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    Quality & Regulatory Associate - England, United Kingdom - EPM Scientific

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    Description
    The Regulatory Affairs Associate will be responsible for:


    • Keeping up to date with regulatory and legal changes in EU
    • Preparing pre- and post-authorisation regulatory documentation and applications
    • Manage the labelling of investigational medicinal product in compliance with regulatory labelling requirements,
    • Assist in the development of the ongoing global regulatory strategy
    • Applications and submissions to national regulatory authorities as required
    • Post-graduate qualifications in Pharmacy, Biological Sciences, or related disciplines.
    • Pharmaceutical industry experience


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