Regulatory Affairs Team Lead - 12 months mission

• Support the Regulatory Affairs team in the preparation, submission, and tracking of regulatory documents.
• Coordinate with internal departments (Quality, Clinical, R&D, Marketing) to gather necessary documentation.
• Maintain regulatory databases and ensure timely updates of product information.
• Assist in compiling dossiers for product registrations, renewals, and variations in compliance with Swissmedic and EU regulations.
• Monitor regulatory timelines and ensure adherence to submission deadlines.
• Liaise with health authorities and third-party partners as needed.
• Ensure compliance with internal SOPs and applicable regulatory requirements.

• Bachelor's degree in Life Sciences, Pharmacy, or a related field.
• Minimum 2 years of experience in Regulatory Affairs within the healthcare, pharmaceutical, or medical device industry.
• Familiarity with Swiss and EU regulatory frameworks.
• Strong organizational and communication skills.
• Proficiency in Microsoft Office and regulatory tracking tools.
• Fluent in English; French is a strong asset.

• A collaborative and supportive team environment.
• Exposure to international regulatory processes.
• Opportunity to work with a reputable healthcare company in Geneva.
• Competitive compensation through Michael Page.

Michael Page