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regulatory affairs in New York City

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    1. Regulatory Affairs Associate

      Hello,   My name is Guy and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Regulatory Affairs Associate/Proofreader  for a prominent client of ours.  This position is located in Melville, NY.  Details for the positions are as ...

    2. Contract Manufacturing Associate

      The Contract Manufacturing Associate is responsible for maintaining stability data in the regulated systems, organizing records and creating databases to track manufacturing parameters. This individual is responsible for assisting with vendor relationship management, new ...

    3. Senior Audit Manager – Corporate Functions

      Internal Audit is a global organization of over 1000 professionals covering Citi's global businesses and service to clients and customers in over 180 countries. Citi's Internal Audit division provides independent assessments of the company's governance, risk management and ...

    4. Audit Director - Corporate Functions - NAM

      Internal Audit is a global organization of over 1000 professionals covering Citi's global businesses and service to clients and customers in over 180 countries. Citi's Internal Audit division provides independent assessments of the company's governance, risk management and ...

    5. Senior Manager/Associate Director Regulatory Affairs

      Our client is a stable, yet small biopharma located in NYC and is in need of a Senior Manager Regulatory Affairs. Responsibilities: Responsible for the preparation of regulatory submissions in compliance with global requirements. These may include US IND and related ...

    6. Regulatory Affairs Manager at rapidly expanding biotech

      Position Summary A growing company in New York, NY is in need of an individual who will assure compliance with global pharmaceutical regulations. They need a strong background in the pharmaceutical industry, whether in a manufacturing plant or working with a CMO. This ...

    7. Scientific Administrator

      ~~Position Summary Under guidance, the Scientific Administrator provides high-level professional staff support for scientific aspects of the Department’s basic research, teaching, and research training programs in Genetic Therapies. Position Activities Manages specific ...

    8. Clinical Trials Manager

      Location : Novato, CA   Summary: · Responsible for coordination/execution of all operational aspects of clinical studies, including study start-up, patent enrollment and follow up, study closure activities. Develop and manage study budgets, timelines, and resource ...

    9. Clinical Research Manager Contract

      Relocation Required Relocation Expense will be Provided Location ; Jersey City, NJ   Top Tier Pharmaceutical company (with focus in RESPIRATORY, CNS, Diabetes, Cardio, GI and more) in Jersey City, NJ is looking for three Clinical Trials Manager Consultants for Clinical ...

    10. Clinical Trials Manager

      Location : Novato, CA   Summary: · Responsible for coordination/execution of all operational aspects of clinical studies, including study start-up, patent enrollment and follow up, study closure activities. Develop and manage study budgets, timelines, and resource ...

    11. Clinical Trials Manager

      Location : Novato, CA   Summary: · Responsible for coordination/execution of all operational aspects of clinical studies, including study start-up, patent enrollment and follow up, study closure activities. Develop and manage study budgets, timelines, and resource ...

    12. Regulatory Affairs Medicare Analyst

      PURPOSE:The Regulatory Affairs Analyst performs a variety of tasks that support the Regulatory Affairs Department’s role as liaison to regulatory agencies and assists with coordination of plan-wide regulatory activities. KEY RESPONSIBILITIES: 1.The Regulatory Analyst will ...

    13. Assistant Director  Regulatory Medical Device

      Location : Whippany, NJ Relocation Required Relocation Expense will be provided   • The Assistant Director Regulatory Medical Devices is responsible for providing input into the development, alignment, and implementation of technical regulatory strategies to ensure ...

    14. Clinical Trials Manager

      Location : Novato, CA   Summary: · Responsible for coordination/execution of all operational aspects of clinical studies, including study start-up, patent enrollment and follow up, study closure activities. Develop and manage study budgets, timelines, and resource ...

    15. Clinical Trials Manager

      Relocation Required Relocation Expense will be Provided Location : Novato, CA   Summary: Responsible for overseeing all clinical activities related to one or more clinical trials and performing or managing daily in-house operations associated with the trials. This ...

    16. Assistant Director  Regulatory Medical Device

      Relocation Required Relocation Expense will be Provided Location : Whippany, NJ   Divisions include Specialty Pharmaceuticals, Medical Care, Consumer Care and Animal Health. At this top tier Pharma company you have the opportunity to be part of a culture where they value ...

    17. Quality Engineer

      The Quality Engineer will play a critical role within the manufacturing plant and will function as the subject matter expert on matters related to quality and regulatory affairs. Responsibilities You will prepare, update, maintain and approve all PPAP documentation ...

    18. Clinical Trials Manager

      Location : Novato, CA   Summary: · Responsible for coordination/execution of all operational aspects of clinical studies, including study start-up, patent enrollment and follow up, study closure activities. Develop and manage study budgets, timelines, and resource ...

    19. MD, Clinical Dermatology  -Director or Senior Dir- Relocation Required

      Relocation Required Relocation Expense will be Provided Location : Whippany, NJ   LOOKING FOR DERMATOLOGIST (MD )to work on Very successful 140 million + products Interfacing with Key Thought Leaders and having a gregarious personality are essential! Suppporting Medical ...

    20. Regulatory Affairs Associate - Proofreader

      Hello,   My name is Murv and I represent The Fountain Group.  We are a national staffing firm and are currently seeking an  Regulatory Affairs Associate – Proofreader for a prominent client of ours.  This position is located in Melville, NY. Details for the positions are ...

    21. Contract Manufacturing Associate

      The Contract Manufacturing Associate is responsible for maintaining stability data in the regulated systems, organizing records and creating databases to track manufacturing parameters. This individual is responsible for assisting with vendor relationship management, new ...

    22. SAS Programmer - Relocation Required

      Relocation Required Job Location - Hoboken, NJ   Top tier Pharmaceutical company is looking for SAS Programmer for their growing team. II. PRIMARY JOB RESPONSIBILITIES: Create derived data set specifications for all assigned studies and integrated summaries. Create ...