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For one of our clients located in Ixelles, we are looking for a "CMC Regulatory Affairs".

Job description

International Regulatory experience for full registration Vaccines dossiers (not local experience). - OPERATIONAL ROLE - Coordination of all steps of registration process (not strategic) - Area concerned is the rest of the world (not US - not Europe - not Japan) - Compilation of files following local regulatories + follow-up + maintenance for Vaccines - Only contact he/she will have is internally (with the affiliates) - RA Support - works independently


  • Execution of European Regulatory CMC strategies, submissions and compliance activities for biopharmaceutical projects/products from development to market and post-marketing, including the preparation and submission of correspondence and applications (IMPD's, MAA's) to regulatory agencies. Potential project responsibilities may include monoclonal antibodies, other recombinant proteins, vaccines, peptides and nucleotides. Depending on experience, may act as CMC liaison with regulatory authorities to discuss and define submission contents and strategies.
  • Preparation of CMC information for submission to EU regulatory agencies, generates CMC strategies, assesses risks and develops contingency plans. Ensures that CMC regulatory submissions are complete, properly formatted, and comply with applicable regulatory requirements. Support preparation of interfaces with Boards of Health, including scientific reviewers, administrative staff in order to discuss and define regulatory applications (Quality Module, Responses, Commitments. Depending on experience, may act as CMC representative in formal meetings and teleconferences with regulatory authorities.
  • Life Cycle Teams and compliance of commercial products.
  • May operate independently to resolve issues and manage regulatory risks and ambiguous situations within project teams

Do the above responsibilities fit you like a glove?
Upload your CV and motivation letter via the "apply now" button and you can expect feedback from us soon.
If something is not entirely clear, you can reach out to us by telephone of course.

Team Leadership, Health care, Communication, Maintenance, Science, Vaccine, Strategies, Biopharmaceuticals, Manufacturing, Content Strategy, MSC, Affiliate marketing, Correspondence, Regulatory Risk, Quality assurance, Coordination, Policy, Interfaces, Supportworks, Market Development, Product Development, Administration, Regulatory Affairs, Engagement, Science, CMC


Oxford Global Resources, Ixelles
Quality / Security / Environment, Maintenance, IT, Sales
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