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regulatory affairs in Los Angeles

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  1. Program Coordinator at Loyola Marymount University

    Collaborate with the Divisional Student Affairs Research and Assessment Office. Keep apprised of changing federal regulations and disseminate regulatory...

  2. VP Medical Affairs North America at Fairway Consulting Group

    Additional experience in related areas such as clinical development, regulatory affairs or pharmacovigilance could be a plus....

  3. Regulatory Affairs Specialist at Sterling Hoffman Life Sciences

    Minimum 3+ years of regulatory affairs experience. Monitor and decipher the regulatory environment. Work with and lead multi-departmental teams to implement...

  4. Vice President, Research at Cedars-Sinai Health System

    In this capacity, the Vice President interacts with senior level colleagues in research and medicine to lead, plan and monitor scientific and financial...

  5. Sr. Principal Scientist - Microbiology (Manufacturing Experience Required) at firstPRO Inc.

    Operations, Manufacturing/Materials Management, Supply Chain, Corporate and Plant Quality, Manufacturing, Regulatory Affairs, Marketing, Finance, Executive...

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    1. Global Director, Regulatory Affairs

      Location: Los Angeles, CASUMMARY:Established in 2004, this organization has been building award winning, Class II medical devices specifically categorized as neuro-modulation devices designed to benefit people with Stroke, Multiple Sclerosis, TBI, Cerebral Palsy, and Spinal Cord Injury.RESPONSIBILITIES:The Global Director of Regulatory Affairs will direct all Regulatory Affairs activities and ...

    1. Cosmetic Chemist / Regulatory Specialist (San Fernando Valley, CA) at Cosmetics & Skin Care

      2-5 years experience in cosmetic (or other FDA) related industry, preferably regulatory affairs. Personal Care Manufacturing Company is looking for a highly...

    1. Regulatory Affairs Associate (3704)

      Summary:Under direct supervision and responsible for the systems preparation of components, building, validating, quality review, submission to the regulatory authority(ies) and archiving of regulatory dossier in support of Baxalta's products.Essential Publishing Duties and Responsibilities:• Working knowledge of ICH Submission Readiness Standards • Supports the compilation of regulatory ...

    1. Medical Science Director - Managed Care at Relypsa, Inc.

      Adhere to all regulatory and compliance guidelines and company policies in all aspects of scientific dissemination of information, including responses to...

    1. Regulatory Affairs Director

      Our client, a leading biopharmaceutical company, is currently seeking an accomplished Director, Regulatory Affairs to join the team. Here is an overview of the role: 1) Lead activities and documents related to regulatory submissions 2) Prepare regulatory filings and maintain regulatory requirements 3) Review clinical documents 4) Prepare project/study team for FDA and other regulatory health ...

    1. Executive Director of Clinical Care at Department of Veterans Affairs

      Develops and coordinates a quality improvement program to ensure that both clinical and administrative activities are in compliance with standards issued by...

    1. Regulatory Affairs Specialist

      Our client, a leading medical device company, is currently seeking an accomplished Regulatory Affairs Specialist to join the team. Here is an overview of the role: 1) Collect and coordinate information and prepare regulatory documentation for submission to regulatory agencies or to commercial partners 2) Compile materials for license renewals, updates and registrations 3) Establish and ...

    1. Executive Director of Community Care at U.S. Department of State

      Department Of Veterans Affairs. Veterans Affairs, Veterans Health Administration. The Department of Veterans Affairs offers Permanent Change of Station (PCS)...

    1. VP of Regulatory Affairs

      A leading company in the biotechnology industry is currently seeking a VP Regulatory Affairs to join their team. For the right candidate, this is a fantastic opportunity with great growth prospects. Details: 1) Provide management and leadership to the Regulatory Affairs organization in the development and implementation of regulatory strategies and processes to gain product approvals ...

    1. Executive Director of Clinical Care at U.S. Department of State

      Department Of Veterans Affairs. Veterans Affairs, Veterans Health Administration. The Department of Veterans Affairs offers Permanent Change of Station (PCS)...

    1. Senior Regulatory Affairs Specialist

      We are on the lookout for a driven individual with a passion for the medical device industry. One of our clients is looking to add a strong Senior Regulatory Affairs Specialist to their team: 1) Provide support for the Regulatory Department to ensure efficient and compliant business processes and environment 2) Participate in product development teams to ensure international regulatory ...

    1. Regulatory & Hazard Communication Specialist I at IHS

      Experience in product stewardship or regulatory affairs. Ensure the quality and regulatory compliance of MSDSs prepared by others on the Regulatory Services...

    1. Regulatory Affairs Manager

      Our client, a leading medical device company, is looking for a Regulatory Affairs Manager to join their team. If you’re game for a challenge and have the required experience, this could be a great opportunity for you. 1) Maintain all company facility registrations and device listings with FDA 2) Maintain all Health Canada product registrations 3) Interface with company’s EC Authorized Rep to ...

    1. Regulatory Specialist at Nellson Nutraceutical, LLC

      Serve as regulatory affairs liaison in new product development process by providing regulatory support to innovation projects....

    1. Director of Regulatory Affairs

      A brilliant opportunity exists for an outstanding individual capable of fitting in to this very rewarding Director of Regulatory Affairs role. Our client, a leading biopharmaceutical company, is looking to hire someone who can bring in additional value to the role; so if you’re someone who is dedicated, energetic and can ensure thorough attention to detail at all times, this could be the ...

    1. Sterilization and Microbiology Auditor / Expert at Tuv America

      Perform evaluations of regulatory submissions including:. TÜV SÜD America Inc., a global leader in product safety and EMC testing, regulatory affairs and...

    1. Regulatory Affairs Associate (3704)

      Summary:Under direct supervision and responsible for the systems preparation of components, building, validating, quality review, submission to the regulatory authority(ies) and archiving of regulatory dossier in support of Baxalta's products.Essential Publishing Duties and Responsibilities:• Working knowledge of ICH Submission Readiness Standards • Supports the compilation of regulatory ...

    1. Coding Analyst at Molina Healthcare

      Follows regulatory and/or contractual reporting requirements regarding fraud, waste, and abuse. Render provider coding education as appropriate based on coding...

    1. Regulatory Affairs Manager

      Manager of Regulatory Affairs   Description MAIN JOB RESPONSIBILITIES 1. Prepares and manages all aspects of all ongoing and new regulatory submissions, both U.S. (e.g., PMA, IDE, 510(k), PMA Annual Reports, etc.), and international (e.g., CE Technical Files, Design Dossiers, APAC, etc.). Provide regular status updates and activity reports. 2. Provide medical review and assure compliance ...

    1. CPG - Office Administrator at Columbia Pipeline Group

      Maintains up-to-date manuals and regulatory information; Columbia Pipeline Group is committed to regulatory compliance....

    1. 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 key ...

    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 ManagerJob ID: 1687Industry: Biotech/PharmaceuticalLocation: Thousand Oaks, CADuration: 6 Month ContractPay Rate Range: Depends on Experience (W-2 all ...

    3. Associate Regulatory Affairs

      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: Regulatory Affairs AssociateJob ID: 1762Industry: Biotech/PharmaceuticalLocation: Thousand Oaks, CADuration: 18 Month ContractPay Rate Range: Depends on Experience (W-2 all ...

    4. Global Director, Regulatory Affairs

       The Global Director 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 key position ...

    5. Regulatory Affairs Manager - (97716)

      A highly reputable pharmaceutical corporation is looking for a qualified Regulatory Affairs Manager to work in Thousand Oaks, CA.Job Description:The Regulatory Affairs CMC Product team is responsible for execution and/ or coordination of all global regulatory CMC activities, including providing leadership, guidance, and insight to oversee the successful execution and implementation of ...

    6. CMC Regulatory Affairs Manager - Biotech/Pharma

      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 ManagerJob ID: 1687Industry: Biotech/PharmaceuticalLocation: Thousand Oaks, CADuration: 6 Month ContractPay Rate Range: Depends on Experience (W-2 all ...

    7. Regulatory Affairs Associate

      Under general supervision responsible for the coordination and the preparation of documents/packages for regulatory submissions. Review and evaluate technical and scientific data and reports required for submission in support of companies products.Responsibilities:• Track of status and progress of regulatory documentation • Review, edit and proofread regulatory documentation • Assist in ...

    8. Associate Regulatory Affairs

      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: Associate Regulatory Affairs Job ID: 1735 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Duration: 5 Month Contract Pay Rate Range: Depends on Experience (W-2 ...

    9. Regulatory Affairs (Publishing) Associate (3704)

      Summary: Under direct supervision and responsible for the systems preparation of components, building, validating, quality review, submission to the regulatory authority(ies) and archiving of regulatory dossier in support of client's products. Essential Publishing Duties and Responsibilities: • Working knowledge of ICH Submission Readiness Standards • Supports the compilation of ...

    10. 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 key ...

    11. Regulatory Affairs Manager

      • TOP 3 SKILL SETS: Scientific background, Experience with Regulatory Affairs Chemistry Manufaturing and Controls , Experience in working with document management systems ( EPIC) (IMR) including Microsoft Suite.  • DAY TO DAY RESPONSIBILIES / FIRST 30 DAYS: Execution of regulatory filings (ARMC’s, Annual Notifications, CTA Amendments, and Post Approval Changes).  • RED FLAGS: Only clinical ...

      1. Research Navigator, CRS at University of Southern California

        Certification as a Clinical Research Professional ( ACRP , SoCRA) is strongly preferred and certification by the Regulatory Affairs Professionals Society is...

      2. Environmental Specialist at Metropolitan Water District of Southern California

        Liaises with regulatory agencies and professional organizations; Leads, develops, and implements environmental programs to meet regulatory requirements;...

      3. Chemist-I at Planet Pharma

        BROAD-BASED EXPERIENCE OR COMBINATION OF EXPERIENCE, IN PHARMACEUTICAL MANUFACTURING, QUALITY OPERATIONS, REGULATORY COMPLIANCE AND/OR REGULATORY AFFAIRS...

      4. Archaeologist at ICF International, Inc

        Familiarity with southern California cultural resources and associated regulatory environment. A history working with private, public sector clients, and...

      5. Toxicologist at Fairway Consulting Group

        Provides toxicology support for planned US and international regulatory submissions, including authoring the nonclinical components of regulatory dossiers and...