For one of our clients, a pharmaceutical company based between Geneva and Lausanne region, we are looking for a Regulatory Affairs Officer (M/F):ResponsibilitiesPreparing, reviewing, and submitting regulatory files (dossiers, technical documentation, variations, renewals, etc.).Ensuring compliance with international and local regulations (e.g., FDA, EMA, MDR/IVDR, REACH—adapted depending on the industry).Acting as the main point of contact for regulatory authorities and notified bodies.Monitoring regulatory changes and assessing their impact on the product portfolio.Supporting cross‑functional teams (R&D, Quality, Marketing, Supply Chain) during product development, launch, and maintenance.Maintaining regulatory databases and documentation up to date.Your ProfileDegree in Life Sciences, Pharmacy, Chemistry, Regulatory Affairs, or a related field.Proven experience in Regulatory Affairs within the (pharmaceutical / medical device / cosmetic / chemical / food) industry.Strong understanding of regulatory frameworks in key markets.Excellent analytical, communication, and documentation skills.Ability to manage multiple projects and deadlines with high attention to detail.Fluency in English (spoken and written); additional languages are an asset.
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