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  1. Global Labeling Manager

    Title: Global Labeling Manager Job ID: 24095 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Duration: 3+ Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate)   Job Details: Support the management of Labeling Information and Regulatory Intelligence by facilitating strategic/ tactical initiatives, projects and by developing/maintaining labeling processes, documentation, tools, metrics, labeling status tracking and reporting.   Responsibilities: Support ...

  2. QA Lab Asociate (Analytical Testing, Sample/Data Management)

    Title: Associate Quality Analytical Laboratories (QAL)-Cell Biology II Job ID: 23887 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Duration: 8 Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate)   Job Details: This position is within the Quality Control (QC) Lab, Bioassay and will be responsible for one or more of the following activities including analytical testing, sample/data management, laboratory support activities, and document management. A ...

  3. Quality Assurance Specialist I

    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 Assurance Specialist I Job ID: 24075 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Duration: 5 Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate)   Job Details: Provide Quality Assurance oversight for global distribution ...

  4. Regulatory Affairs Consultant - Perm - 2757

      Novella Clinical Resourcing has a home-based Regulatory Affairs opportunity available.   Overview: The Director of Regulatory Affairs will play a key role in the development of Medical Device submissions and the implementation of Regulatory Compliance.   S/he will develop strategies for government approval, both US and OUS of clinical and pre clinical trials, provide advice on regulatory requirements, prepare submissions, negotiate their approval, and assure that activities are carried out ...

  5. QC Technician

    Quality Control Technician The Quality Control (QC) Technician is responsible for testing and conducting routine and non-routine analysis for in-process, and finished products in order to maintain product quality across the Markwins Brands of Products. Job Duties : • Collect, measure, and weigh samples of materials. • Conduct routine analysis of pre-production and finished products for texture, color, payoff etc. • Maintain product retains. • Record and maintain quality control documents. • ...

  6. Clinical Research Coordinator

    MSN's client is seeking a Clinical Research Coordinator in Las vegas, NV. The CRC is responsible for supporting clinical research staff and managing new and ongoing clinical research activities. The position includes assisting clinical investigators and research staff to drive projects forward by interacting closely with external clinical research organizations and sponsors. The CRC will adhere to GCP, ICH, and FDA guidelines in the conduct of all study related activities. Duties and ...

  7. Chemist (QAL) II – Analytical Testing, GMP

    Title: Associate Quality Analytical Laboratories (QAL) Job ID: 23950 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Unit: Clinical QC Immunoassay & Bioassay Duration: 12 Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate)   Job Details: This position is within the Quality Control (QC) Immunoassay and Cell Biology Lab, and will be responsible for one or more of the following activities including analytical testing, sample/data management, laboratory ...

  8. Chemist (QAL) II – Analytical Testing, GMP

    Title: Associate Quality Analytical Laboratories (QAL) Job ID: 23950 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Unit: Clinical QC Immunoassay & Bioassay Duration: 12 Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate)   Job Details: This position is within the Quality Control (QC) Immunoassay and Cell Biology Lab, and will be responsible for one or more of the following activities including analytical testing, sample/data management, laboratory ...

  9. Regulatory Affairs Director

    Overview The Director of Regulatory Affairs will play a key role in developing and implementing global Regulatory strategies to secure market access for Class II/III medical devices in coordination with key internal and external stakeholders.  This individual will be the Regulatory subject matter expert for all applicable medical devices. S/he will need to identify, assess and communicate regulatory development and submission strategies, regulatory risks, interface with relevant regulatory ...