Regulatory Affairs Manager – Switzerland

A leading life sciences consultancy is looking for a Regulatory Affairs Manager to oversee regulatory submissions, manage a team, and ensure compliance with EMEA and FDA regulations. Candidates should possess a minimum of 8 years in regulatory affairs, with at least 4 years in a managerial capacity. Excellent written and verbal English skills are essential...

We are supporting a pharmaceutical organisation in Switzerland in the appointment of an experienced Regulatory Affairs Manager to oversee regulatory submissions, marketing authorisations and lifecycle management for medicinal products within the Swiss market.This is a hands-on position suited to a highly autonomous, pragmatic and commercially aware...

pAmgen Schweiz is seeking a Senior Associate Regulatory Affairs for Clinical Trials to lead regulatory submissions in Switzerland to Swissmedic and to compile submission dossiers across trials and programs. /ppThe role requires a Master’s or Bachelor’s in natural sciences, strong experience with Swiss regulatory filings, fluent English and German, and...

Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of...

pOur client is a well-established, global pharmaceutical company with over a century of history, specializing in high-quality therapies across key areas such as anesthesia, analgesia, and acute care. Headquartered in Southern Switzerland, the company focuses on continuous innovation to improve drug formulation, safety, and patient outcomes worldwide. /ppTo...

Merck Healthcare in Zug is seeking a Regulatory Affairs Manager on a fixed-term basis to support the maternity leave covering 1 January 2027 to 31 March 2028. You will lead regulatory submissions strategy for new medicinal products and lifecycle management while ensuring compliance with local laws and guidelines.The role requires collaboration with Head...

Merck Group in Zug, Switzerland, is seeking a Regulatory Affairs Manager on a fixed-term contract (1.1.2027– ) to cover maternity leave. You will drive submission strategies for marketing authorizations and life-cycle management for medicinal products, ensuring timely, compliant regulatory work.You will collaborate with the Head Regulatory Affairs and...

pTOFWERK, eine Bruker-Tochter, sucht eine/n Quality Manager (m/w/d) zur Entwicklung, Implementierung und Aufrechterhaltung von Qualitäts- und Regulierungssystemen. Der Fokus liegt auf ISO 9001/13485 und enger Zusammenarbeit mit Zertifizierungsstellen sowie Auditors. Die Rolle umfasst auch 5–10% EHS-Unterstützung. /ppDer Arbeitsplatz befindet sich in...

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Masimo, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint...