination/execution of all operational aspects of clinical studies, including study start-up, follow up, study closure activities. Provide Clinical / Regulatory representation during audits. 3. May perform monitoring and auditing at participating sites to ensure compliance with the Investigational Plan and appropriate regulations, guidelines, and policies. 4. Conduct ongoing review of adverse event information. Compile and update adverse event logs. May interface with Regulatory agencies, as appropriate. 5. Conduct/supervise training of investigators, site staff, and internal clinical staff. Conduct/supervise site initiation activities. Set-up and maintain (or supervise) accurate study status and accountability logs. 6. Review data listings and tables. Educate internal/external data management on the clinical context of these documents and provide oversight of data reconciliation. 7. Evaluate clinical data/information, write, and revise annual, interim, and final reports and clinical sections of Regulatory submissions. 8. May organize investigator conferences to review findings and advise on study direction, as needed. 9. May organize investigator conferences to review findings and advise on study direction, as needed. 10. Act as both the Regulatory and Clinical resource for New Product Development teams, assuring that project scheduling can be accurately compiled factoring in necessary clinical studies and Regulatory applications/approvals. 11. Write domestic and international regulatory submissions, to include Design Dossiers for CE marking and technical files. 12. Monitor regulations on a global basis. 13. Maintain Regulatory Registrations and licenses. Knowledge/Skills/Experience (KSEs): 1. Minimum BS in a scientific discipline. Advanced degree preferred. 2. Clinical Research 2 - 5 years, in device, biotech, pharma, or CRO setting. Experience managing clinical trials from protocol development to final report. 3. A minimum of 2-5 years of Regulatory experience in Class I - III medical devices. 4. Knowledge of principles of clinical research study design. 5. Strong knowledge of Good Clinical Practice (GCP) and Regulatory compliance guidelines and regulations for clinical trials. 6. General experience in medical device manufacturing, Regulatory requirements / submissions, and worldwide experience in medical devices from the Regulatory and clinical perspectives. 7. Strong knowledge in FDA 21 CFR 820, CMDR SOR 98-292, IVDD EN 9879/EC, ISO 13495:2003, International Medical Device Regulations. 8. Knowledgeable in USDA / EC 1774 Import / Export regulations. 9. Strong motivator/communicator in a compact clinical team working with aggressive timelines. 10. Good communication/negotiation skills with clinical investigators and academic thought leaders; highly professional demeanor. 11. Advanced written, oral, and interpersonal communication skills including proficient knowledge of medical terminology. 12. Strong Computer skills (MS Office products, word processing, spreadsheets, etc.). 13. Ability to multi-task. Strong prioritization and organizational skills. 14. Strong problem solving skills. Compensation: Based on Experience Email Contact: tara_merrow@millipore.com ]]>

<![CDATA[A growing Biopharmaceutical company is looking for a Sr. Manager, Document Management Systems to join the team! The Senior Manager will be responsible for the application administration of the document management systems (EDMS), managing the project documentation, managing hard copy paper Clinical and Regulatory records to support Document Control SOPs as well as continuing the development and use of the system. The ideal candidate will possess excellent organizational skills and strong attention to detail. We are looking for a strategic thinker and a huge team player. This is an exciting opportunity with a dynamic and growing team! Responsibilities will include the following: -Responsible for the application administration of the EDMS as well as the development and maintenance of EDMS procedures, training, validation and system documentation. -Responsible for all aspects of document management including (non-GXP and some GXP) electronic and hardcopy records for drug development. -Ensure facile, yet secured and controlled, access to internal documentation for Clinical, Nonclinical, Chemistry, Manufacturing and Controls (CMC), and RA/QA. -Responsible for the development and implementation of new and existing EDMS capability and potential to meet the needs of the organization and corporate objectives. -Develop and execute Document Control standard operating procedures and guidelines. -Responsible for the creation and maintenance of electronic signature (eSign) procedures and implementation. -In conjunction with Quality Assurance, and Information Technology, develop, execute, and maintain the Cadence Document Archiving Plan. -Lead or assist in the development and implementation of computer system and software validation policies, procedures, practices and templates as needed. -Responsible for supporting inspections by providing accurate documents in a timely manner. -Provide guidance and direction to direct report(s) and/or other junior personnel. Requirements: -Must have 6-10 years experience in the pharmaceutical or biotech industry, including 4-6 years document management systems experience coupled with a BA/BS degree. -Must have previous managerial experience. -Strong knowledge of cGMPs, ISO standards and quality systems. -Experience with internal/external auditing programs. -Familiarity with GXP CFR Part 11 regulations. -Proficient in MS Office (Word, Excel, Access, PowerPoint) and Visio. -Experience with eCTD/marketing application submission. -Certified Quality Auditor credentials, IT experience and experience with a leading multidisciplinary team including development of project plans is preferred. ]]>

<![CDATA[Manages the purchasing, planning, scheduling, and coordination of products from production build into finished goods. Manages the material flow and distribution of raw and finished goods materials to internal and external customers. Qualified candidate must have exp in ivd diagnostics industry, specifically worked with reagents, chemicals and ISO 13485. BS/BA Degree and 3+ years supervisory or management exp in a biotechnology manufacturing organization. 8 years exp in a Planning/Materials role. ERP software exp req'd. APICS preferred.]]>

<![CDATA[Fantastic opportunity for someone in college or just completing college in a science field who has no applicable experience!!!!!!! This is an entry level lab aide position - we will train the skills necessary to perform the job. Eligible candidates must have a POSITIVE attitude, a willingness to learn, and the ability to multi-task in a team environment. Primary duties involve separating of specimens and preparing batches of specimens for our confirmatory departments. Must have a strong attention to detail and be able to organize work flow. Additional duties may include setting up columns, performing extractions, spotting plates, reading results from plates, interpreting data, loading specimens onto GC/MS machines, pipetting, make calculations for reagent preparations and dilutions, other general lab duties. Work schedule: Full time MONDAY-FRIDAY 2P-11P. (no weekends) This is not a temporary or seasonal position. Benefits included with full time position (health, dental, 401k). A successful drug screen will be expected of all applicants. Please, only serious applicants. ]]>

<![CDATA[ The key functions of the Technical Service Specialist include: Providing world-class, professional technical and clinical support of company's diagnostic products for customers via phone and e-mail; training of employees; providing advice and guidance regarding compliance standards and clinical interpretation of results. The Technical Service Specialist requires the following: BS in Medical Technology, Nursing or related field required. Must be computer literate and possess outstanding verbal and written communication skills. Theoretical and practical experience with immunoassays, experience troubleshooting and solving technical problems, familiarity with diagnostics industry, and at least two years related experience (at least one year providing customer support) preferred. Clinical Experience a plus. Must be flexible to work weekday nights/ weekend nights as necessary for phone coverage (on call). May have a liaisonary role and need to work closely with other cross functional departments across the company. Occasional travel may be required. ]]>

<![CDATA[Love Research? Come join the ABM team doing cutting edge research developing wireless, portable EEG systems and medical devices! We are looking for a Full Time Senior Research Associate/Assistant Project Manager. Job requirements: 1) Clinical and Non-Clinical Human studies supervision- our ideal candidate will have executed experimental research projects, preferably with human population. Experience with regulatory processes (IRB and/or ALACC), experimental design, planning and execution of research studies are all helpful. This position will be responsible for working with our technicians and research associates to coordinate subject recruitment, data collection, data management and processing using our patented wireless EEG systems and proprietary software acquisition and analysis programs. 2) Project planning/development and execution: our ideal candidate will have evaluated experimental research projects and either assisted with or independently developed project planning, including meeting regulatory requirements, scheduling of tasks and data collection periods, and ensuring that projects are meeting milestones and deadlines for reporting purposes. 3) Software quality assurance: this position will require learning our proprietary software programs and providing quality assurance support to ensure proper validation of all programming occurs in a timely manner. This will require regular communication with our sister company that provides all programming, developing requirements and specifications, etc. 4) Collaborate with project managers and directors to manage and supervise technicians as needed. Provide mentoring/training for technicians and new hires. For the right person, you will become an integral part of a vibrant, growing medical device/biotechnology company. You may take on primary leadership roles in clinical regulatory areas, software regulatory areas, clinical research, product development, etc. This is not your typical research associate position! Excellent opportunities for advancement are available. Required Skills: Intellectual curiosity and interest in improving people’s lives, excellent problem solving skills, experience with OFFICE suite of products, attention to detail, clerical and organization skills, interest in stretching yourself to learn new skills, excellent work ethic. Minimum Education: Bachelor’s degree (preferably in neuroscience, psychology, biology, bioengineering or related fields), and 1 yr of experience in an experimental based research environment. Optional skills: Past supervisory experience, Clinical research experience, in addition, any software quality systems experience, mechanical engineering or basic electrical skills are a great bonus. Pay will be $40K-$45K year, commensurate with experience and opportunities for merit raises within 3-6 months for exceptional candidates. If this sounds like the opportunity for you, please contact us with your resume (include SR RA position in the subject line): HR@b-alert.com ]]>

<![CDATA[ “The Power to Look Deeper” Gen-Probe is a global leader in research, development & manufacturing of nucleic acid diagnostics that offers exciting opportunities in the advancement of human healthcare. Recognized as one of San Diego’s leading biotech companies, we offer a state-of-the-art facility in a prime location with world-class benefits. We’re currently looking for team members who have “The Power to Look Deeper” in developing the best products, technologies and service. “The Power to Shape Your Future” Looking to advance your career in the biotech Industry? Here at Gen-Probe we are working on developing diagnostics that can save lives through early detection of many current and future health threats. Would you like to contribute to this important work? If so, we want to hear from you! We are currently seeking a Development Supervisor with the following qualifications: DESCRIPTION OF POSITION RESPONSIBILITIES: <ul><li>Designs and executes complex experiments. <li>Assists in developing strategies to ensure achievement of strategic objectives. <li>Monitors completion of tasks and projects. <li>Supervises laboratory work to assure completion in accordance with established safety procedures. <li>Writes and reviews data summaries for regulatory submissions <li>Writes reports covering data and non-data project topics. <li>Collaborate with outside groups on project-related issues or studies.</ul> RELATED BUSINESS/TECHNICAL SKILLS, KNOWLEDGE, ABILITIES: <ul><li>Knowledge of molecular biology, biochemistry, chemistry or related disciplines <li>Good understanding of Gen-Probe technology and nucleic acid amplification <li>Understanding of Scientific Method, experimental design and statistical analysis <li>Ability to design both standard and factorial experiments appropriate for research. <li>Ability to troubleshoot and solve technical issues <li>Ability to present data to groups both internally and externally <li>Sound Technical writing. Ability to write and edit technical documents such as technical reports <li>Ability to interact across multiple departments <li>Ability to work in and/or lead small teams <li>May participate as a team member on a project or program.</ul> EDUCATION AND EXPERIENCE REQUIREMENTS: <ul><li>PhD/MS in Biochemistry, Chemistry, Molecular Biology or equivalent in engineering and a minimum of 2-5 years related experience or BS degree with addition with additional experience. <li>Industrial experience in product development would be an advantage, especially experience working under a design control system.</ul> Gen-Probe offers a dynamic and innovative work environment along with excellent benefits that include sponsored medical/dental/vision benefits, stock options (NASDAQ:GPRO), bonus potential, 401(k) w/company match, paid vacation/sick time /holidays, assistance with continuing education, on-site fitness center, and our own Waterfall Café. We invite you to view our Career Video! <a href="http://www.view-career-video.com/videos/genprobe/" rel="nofollow">http://www.view-career-video.com/videos/genprobe/</a> Gen-Probe is an Equal Opportunity Employer. All applicants will be given consideration regardless of race, sex, age, color, national origin, ancestry, medical condition, marital status, sexual orientation, citizenship status, religion, handicap status or veteran status. To Apply for this position, please <a href="http://genprobe.contacthr.com/12237774" rel="nofollow">CLICK HERE</a> ]]>

<![CDATA[Our client is seeking resourceful knowledge-developers and problem-solvers with strong technical and communication skills to support our engineering, risk management and loss prevention needs. The positions below require individuals with a Ph.D. degree to plan and conduct both basic and applied research related to one or more of the following fields to work in our research facility near Boston MA: EARTHQUAKE: The position requires individuals with a Ph.D. degree in geology, engineering or related discipline to plan and conduct both basic and applied research related to Earthquake Engineering including seismology, ground motions and hazard maps structural analysis, structural dynamics and vibrations and shake table tests. Mostly Computational work, experimental for shake table tests. EXPLOSIONS/TERRORISM: The position requires individuals with a Ph.D. degree to plan and conduct both basic and applied research related to Explosions/Terrorism including structural dynamics/mechanics, strong shock analysis methods ranging from simplified methods based on semi-empirical PI relationships to high-fidelity dynamic numerical analyses. Mostly Computational work. WIND: The position requires individuals with a Ph.D. degree in structural engineering, civil engineering or related discipline to plan and conduct both basic and applied research related to Wind/Structural Engineering including wind loading, structural response, full-scale and wind tunnel tests and CFD analysis. Mostly Computational work, may involve experimental work. FLOOD: The position requires individuals with a Ph.D. degree to plan and conduct both basic and applied research related to Flood including hydrological and hydraulic modeling, development of GIS applications and Digital Terrain Modeling. Mostly computational work. Please email resume as an attachment to: jobs@cwsciences.com Commonwealth Sciences, Inc. <a href="http://www.cwsciences.com" rel="nofollow">http://www.cwsciences.com</a>]]>

<![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a QA Analyst to work for a leading San Diego biotechnology company. QA Analyst This Quality Assurance Analyst is responsible for overall development, implementation, maintenance and performance of the Quality Assurance System. In addition, they will interface with other departments to ensure compliance with all applicable regulatory requirements by performing the following duties. -The key responsibilities include develop, implement and maintain Quality Assurance programs that include: *Document control procedures. *Standard Operating Procedures. *Manufacturing Control Systems. *Good Manufacturing Practices. *Product Specifications and Certificates of Analysis. *Product Quality Reviews. -Develop and maintain documents/records pertinent to Quality Assurance activities, such as specifications, labels, MSDS, certificates of analysis, and investigation reports. -Identify and resolve issues to ensure that QA and Operations work effectively and adhere to appropriate standards for all quality programs. -Conduct audits of suppliers, contract analytical laboratories and toll manufacturers to ensure compliance with cGMP and quality requirements. -Review SOPs and batch records, review documents and write reports for test articles used in safety and toxicology testing and clinical trials. -Establish effective partnerships with internal staff to facilitate the timely identification and resolution of compliance/quality matters and other opportunities for quality process improvement. -Perform company cGMP and quality system training. Requirements -Bilingual in English and Spanish is a plus -Must have 4-6 years Quality Assurance experience in FDA or ISO regulated industry. -Experience with food regulations is a plus. -Extensive experience and knowledge of cGMPs and quality systems -BS in Biochemistry or similar scientific discipline. Please visit our website to view additional opportunities in San Diego County: www.biophaseinc.com]]>

<![CDATA[Our client is a full-service contract research organization and consulting firm, helping emerging and established firms commercialize novel and innovative medical devices, in vitro diagnostics, and combination products. They are seeking a Clinical Research Associate (based in San Diego) to work with other clinical services staff and clients, and to be responsible for reviewing all aspects of clinical trials. This is an exciting position, and you will enjoy working for an established, exciting, small company. DUTIES AND RESPONSIBILITIES The primary duties and responsibilities are: assisting in the review of all aspects of clinical field trials conducted to determine performance of medical devices in a controlled medical environment including: -Monitoring medical device clinical trials by making frequent phone calls, sending correspondence and conducting site visits to assure accurate and consistent application of protocols, good clinical practices, appropriate data review and quality control. -Conducting on-site audits to provide orientation and training for investigator and staff, to verify source documentation, data collection process and the timeliness of the trial progress. -Conducting ongoing review of patient enrollment status, case report form (CRF) utilization and other required documentation for review and assessment by Clinical Trials Manager. -Collaborating with Clinical Trials staff on improving protocol development, case report form design, and study handbook development. -Possibly conducting pre-investigational visits to investigator sites, as required. -Quality control of data, prior to and after its entry into an electronic database. EXPERIENCE/SKILL REQUIREMENTS: -One to two years of experience as a Clinical Research Associate or Clinical Study Coordinator, preferably in the area of medical devices. -Knowledge of appropriate FDA regulations and guidelines. -Knowledge of Good Clinical Practices. -Excellent verbal and written skills, superior communication skills for site/sponsor contact. -Willingness to travel at least 50% of work time. EDUCATIONAL REQUIREMENTS: Bachelors or advanced degree in health sciences or nursing.]]>

<![CDATA[Scientist Xen Biofluidx Inc. Location: San Diego, California-San Diego Position type: Full time Area(s) of expertise desired: Conjugation Surface Chemistry and Assay Development, Research, Lateral Flow Assays. Requirements: Ph.D. in chemistry with 2-3 years relevant experience in assay development or BS with a minimum of 10 years. Description We are seeking an independent chemist and assay developer to join an exciting small company that will continue to grow and realize enormous market potential. This is a high-energy job with opportunities for innovative development and personal growth. Major responsibilities include: • You will perform bench work approximately 90% of the time; candidate should be able to adapt innovative technologies and analytical tools into leading edge research. • Provide technical leadership in the areas of analytical and conjugation chemistry. • Knowledge in surface chemistry and detection technology as well as lateral flow assays is highly desirable. • Organize data into meaningful reports and presentations. • Develop protocols, assays, and other relevant procedures to enhance assay performance. • This role is expected to manage several projects simultaneously; be highly flexible and deliver results against aggressive timelines. Qualifications: • Strong background in organic and surface chemistry. • Expertise in analytical methodology and assay development is highly preferred. • Demonstrated ability to be well organized, able to work independently, plan and execute experiments and interpret results. • Strong written and verbal communication skills are highly desirable. • Flexibility and a willingness to work with in a challenging and fast-paced research and development setting are essential. ]]>

<![CDATA[Scantibodies Laboratory, Inc, one of the largest Biotech companies in San Diego is crurrently looking for a Senior Chemist in the Pregnancy Test Kit Formulations Department. Description: Preparation of all PTK and OV, and other lateral flow rapid test reagents, including Gold and Biotin probes conjugations and striping solutions. Understand all Standard Operating Procedures related to Pregnancy Tests Kits and other lateral flow rapid test manufacturing and QC testing. Requirements: BS Degree in life science field is required with minimum of three years of industry experience with cGMP and ISO requirements. Good communication skill is needed. Teamwork and versatility is desired. Benefits include: Medical, Dental, 401K, tuition reimbursement and incentive compensation. ]]>

<![CDATA[Our client is looking for an experienced Executive Assistant to join their team on a long term temporary basis. Duties will include word processing, meeting coordination, spreadsheets and graphs, etc. Excellent written and oral communication skills are required. Only apply if you are a positive team player. Bachelors degree or equivilant experience required. Office/secretarial certification preferred. In all that we do at Davidson Legal Staffing, our aim is to demonstrate The Davidson Difference. It means calling you when we say we will, representing only the best companies in California, and providing the best technology and service to make your job search easy and successful. If you want to work with the best job search firm for the legal, IT and professional services industries, then work with Davidson Legal Staffing. For consideration, please email resumes to Craigsd5@davidsonstaffing.com ]]>

<![CDATA[Cyntellect, Inc. develops and commercializes proprietary products for high-throughput imaging and laser-based manipulation of living cells. Cyntellect combines expertise in high-speed imaging & computing, laser-based medicine, and automation to develop products that are used in applications including drug discovery & development, and stem cell & cell therapy research. The company’s growing list of customers includes major pharmaceutical and biotechnology companies and leading academic institutions throughout the world. The Biomedical / Manufacturing Electronics Technician will successfully design, test, troubleshoot and transfer to production electronic designs for instrumentation projects focusing on instrument performance and reliability of integrated systems. ESSENTIAL DUTIES AND RESPONSIBILITIES: Develop data acquisition means and general bench test equipment to monitor and evaluate performance and reliability of component parts and/or of a complex electromechanical process instrument. Design test methods; cooperate with other technical disciplines to build appropriate test setups and/or custom fixturing; record results and author test reports. Troubleshoot test failures and integrated instrument failures to root cause, and work with a team to recommend and implement design improvements, and potential product enhancements. Analyze and write relevant standards and procedures. Maintain project documentation in accordance with internal standards and external regulatory requirements. Conduct test procedures in accordance with established safety procedures and applicable regulatory requirements. Perform other related duties as assigned. EDUCATION AND EXPERIENCE: BS degree or equivalent experience, in electrical engineering or other engineering discipline. 5 - 10 years experience in manufacturing, and/or servicing of complex software driven electromechanical devices. Experience with one or more of the following is preferred: development of bench type test fixturing for electromechanical subassemblies, experience with embedded firmware, data acquisition systems (analog & digital), complex circuit design particularly I/O interfacing to microprocessor based control systems, reliability assessment through empirical means. Demonstrates technical proficiency, creativity and the ability to manage and direct other engineering staff. Must be a proactive problem solver. Ability to function both independently and as part of an interdisciplinary team. Ability to manage small projects from concept to completion. Must be innovative and entrepreneurial, but capable of operating in an FDA regulated environment. ]]>

<![CDATA[Description: Lead production chemist for an In Vitro Diagnostic manufacturing company in the San Diego area. Duties: 1) Coordinate with sales and operations to create and maintain production schedules 2) Coordinate the efforts of all production personnel 3) Assist in the compounding and manufacturing of product Requirements: 1) Bachelors degree in biology, chemistry or similar field (business admin. accounting, or management education a plus) 2) 3-5 years hands on experience compounding IVD Reagents, controls and Calibrators 3) 1-2 years supervisory experience 4) Understanding of ISO, FDA, OSHA, and cGMP standards 5) Strong organizational, planning, leadership, and communication skills 6) Computer skills: MS Office, particularly MS Word, Excel and Outlook]]>

<![CDATA[<table width="750" border="3" align="center" cellpadding="0" cellspacing="0" bordercolor="#0000FF"> <tr> <td><table width="100%" border="0" cellspacing="0" cellpadding="0"> <tr> <td><img src="http://jobs.expresspros.com/shared/images/headers/eep-static.jpg"></td> </tr> <tr> <td><table width="100%" border="0" cellspacing="0" cellpadding="20"> <tr> <td><table width="100%" border="0" cellspacing="0" cellpadding="20"> <tr> <td> BioMedical Experience? Detail Oriented? If so, we want to hear from you! At Express Employment Professionals, every day we put people in the right job or career. We’re always hiring good people for top local employers, for positions at all levels. Express Employment Professionals offer job seekers a variety of placement options. Express Employment Professionals has been retained by a fast growing Biomedical Company in Carlsbad to assist in finding the perfect contract Engineer Technician. Responsibilities: <ul> <li>Perform basic test activities <li&g