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regulatory affairs in Denver

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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. Client Care Aide I / CNA I - Wheat Ridge Regional Center at State of Colorado

    Must possess and maintain a current CNA certification in good standing from the Colorado Department of Regulatory Affairs.*. Overall Function of the Work Unit:....

  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. Clinical Research Associate - West Coast Region - Home-Based

      PSI CRO AG - Home-based - West Coast Region PSI is expanding rapidly in the US and seeking highly motivated CRAs. At PSI, we believe employees are our greatest assets. Responsibilities: Project activities and monitoring functions associated for Phase I-IV clinical research studies. Comprehensive understanding of the drug development process, Good Clinical Practices (GCP), and relevant ...

    2. Senior Regulatory Affairs Specialist

      Role and Responsibilities: Position is responsible for securing U.S. and international regulatory clearance or approval for Spine products/accessories, including developing regulatory submissions and documentation. Incumbent is the regulatory interface during the product commercialization process and throughout the entire product life cycle including post-market surveillance.   Participate ...

    3. Regulatory Affairs Specialist

      Kelly Services® has been providing outstanding employment opportunities to the most talented individuals in the marketplace. We are proud to offer a long-term temporary opportunity to work as a Regulatory Affairs Specialist at a prestigious Fortune 500® company working in Broomfield, CO. Important information: This position is recruited for by a remote Kelly office, not your local Kelly ...

    4. In-House Landman III

      GOAL: Work on land and other industry related projects independently or under management direction for domestic and international oil and gas companies. Lead or collaborate on projects with internal and external teams and clients. Advise management on various Land, Legal, and Regulatory matters. Develop strategic solutions and recommend improvements to programs, processes and relationships. ...

    5. Quality_ Scientist I, AS&T

      Job Description: PURPOSE The Analytical Scientist I is responsible for the management of assigned projects. This includes the evaluation, development and validation of methods required for raw materials and finished products. Performs qualitative and quantitative analyses of organic and inorganic compounds to determine the identity, purity and homogeneity of drug substances and products ...

    6. Regulatory Affairs Specialist

        Regulatory Affairs Specialist(JOB OPPORTUNITY)-Boulder, CO  3-4 months++ PAY: OPEN DOE   Sr. Level role, more than 5 years exp required. Person needs to have Med Device experience, worked in a regulated environment and international 510K exp.   • Review all international licenses to confirm appropriate filings • Review historical product and manufacturing changes to confirm ...

    7. Director/Sr. Director

      Job Location - Novato, CA All Relocation Fees will be covered by the company.   Company is a clinical stage biotechnology company committed to bringing to market novel products for the treatment of rate and ultra-rare diseases with an initial focus on serious debilitating metabolic genetic diseases. We are launching five Phase 2 clinical trials and with another preclinical trial in the ...

      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. Regulatory Specialist Job at CENTURA SUPPORT

        The Specialist, Regulatory Affairs will assist with regulatory compliance including state, federal and NCQA requirements, among other regulatory or accrediting...

      5. Clin Research Coord-Lung/Thyroid at University of Colorado

        E.g. Principal Investigator, Study Sponsor, FDA , Data and Safety Monitoring Committee ( DSMC ), Regulatory Affairs Coordinator....