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  1. Clinical Data Standards Expert at Chiltern International

    Lead the collaboration between relevant functions (Clinical Operations, Clinical Science, Pharmacology, Data Management, Biostatistics, Regulatory Affairs,…) to...

  2. Account Executive at Tuv America

    TÜV SÜD Canada Inc., a global leader in product safety and EMC testing, regulatory affairs and certification, has immediate openings at our facility in Laval,...

  3. STARLIMS SME/Developer and Configuration Specialist at LabAnswer

    The LIMS SME/Developer and Configuration Specialist will provide product knowledge for installing and configuring StarLIMS LIMS/ELN systems for Food and Drug...

  4. Senior Associate, Regulatory Affairs at Par Pharmaceutical an Endo International Company

    Senior Associate, Regulatory Affairs – Review, prepare and submit regulatory documents for original applications, amendments and supplements;...

  5. Compliance Sr Specialist at Cigna

    Acts as a liaison between the organization and regulatory agencies. Ideal candidate will be a self-starter with a willingness to learn new areas of the business...

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    1. Regulatory Affairs Specialist

      Quest is seeking a Regulatory Affairs Specialist who will be responsible for successfully implementing and scaling the company’s global regulatory and compliance program to support bringing our products to the market globally. The role will ensure that Quest is in compliance with all applicable domestic and international laws, regulations and customs for key markets at both the ingredient and ...

    1. Senior HR Business Partner at Mercedes-Benz: Corporate Opportunities

      (MBRDNA), a Daimler company, consists of five business areas including Connected Car, UI & Telematics, Testing and Regulatory Affairs, Powertrain & eDrive,...

    1. Senior Regulatory Affairs Specialist [16-00896]

      We are seeking a Senior Regulatory Affairs Specialist who will develop regulatory submissions and assessments (in compliance with applicable regulations and standards) to ensure timely global commercialization of products. ESSENTIAL DUTIES AND RESPONSIBILITIES With moderate supervision, responsible for the following Regulatory activities: 1. Develop and implement regulatory strategies and ...

    1. Senior HR Business Partner at MB Research & Development NA

      (MBRDNA), a Daimler company, consists of five business areas including Connected Car, UI & Telematics, Testing and Regulatory Affairs, Powertrain & eDrive,...

    1. Senior Regulatory Affairs Specialist - Contract

      This is a full-time, contract position for approximately 6 months.POSITION SUMMARY:  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.  SPECIFIC DUTIES AND RESPONSIBILITIES: ...

    1. Medical Science Liaison - California at Kyowa Kirin Inc

      Adherence to all company regulatory and compliance policies. Commitment to the highest ethical, legal, regulatory and scientific standards....

    1. Sr. Associate Regulatory Affairs (CMC)

      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: Sr. Associate Regulatory AffairsJob ID: 2462Industry: Biotech/PharmaceuticalLocation: Thousand Oaks, CADuration: 9 Month ContractPay Rate Range: Depends on Experience (W2, no ...

    1. Regulatory Affairs Consultant (QE) at Black Diamond Networks

      Join a team of senior regulatory affairs professionals to assist medical device manufacturer in push to deliver multiple regulatory filings....

    1. Manager, Regulatory Affairs

      POSITION SUMMARY:   The position is responsible for diverse regulatory functions, including but not exclusive to the development of Medical Device submissions and the implementation of Regulatory Compliance.ESSENTIAL DUTIES AND RESPONSIBILITIES:   ·         Prepares submissions and applications to US and OUS regulatory agencies to request approval to conduct clinical trials, to request ...

    1. Medical Science Liaison, CNS Northeast (NJ,PA,MD,VA,WV, KY) at Allergan

      Knowledge of applicable pharmaceutical industry legal and regulatory guidelines. Support research initiatives as requested by Allergan R&D, Clinical Operations,...

    1. Director Regulatory Affairs - Medical Device

      Overview: As part of the leadership team the Director of Regulatory Affairs will play a key role in developing and implementing global Regulatory strategies for Class II/III medical devices 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, ...

    1. MEDICAL STAFF COORDINATOR at Los Angeles County Department of Human Resources

      Conducts routine internal audits of the review process to ensure compliance with regulatory agencies; Supports various Committees by working closely with the...

    1. Regulatory Affairs Associate (4243)

      . Regulatory Operations team member in the Authoring Support Group (ASG) responsible for formatting of regulatory submission documents ensuring that documentation meets Shire’s submission-ready standards under direct supervision.Essential Duties and Responsibilities:This section contains a list of five to eight primary responsibilities of this role that account for 5% or more of the work. The ...

    1. Professor of Practice in Bioprocessing, CMC Regulatory Affairs & Quality at Keck Graduate Institute

      Keck Graduate Institute (KGI) seeks a faculty member in the field of CMC Regulatory Affairs (RA) and Product Quality Assurance (PQA) with the focus on biologics...

    1. Regulatory Affairs Specialist

       Summary: Regulatory Operations team member in the Authoring Support Group (ASG) responsible for formatting of regulatory submission documents ensuring that documentation meet our clients submission-ready standards under direct supervision. Responsibilities: ·         Convert MS Word documents in a legacy format to ISIWriter using a custom conversion tool, ensuring that the correct styles and ...

    1. Vice Chancellor, Administrative & Business Services at University of California - Irvine

      Serves as the chief administrative affairs and business services officer for the campus. And to ensure that University operations are in compliance with...

    1. Director Regulatory Affairs

      Overview: As part of the leadership team the Director of Regulatory Affairs will play a key role in developing and implementing global Regulatory strategies for Class II/III medical devices 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, ...

    1. HOTEL OPERATIONS SUPERVISOR at Ameristar Casino Hotel

      Maintains an appropriate level of community affairs involvement. Adheres to, interpret, support, and explain established company policies and procedures as well...

    1. Regulatory Affairs Specialist

      Primary Responsibility / SummaryA regulatory affairs specialist assists in the implementation of international and domestic regulatory strategies. Help with the preparation, coordination, and compiling of applications to foreign and domestic regulatory agencies. Effectively lead and provide regulatory guidance, in addition to deliver the global regulatory strategy for product development and ...

    1. Coordinator III-Regulatory at L'Oreal USA

      The Regulatory Affairs Coordinator is responsible to support, and maintain procedures in the Regulatory Affairs Department to ensure the compliance of all...

    1. Regulatory Affairs Specialist

      Quest is seeking a Regulatory Affairs Specialist who will be responsible for successfully implementing and scaling the company’s global regulatory and compliance program to support bringing our products to the market globally. The role will ensure that Quest is in compliance with all applicable domestic and international laws, regulations and customs for key markets at both the ingredient and ...

      1. Medical Science Liaison/Sr. MSL Women's Cancer I/O - Northern CA/Reno, NV at AstraZeneca

        Adhere to internal standard processes and comply with regulatory and compliance requirements. The incumbent engages in scientific information exchanges with...

      2. Associate Director, Medical and Scientific Writing, Regulatory Affairs (Palo Alto, CA or Philadelphia, PA) at Jazz Pharmaceuticals

        Experience with a variety of regulatory and clinical documents. Knowledge of ICH and CTD guidelines for clinical and regulatory submission documents....

      3. Clinical Affairs Specialist at Dako

        We are looking for a Clinical Affairs Specialist to join Medical & Clinical Affairs at Dako. As a Clinical Affairs Specialist your main responsibilities will be...

      4. Regulatory Coordinator at UCLA Health

        Work with the Network Regulatory Affairs Team which supports the UCLA/Community Oncology Research and Translational Research In Oncology-US, Inc....

      5. Senior Pharmacovigilance Officer at Chiltern International

        Directors, Medical Affairs; Good understanding of the principles of ICH GCP and regulatory requirements. Proven experience in clinical trials with a strong...