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document control in Los Angeles

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  1. 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 ...

  2. 32704 – Scientist II

    Responsibilities: This individual will be responsible for providing assessment of raw material changes, their impact on product, process, supply chain, the qualification requirements for the change requested and execution of the change. This individual will work in a team environment with Raw Material Center, Operations MAKE, Supply Chain, Analytical, Quality Assurance, and Product Deployment technical functions. Qualification of Alternate Raw Materials that are used in products produced at the ...

  3. 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 ...

  4. Validation Engineer II - Job #: 14-01150

     Our client in LOS ANGELES, CA is looking for an Validation Engineer II. This is a long term consulting position.  If interested, Please apply to this ad. Job Title: Validation Engineer II Location: LOS ANGELES, CA Job #: 14-01150 Job description: The current project phase entails assessment of existing WIP Tanks, Product Transfer Lines, Tote Transfer Stations, and High Volume Filling Systems for CIP operation utilizing a new fully automated CIP Stationary System. Cleaning developments will be ...

  5. 32360– Validation Engineer II

    The Cleaning Validation Consultant will be responsible for the executing of cleaning validation protocols on Liquid/Semi solid equipment which include: Tanks or kettles, Mixers, pumps and other equipment associated with liquid and semi solid manufacturing. The consultant may also help to write and review cleaning validation protocols. This individual must be versed in the principles and approaches of product/equipment cleaning validation and will be responsible for providing hands on technical ...

  6. 31550 – Validation Engineer III

    Job Description: The current project phase entails assessment of existing WIP Tanks, Product Transfer Lines, Tote Transfer Stations, and High Volume Filling Systems for CIP operation utilizing a new fully automated CIP Stationary System. Cleaning developments will be completed to assess the most effective cleaning process. Responsibilities: Will be led by a technical lead and will be part of a team performing cleaning cycle developments and cleaning validations. 24-hour shift and weekend work is ...

  7. Quality Operation Technician

    GENERAL DESCRIPTION The Quality Operation Technician is responsible for the execution of multiple projects dealing with quality related functions.   PRIMARY RESPONSIBILTIES 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. This position will be responsible for the following tasks (tasks may include, but are not limited to the following):   ...

  8. Senior Analytical/Validation Chemist

    GENERAL DESCRIPTION   This position is responsible for the coordination, design, execution and oversight of analytical method transfer and validation requirements to support the chemical laboratory.     Must have working knowledge in a pharmaceutical and nutraceutical quality control or development laboratory environment. Ability to perform and operate laboratories test methods and instruments, including HPLC, GC, ICP, FTIR, UV/VIS Spectrometer. Ability to design & validation of new test ...

  9. Data Analyst II

    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: Data Analyst II Job ID: 23941 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Duration: 12 Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate)   Job Details: This position is primarily responsible for ensuring the company’s ...

  10. Quality Operations Inspector

    GENERAL DESCRIPTION   The Quality Operations Inspector is responsible for providing support to the Company’s Quality Operations to ensure that all work performed meets GOP, GMP, and FDA regulatory compliance requirements. Individual is responsible for monitoring quality-oriented operations both internally and externally.   ESSENTIAL JOB DUTIES/RESPONSIBILTIIES To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable accommodation may ...

  11. 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 ...

  12. 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 ...

  13. Cytomentry Expert (BD FACSCantoII, BD LSRII, BD FACSort)

    Title: Cytometry Technician Job ID: 23920 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Duration: 18 Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate)   Job Details: A first or second shift technician position providing on site Cytometry Core support for R&D at a major biotechnology company. The Cytometry Core provides specialist technical support and training in the use of multiple brands and platforms of flow cytometry analyzers and sorters, ...

  14. Biochemist - Flow Cytometry

    Title: Biochemist - Flow Cytometry / Conjugation Technician Job ID: 23924 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Duration: 18 Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate)   Job Details: A first or second shift technician position providing on site conjugation services in the Cytometry Core for R&D at a major biotechnology company. The Cytometry Core provides specialist technical support and training in the use of multiple brands and ...

  15. Project Coordinator I (Document Management)

    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: Project Coordinator I Job ID: 23860 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Hours per Week: 40 Pay Rate Range: Depends on Experience (W2 all-inclusive)   Job Details: Global Research and Development Quality - Standards (GRDQS) leads the development ...

  16. Project Coordinator I (Document Management)

    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: Project Coordinator I Job ID: 23860 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Hours per Week: 40 Pay Rate Range: Depends on Experience (W2 all-inclusive)   Job Details: Global Research and Development Quality - Standards (GRDQS) leads the development ...

  17. 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. • ...

  18. Senior Engineer, Drug Delivery - Electrical Engineering

    Title: Senior Engineer, Drug Delivery - Electrical Engineering Job ID: 23602 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Duration: 12 Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate)   Job Details: Medical Devices include a wide range of devices, such as needle protection systems, fluid transfer devices, pen injectors, automatic pen injectors, and micro-infuser delivery pump systems.    This individual will be acting as a lead for a cross ...

  19. Quality Control Publisher I (Expert in  Adobe Acrobat 7.0)

    Title: Quality Control Publisher I Job ID: 23830 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Duration: 18 Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate)   This position will provide Publishing Quality support for Global Regulatory Affairs and Safety. Perform quality control checks of PDF components for electronic regulatory submissions by adhering to company’s guidelines and use of QC check list. These checks focus on the formatting of and ...