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regulatory affairs in Jacksonville

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  1. Medical Writer I at Planet Pharma

    Medical writing, regulatory affairs, clinical research, engineering). Ph.D/Pharm D plus 1 to 2 years of related medical device/drug industry experience (e.g....

  2. 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...

  3. Project Leader I, Regulatory Affairs Job at Johnson & Johnson

    He/She assists in the development of best practices for Regulatory Affairs processes and provides Regulatory Affairs support during internal and external audits...

  4. Hiring for Regulatory Affairs Director at

    Director Regulatory Affairs. Hiring for Regulatory Affairs Director. Prefer international regulatory knowledge and submission experience....

  5. Sr. Director, Medical Affairs at Sucampo Pharmaceuticals, Inc.

    The Senior Director of Medical Affairs is a key strategic leader in this structure. This leader will provide insightful medical practice insights to support the...

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    1. Operational Risk Manager

      The BORM Issues Manager is responsible for driving the end to end process spanning the life cycle of a business issueincluding: identification and documentation, root cause analysis, remediation solutioning planning, status monitoring andreporting, and closure activities. These activities will be conducted in close partnership with the Business Issue Owners.• Identifying the Business Owner ...

    2. Regulatory Affairs Specialist (Indirect) (Professional)

      ob Title: Regulatory Affairs Specialist (Indirect) (Professional)  Job Description:  Ensure compliance to the FDA Quality System Regulations, European Requirements, and other regulatory requirements.,Prepare required documentation (510(k)s, technical files, dossiers) for domestic and foreign submissions and registrations. Attend design review meetings regarding design controls. Interacts ...

    3. Regulatory Affairs Specialist

      REGULATORY AFFAIRS SPECIALIST Kelly Clinical Research is seeking Regulatory Specialist candidates in the Jacksonville, FL area for a long term, open ended contract. The Regulatory Specialist is a key documentation expert for the Regulatory Affairs department. This individual is responsible for preparation of internal Regulatory documentation and various document types to be used in dossiers ...

    4. Operational Risk Manager

      The North America Consumer Business Operational Risk Management (BORM) Utility was created with the objective of better addressing the need for an improved and unified approach to operational risk issues and the inefficiencies of the legacy structure. The organizational structure of the utility facilitates common processes, maximizes our talent, strengthens our business process controls, ...

      1. 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....

      2. 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...

      3. Director, Medical Affairs at SynteractHCR, Inc.

        Collaborates with the Global Vice President, Medical and Regulatory Affairs on the ongoing development of the Medical Department and contributes to the business...

      4. Medical Device Auditor at Tuv America

        TÜV SÜD America Inc., a global leader in product safety and EMC testing, regulatory affairs and certification, has an immediate opening at our offices in the...

      5. Quality Management System Auditor at Tuv America

        TÜV SÜD America Inc., a global leader in product safety and EMC testing, regulatory affairs and certification, has an immediate opening for a Quality Management...