Head Regulatory Affairs (40-60%) – Join Our Team!

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Are you passionate about regulatory processes and keen to work in a dynamic pharmaceutical environment? We are looking for a Head Regulatory Affairs to join our team at Medvisis. 

You will play a crucial role in ensuring compliance with Swissmedic regulations and managing regulatory activities for our product portfolio. Your responsibilities will include:

• Coordinating and submitting approval dossiers, variations, and renewals
• Managing approvals for launched products, including transfers and deletions
• Tracking regulatory projects and deadlines
• Communicating with Swissmedic and internal stakeholders
• Ensuring compliance with evolving Swissmedic guidelines
• Managing eCTD submissions and regulatory databases
• Supporting audits, inspections, and quality assurance projects

• Completed professional training, ideally in a paramedical field
• Extensive experience in the pharmaceutical industry
• Strong knowledge of Swiss regulatory processes and Swissmedic requirements
• Fluent in German and English (spoken and written)
• Detail-oriented, reliable, and well-organized
• Strong collaboration and communication skills
• Proficiency in digital tools 

• Be part of an innovative and young company 
• Work with a very experienced Leadership Team
• Enjoy a collaborative and supportive work culture
• Leverage agile working methods

If you’re ready to take your career to the next level, apply now and become a key player in shaping the future of regulatory affairs at Medvisis! 

Please send your CV to info@medvisis.com

Our CEO Manuel Ackermann is happy to answer your questions - just give him a call: +41 79 422 14 92