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Senior Regulatory Affairs Specialist

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Key Role SummaryWe are seeking a skilled professional to spearhead regulatory affairs for biologicals, vaccines, and small molecules across various markets.Main Responsibilities:The successful candidate will prepare and deliver regulatory submissions from a global and regional perspective.They will develop and review Marketing Authorization Applications & Variations for filing in key regions.Maintaining knowledge of regional trends, global pharmaceutical legislation, and regulatory CMC aspects is crucial.Required Skills:Excellent written and verbal communication skills.Strong organizational and time management skills.Able to work independently with minimal supervision.This is an exciting opportunity for a motivated and experienced regulatory professional to join our team. If you have a strong background in regulatory affairs and a passion for delivering high-quality results, we encourage you to apply.