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    1. IVD Quality Engineer at DxTerity Diagnostics

      Assists in the implementation and execution of the DxTerity Regulatory Affairs Strategic Plan. Under the direction of the Vice President and Director, Quality...

    2. Senior Regulatory Affairs Specialist Abbott Medical Devices (PDP Program) at Abbott Laboratories

      Regulatory Affairs related internship/co-op/work experience. Rotate through three one-year challenging, demanding and diverse Regulatory Affairs assignments....

    3. Regulatory Affairs Specialist I at Planet Pharma

      Under the direction of senior regulatory affairs staff, assists with processing and archiving of regulatory submissions for the company and partner sponsored...

    4. Regulatory Leader- AgroFresh at The Dow Chemical Company

      Position within the regulatory affairs team. Join the AgroFresh R&D business and be part of this dynamic regulatory team....

    5. Recruitment Professional at IBM

      IBM Corporate Headquarters could be the place for you if you have interest or skills in Finance, Human Resources, Marketing and Communications, Legal and...

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    1. Regulatory Affairs Associate

      Kelly Clinical Research is seeking a Regulatory Affairs Associate for a contract opportunity in Westlake Village, CA. The Regulatory Affairs Associate will be responsible for formatting regulatory submission documents ensuring that documentation meets the company submission-ready standards under direct supervision.Essential Duties and ResponsibilitiesConvert MS Word documents in a legacy ...

    2. CMC Regulatory Affairs Manager

      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: CMC Regulatory Affairs Manager Job ID: 1687 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Duration: 6 Month Contract Pay Rate Range: Depends on ...

    3. CMC Regulatory Affairs Manager

      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: CMC Regulatory Affairs Manager Job ID: 1687 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Duration: 6 Month Contract Pay Rate Range: Depends on ...

    4. Manager Regulatory Affairs

      Hi Elvia,   ***Hiring managers are moving quickly for this position - Please contact me with anyone you may know that fits this background***   I was reaching out to network in regards to a Sr Staff Regulatory Affairs Specialist position (description below) in Chatsworth, CA. Your background seems to be a great fit for the position and I was hoping to speak with you just for a few moments ...

    5. Regulatory Affairs Mgr-1687

      • WHY IS THE POSITION OPEN: This position has been opened to provide support drug product programs due to the acceleration of the AMG145 programs. Writing files for the program. • TOP 3 SKILL SETS: Scientific background, Experience with Regulatory Affairs Chemistry Manufacturing and Controls , Experience in working with document management systems ( EPIC) (IMR) including Microsoft Suite. • ...

    6. DIRECTOR OF REGULATORY AFFAIRS

        DIRECTOR OF REGULATORY AFFAIRS   OVERVIEW Immediate opening for a Global Director of Regulatory Affairs in Valencia, CA who possesses: BA/BS or MS degree in Life Sciences, Engineering, or health care-related discipline 10+ years of experience in the medical device industry Must have extensive experience developing, writing, and overseeing all aspects of the IDE/PMA/510(k)'s process. ...

    7. Global Director / Manager Regulatory Affairs

       The Global Director / Manager of Regulatory Affairs will direct all Regulatory Affairs activities and will have responsibility for providing significant input regarding worldwide strategy, planning, execution and budget. This individual takes the lead to develop, propose and implement regulatory strategies for new products, changes to existing commercial products and new indications. This ...

    8. Quality Assurance & Regulatory Affairs Associate/Specialist

      Summary: This individual reports to the QARA Manager and performs assigned tasks and responsibilities including medical device and product registrations, preparing Technical Files (DMRs), maintaining QMS documents, assisting internal audit, performing regulatory research and impact analysis, as well as handling Complaint/MDR/Vigilance. This is an entry-level position. Responsibilities ...

    9. Senior Regulatory Affairs Specialist

      Working with minimal supervision, manage complex projects/products, including responsibility for the content, assembly, pre-final review, and filing of major medical device applications (e.g., IDEs, PMAs, 510(k)s) submitted to the FDA and foreign regulatory agencies. Applies regulatory expertise to the evaluation and solution of product development issues.   SPECIFIC DUTIES AND ...

    10. Regulatory Affairs Associate (3573)

      Responsible for converting and formatting of regulatory submission documents ensuring that documentation meets client's submission-ready standards under direct supervision. Essential Duties and Responsibilities: • Convert MS Word documents in a legacy format to ISIWriter using a custom conversion tool, ensuring that the correct styles and formatting are applied to the document • ...

    11. Regulatory Affairs Associate (3573)

      Responsible for converting and formatting of regulatory submission documents ensuring that documentation meets client's submission-ready standards under direct supervision. Essential Duties and Responsibilities: • Convert MS Word documents in a legacy format to ISIWriter using a custom conversion tool, ensuring that the correct styles and formatting are applied to the document • ...