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regulatory affairs in Milwaukee

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  1. 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...

  2. 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....

  3. 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....

  4. 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...

  5. Regulatory Specialist (Consumer Labeling) at Bostik Inc.

    Bachelor’s Degree in Chemistry, Biology, Toxicology or related field and minimum of 3-5 years working in regulatory affairs function....

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    1. Regulatory Specialist 272.15DM

      :: If you meet the qualifications listed below and would like more information contact Dave at 815-756-1221. Attach resume when responding to this posting :: The Regulatory Specialist will be responsible for providing subject matter expertise to assure regulatory and safety compliance through discipline use and thorough knowledge of regulatory requirements and procedures. Qualifications: -BS ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    2. Medical Writer II

      Our Fortune 500 client is currently seeking a Medical Writer for a 1 year +position. The position is located in Waukesha, WI. In addition to working with the world's most recognized and trusted name in staffing, Kelly employees can expect: - Competitive pay - Paid holidays - Year-end bonus program - Recognition and incentive programs - Access to continuing education via the Kelly Learning ...

    3. Clinical Writer - Medical Writer

      Vivos Professional Services is presently seeking candidates for a Clinical Writer position to be located in an office in the Waukesha, WI area. This role will partner with Subject Matter Experts, Medical Directors and clinical teams to create clinical study related documents in accordance with ICH, regulatory authority, and internal company guidelines. Responsibilities: • Create clinical ...

    4. Clinical Writer/Medical Writer, Pharmaceutical (97859)

       Job Description:  A Clinical Writer is needed for a 12-month contract position at major device company in Mid-West. The Clinical Writer partners with Subject Matter Experts, Medical Directors and clinical team to create clinical study related documents in accordance with ICH, regulatory authority, and/or company’s guidelines. Creates a variety of clinical documents necessary for all phases ...

      1. Regulatory Affairs Specialist at ServSolid

        Regulatory Affairs Specialist. Regulatory Affairs Certification (RAPS). The Regulatory Affairs Specialist works with a team of Regulatory Affairs professionals...

      2. Regulatory Specialists at Management Recruiters of Lake County

        The Regulatory Affairs. The Regulatory Affairs Specialist writes, files, and. And Medical Affairs. Global regulatory expectations and requirements....

      3. Animal Originated Tissue Expert at Tuv America

        Perform evaluations of regulatory submissions including:. Perform regulatory audits of clients per European Medical Device Directives (AIMD, MDD, IVDD),...

      4. Regulatory CMC Technical Lead at Advanced Clinical

        This individual will actively partner with development teams, manufacturing, QC and regulatory affairs therapeutic area counterparts to establish alignment with...

      5. Prin Medical Writer at Medtronic

        Collaborate with regulatory teams on all phases of regulatory submissions and approvals, including clinical document preparation and review, regulatory document...