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    Sr. Regulatory Affairs Specialist - Molecular Pre-Market
    CyberCoders | Saint Louis, Missouri
    Sr. Regulatory Affairs Specialist - Molecular Pre-Market Regulatory Affairs Specialist - Export Compliance - Skills Required - Regulatory Affairs Specialist, Molecular Pre-Market, In Vitro Diagnostics Devices, Medical Devices, Biologics, FDA submissi
    Apr-03-2014
    Senior Quality & Regulatory Associate (Pharma)
    Gallus BioPharmaceuticals | Saint Louis, Missouri
    s: Job Summary / Objective The candidate filling this position will be an experienced regulatory affairs professional with a demonstrated track record of coordination and preparation of complex regulatory submissions and technical files for biopharma
    Apr-03-2014
    Senior Manager, Regulatory Affairs
    Rayovac Remington | Saint Louis, Missouri
    United Industries Corporation, a Spectrum Brands Company, is a leading manufacturer of value brand consumer products for the lawn and garden care and insect control markets. Well known brand names include Spectracide, Garden Safe, Cutter, Repel, Hot
    Apr-03-2014



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    Regulatory Document Specialist
    Express Scripts | Kansas City, Missouri
    **Brief Description:** Fulfill requirements of processing and reviewing regulatory documents according to project specifications and applicable SOPs with adherence to FDA Regulations, ICH/GCP Guidelines and good documentation practices. In addition,
    Apr-03-2014
    Specialist, International Regulatory Affairs
    Boehringer Ingelheim | Saint Joseph, Missouri
    **_Description:_** To independently initiate information gathering, compilation and publishing activities to ensure that all required submissions are prepared and submitted within established timelines. Proactively interact with senior colleagues to
    Apr-03-2014
    Associate II, Regulatory Affairs
    Boehringer Ingelheim | Saint Joseph, Missouri
    **_Description:_** Maintain working knowledge of relevant regulations, policies, and guidelines. Lead in update and maintenance of relevant regulatory databases (Trackwise, CPD3, BIRDS). Support Post Approval RA as needed in ensuring compliance of r
    Apr-03-2014
    Senior Associate, Regulatory Affairs
    Boehringer Ingelheim | Saint Joseph, Missouri
    ***Description:*** Maintain working knowledge of relevant regulations, policies, and guidelines. Review scientific/technical information to compile and author periodic regulatory submissions to appropriate agencies with the purpose of updating produ
    Apr-03-2014


     
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