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document control in San Francisco Bay Area

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    1. Drug Safety Associate III (Contract Position)

        Title :  Drug Safety Associate III Location :  Palo Alto, CA Contract (40 hours) – Contract Position  Rate : Negotiable.   The DSA III is someone who is an HCP (RN, PharmD, or MD) who has significant drug safety operations experience who can triage cases for seriousness and reportability. DESCRIPTION As a member of the Drug Safety and Pharmacovigilance department, the Drug Safety ...

    2. Bioprocessing Engineering Associate (10123)

      Title: Bioprocessing Engineering Associate (10123) Location: San Jose CA 95131 United State Time: 8.00 AM to 5.00 PM Work Days: Mon To Fri Duration: 6 Month   Qualifications: MINIMUM QUALIFICATIONS 1.Demonstrated Technical Skills, depending on position needs: Automation, Mechanical Design, Fluid Handling, Protein Chemistry, Immunoassays, Flow Cytometry. 2.Effective written and oral ...

    3. Manufacturing Technician

      The Manufacturing Technician will work in a team environment, following established protocols and processes according to current industry standards. Must have ability to complete activities in accordance with Standard Operating Procedures (SOP), Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP), as well as any applicable federal regulations or Industry standards. ...

    4. Senior Manager, Regulatory Affairs - CMC

      The Manager/Sr. Manager of CMC Regulatory Affairs will be responsible for ensuring the CMC regulatory strategy is in alignment with the global regulatory strategy and lead/coordinate the process for compiling CMC section of regulatory submissions. Key Accountabilities/Core Job Responsibilities: • Reviews CMC documentation to ensures they meet regulatory requirements. • Represents RA CMC at ...

    5. Molecular Pathology Scientist

      Work in a team environment to develop new protocols and redefine processes for efficient manufacturing of molecular pathology products to meet or exceed current industry standards.  Ensure that all processes are completed according to Standard Operation Procedures (SOP), Good Manufacturing Practices (GMP), as well as any other applicable global regulatory standards. Responsibilities Read ...

    6. Environmental, Health & Safety Project Scientist

      ARCADIS is seeking an Environmental, Health & Safety (EHS) project scientist to join our consulting team on challenging projects for a variety of large industrial and global clients and attain career growth. An immediate full-time position is located in the California Bay Area. ARCADIS provides substantial career growth opportunities for professionals in the technical and business consulting ...

    7. Technical Manager

      Technical Manager-Benicia, CA Direct Hire $65-$75K/yearResponsible for providing technical support to the customers. Completing customer quality and regulatory questionnaires. Reviewing quality control data and signing Certificates of Analysis. Conducting mock recalls. Managing the packaging of products including creation and issuance of batch records. Managing the policies, procedures, ...

    8. Regulatory Operations Specialist

        Summary Description: Immune Design is seeking an experienced Regulatory Operations Specialist to support the development, compliance and oversight of electronic submissions/document control programs and policies.   Primary Responsibilities: Responsible for authoring, implementing and maintaining various departmental guidelines, procedures and templates associated with the regulatory ...

    9. SE30 - Quality Control Technician

      Hello, my name is Tony Zarlingo. Kelly Scientific® has been providing outstanding employment opportunities to the most talented individuals in the marketplace. We are proud to offer a long-term temporary opportunity to work as a QC Laboratory Specialist at a prestigious Fortune 500® Pharmaceutical company working in the South Bay of CA. This is a 12 month temporary position at 40 hours per ...

    10. Director SEC Reporting 928

        Director SEC Reporting 928 A new opportunity for a Director of SEC in a growing and exciting biotech company in South San Francisco providing technology to confirm the integrity of applied life sciences.   The Position Manage the preparation of all SEC filings, including quarterly (Form 10-Q) and annual (Form 10-K) periodic filings, related earnings release materials and investor ...

    11. Quality Control Laboratory Specialist

      Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis.   Title: Quality Control Laboratory Specialist Job ID: 2034 Industry: Biotech/Pharmaceutical Location: Mountain View, CA Duration: 12 months Hours per Week: 40   Job ...

    12. Quality Control Laboratory Specialist

       A highly reputable pharmaceutical corporation is currently looking for a qualified Quality Control Laboratory Specialist to work in Mountain View, CA. Description: The Clinical Pharmacology & DMPK Department is seeking a highly motivated individual with strong GLP experience to join the bio analytical group as a QC specialist working on the bio analytical data/report review in support of ...

    13. Bioprocess Technician

       Duties: Responsible for producing innovative biotherapeutic medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment, and maintain areas in high state of inspection preparedness.  Operates production equipment for cell culture or purification that may include culture growth, process monitoring, sampling, harvesting, purification, ...

    14. Quality Control Technician

      Quality Control Associate/Sr. QC AssociateLocation: Mountain View, CA Direct Hire Pay/Salary DOE!We are looking for QC Associates (I, II, III) to perform Flow Cytometry along with basic lab tests (CBC, Hemacytometer, ELISA) for a Cellular Therapy company.MAIN FUNCTIONPerforms daily Quality Control activities under the direction and guidance of the supervisor/ manager in support of Company and ...

    15. Medical Writer

      A Senior Non-Clinical Editor is needed for a 5-month contract position at major biotech company in Northern California.   Responsibilities: Edit, format, proofread, and manage to completion a variety of nonclinical documents for submission to regulatory agencies, including study reports and IND/BLA summaries Coordinate the adjudication of review comments with authors ...

    16. Sr Non Clinical Editor

      Kelly Scientific Resources is the world's most recognized brand in Scientific Staffing with more than 100 locations in the North America, Europe and the Pacific Rim. Our scientists contribute to the research and development of products that are used daily in the home, such as medical devices or pharmaceutical products. We employ more than 700 clinical research professionals and 4,500 ...

    17. Quality Assurance Manager

      Quality Assurance Manager-Petaluma, CA Direct Hire 95K-120K/year Quality Assurance Manger responsibilities include: Maintain a well-defined administrative system for ensuring the following items and activities are properly regulated: standard operating procedure generation and maintenance, distribution tracking of all quality documents, establishment of proficiency testing program, ...

    18. Regulatory Affairs Associate

      Regulatory Affairs Associate Location: Fremont, CA 12 Month Contract Pay Rate: $25.00-40.00/hour DOE Our client is looking for someone to start in early to mid-July for a high profile project. Successful candidates will have a pharmaceutical perspective and understand working in a high demand/pressure environment in order to meet deadlines. This is a great opportunity for a recent Masters or ...

    19. Housing Health and Safety Technical / Analytical Specialist

      Another Source's client, Stanford University, is recruiting a Health and Safety Technical / Analytics Specialist to join their team. Here's a little about Stanford University and the position they are seeking to fill:  The R&DE Student Housing Health and Safety Specialist will join the Manager of Health, Safety, and Environmental Compliance to ensure a safe and healthy place to work for our ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    20. Sr Medical Director - Clinical Development - Oncology & Immunology

      Seeking experienced Medical Director with 4+ years experience in Clinical Development for cancer therapeutics. Key Requirements: *** Medical Doctorate degree and strong knowledge of Oncology, Immunology, Inflammation, or similar. *** Experience in Clinical Development activities for new therapeutics, must have previous role leading Early Stage Clinical Trials. *** Successful ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    21. Cosmetic Study Staff

      Position: Cosmetic Study Staff Company Summary: Company specializing in skin care and beauty product research Position Description: This position is responsible for the implementation phase of consumer testing (safety-in use) for cosmetic products. Job Responsibilities:     Prepare study documents, study folder, review study protocol     Call handling and phone pre-screening possible ...

    22. Clinical Development Medical Director - Neurology

      Lead Clinical Development activities for new drugs treating various Neurological indications. Design and execute clinical trials and run programs for Phases II through IV. Activities: *** Provide medical and scientific expertise to study teams and key stakeholders. *** Lead the development of the clinical strategic plan for therapeutic area. *** Communicate strategic and operational ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    23. Quality Assurance Specialist

      QA Specialist II/ QA Specialist III Department: Quality Assurance Location: Mountain View, CA Direct Hire or Contract-to-Hire Responsibilities • Ensure the timely release of cellular products in accordance with Company and or client procedures and requirements. • Promote compliance with applicable cGMP/GTP regulations and company/client SOP • Provide input based on knowledge and experience on ...

    24. Clinical Pharmacologist

      Kelly Scientific Resources is the world s most recognized brand in Scientific Staffing with more than 100 locations in the North America, Europe and the Pacific Rim. Our scientists contribute to the research and development of products that are used daily in the home, such as medical devices or pharmaceutical products. We employ more than 700 clinical research professionals and 4,500 ...