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  • Regulatory Affairs Jobs at Caplin Point - 06 vacancies

    Responsible for Authoring and review of dossiers for submission to US, Canada, Europe, Australia, South Africa and other regulated markets. The Company focused on the emerging markets of Latin America, Caribbean, Francophone and Southern Africa and is today one of the leading suppliers of Pharmaceuticals in these regions, with over 2800 product licenses across the globe.
  • JAMP group Hiring for Regulatory Affairs - B.Pharm, M.Pharm Apply
    Review quality Dossiers in CTD format for new Generic drug submissions, in-line with the guidance and templates. Compile responses to deficiencies and deficiency management for the given portfolio of products.
  • Work as Regulatory Affairs Senior Manager at Bristol Myers Squibb
    Managing the regulatory aspects of projects and products for pre-approval and post approval submissions for biological, new drugs and global and local clinical trials. In addition, participating in project team meetings, by providing regulatory support to ensure compliance with all local requirements.
  • Bayer Hiring Regulatory Affairs Manager
    Masters degree in Life Sciences or equivalence scientific degree with minimum of 5-7 years pharmaceutical industry experience in regulatory affairs with at least 2 years of proven leadership, technical specialist role experience in health authority interactions
  • Vacancy for M.Pharm, MSc as Regulatory Affairs Executive at JAMP Pharma
    Prepare and review the responses to Health Canada requeue and Deficiency Letters in timely manner to ensure prompt regulatory approvals of dossiers under supervision of Deputy Manager.
  • Work as Regulatory Affairs Senior Manager at Genpact Limited
    Masters in Life Sciences. Participate, as needed, on global teams to complete assignments and tasks within a specific task force/project associated with labelling
  • Require M.Pharm, MSc Candidates in Regulatory Affairs at JAMP group
    M.Pharm / M.Sc; Candidates with exposure in the pharmaceutical industry with biologics, preferably in regulatory affairs for highly regulated markets.
  • AstraZeneca Hiring Regulatory Affairs Manager
    Regulatory Affairs Manager in the Regulatory Business Development Post Deal Management group is a regulatory specialist with project management capabilities responsible for both regulatory life cycle maintenance submissions and managing successful application transitions for products that are either divested or acquired.
  • Job for M.Pharm, MSc in Regulatory Affairs Department at Torrent Pharma
    Dossier submission and review of Module 1, 2 and 3. ANDA submission. DCP, MRP, National Filing for various EU countries. 
  • Work as Regulatory Affairs PLCM Executive at Apotex Inc
    A Post-graduate, Graduate degree in Chemistry, Pharmacy, Life Sciences. Candidate should have knowledge about Post-approval change submission requirement and compilation of variation packages for US, CAN, EU, AUS-NZ, ROW markets.
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