eBay Classifieds » All ads » Jobs » Biotech, R&D, & science » 

document control in San Francisco Bay Area

(1-23 of 23 ads)
View as:
Categories
  1. Scientist II-3986763

    Job Duties Responsibilities: includes but not limited to the following: Plan, execute and document research experiments, analyze and present data Perform nucleic acid extraction, and quantification from Whole blood, Plasma, buccal cells or other clinical samples. ...

  2. Eli Lilly - Pharmaceutical Sales

      Eli Lilly is the 10th largest pharmaceutical company in the world, and has been creating medicines that help improve peoples' quality of life for more than 135 years. Across the globe, we are a leader in investing in research and development and we also invest in our ...

  3. Eli Lilly - Pharmaceutical Sales

    Eli Lilly is the 10th largest pharmaceutical company in the world, and has been creating medicines that help improve peoples' quality of life for more than 135 years. Across the globe, we are a leader in investing in research and development and we also invest in our ...

  4. REG AFFAIRS PROJ MGR - (14000005T6) (RK) A

    REG AFFAIRS PROJ MGR - (14000005T6) (RK) A Pharmaceutical / Biotech Legal - Regulatory / Compliance Law Full-time United States - California - Santa Clara Jobs ID - 1040501 The Compensation Benefits - Full Bonus Eligible - Yes Interview Travel Reimbursed - Yes Detailed ...

  5. Systems Lab Specialist

      $20.00 Hourly 1 Year Assignment High School GED and some work experience. AS degree preferred but not required. Responsibilities: Responsible for organizing laboratory supplies within the labs, sample prep, refrigerators and cold room. Create buffers and solutions. ...

  6. Mgr. Statistical Programming / FTE / San Francisco Bay Area

    Description Create standard SAS programs and macros to generate report-quality summary tables, listings and graphical presentations of clinical data. Manage a small team of statistical programming contractors Maintain documentation of standard programs and reports used ...

  7. Manager/Sr. Manager, Regulatory Affairs

    Purpose To manage the clinical-nonclinical CMC and CMC aspects of domestic and global regulatory affairs activities in support of gene therapy product development.   General Duties Develop and prepare global regulatory submissions in support of gene therapy products. ...

  8. Scientist -Biology

     Execution of development and design verification studies, assist in development and initiation of technical transfer of kit and QC controls.   Molecular Biology skills and techniques, including but not limit to: DNA/RNA extraction, PCR, realtime PCR, reverse-transcription ...

  9. Technical Writing

      My name is Jessica, and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a/an Technical Writing   position for a prominent client of ours.  This position is located in Berkeley, CA. Details for the positions are as follows:   ...

  10. Sr. Medical Writer

     inVentiv Health Clinical is currently looking for a Sr. Medical Writer to work a permanent position with one of our clients in the Bay Area.  We are looking for: •Draft clinical sections regulatory documents including IND applications, Regulatory Briefing Book Documents ...

  11. Mgr. Statistical Programming / FTE / San Francisco Bay Area

    Description Create standard SAS programs and macros to generate report-quality summary tables, listings and graphical presentations of clinical data. Manage a small team of statistical programming contractors Maintain documentation of standard programs and reports used ...

  12. Associate Director/Director Quality Control and Analytical Sciences

    The Position This position will be responsible for oversight of Quality Control activities performed by contract testing laboratories and contract manufacturing companies, including method development, validation, method transfer, GLP and GMP analytical testing and ...

  13. Purification Associate II

    Pharma client seeks several Purification Associates for a long term contract.Responsible for analyzing in-process samples generated from protein purification processes. Complete all required documentation for proper traceability of a production lot.Operate a variety of basic ...

  14. Scientist II- Cell Biology

    Molecular Biology skills and techniques, including but not limit to: DNA/RNA extraction, PCR, realtime PCR, reverse-transcription PCR, and solid understanding of PCR and qPCR theory and data analysis; Tissue and Sample manipulation and handling; Write clear assay development ...

  15. 4003694 - Purification Associate II

      Responsibilities:   Manufacture recombinant antigens to ensure commercial product demands are met: Responsible for the ordering of required raw materials, reagents, and starting material in preparation for assigned production runs.   Responsible for the thorough ...

  16. Technical Associate - R&D

    BioGenex is seeking a Technical Associate to work as part of the Research & Development team to ensure that revenue and customer satisfaction goals are met.      KEY RESPONSIBILITIES Work with R&D to develop product line extensions and product improvements. Perform ...

  17. Senior Software Engineer

    We are a small, private, medical device start-up company launching our first product. We are looking for a hands-on Senior Software Engineer to support the organization in support of the Company’s goals and objectives. The ideal candidate would have had previous medical ...

  18. Senior Associate, Outsourced Manufacturing-Pharma

    Gilead Sciences, Inc. is a research-based biopharmaceutical company founded in 1987. Together we deliver life-saving therapies to patients in need. With the commitment and drive you bring to the workplace every day, you will be part of a team that is changing the world and ...

  19. Scientist Research and Development

    Job Id # 54185 Scientist  Research & Development Location: Pleasanton, CA Length: 6 Months Description: Responsibilities: includes but not limited to the following: • Plan, execute and document research experiments, analyze and present data • Perform nucleic acid ...

  20. Senior Electrical Engineer

    We are looking for a hands-on Senior Electrical Engineer to support the organization in support of the Company’s goals and objectives. The ideal candidate would have had previous medical device experience. This position will report directly to the Senior Director of R&D. ...

  21. Senior Quality Engineer

      We are looking for a hands-on Senior Quality Engineer to support the Quality Organization in implementing, facilitating, and maintaining the Corporate Quality System for all clinical/commercial products and devices in support of the Company’s goals and objectives. The ...

  22. Scientist II-3986763

    Job Duties Responsibilities: includes but not limited to the following: Plan, execute and document research experiments, analyze and present data Perform nucleic acid extraction, and quantification from Whole blood, Plasma, buccal cells or other clinical samples. ...

  23. Validation Engineer - West Region

    ProPharma Group is an industry leader providing validation, compliance and technical services to the pharmaceutical, biotechnology, medical device and related industries. We offer the excitement of a consistently evolving career. Our team is continually learning and working ...