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Regulatory Affairs Manager (all genders)

Merck Healthcare·Zug·24.09.2026

 careers.merckgroup.com

 
 
full_time80–100%
Required language
German professional, English professional
Job written in
English
Location
Zug
Work type
On-site
Type
Full-time

 

The Regulatory Affairs Manager role is within a global company that innovates in Healthcare, Life Science, and Electronics. The company develops medicines, intelligent devices, and innovative technologies in areas like Oncology, Neurology, and Fertility. The team works across six continents, focusing on improving and prolonging lives. The main responsibilities include developing submission strategies for new medicinal products and managing the life cycle of registered ones. This involves ensuring compliance with external and internal regulations, guidelines, and legal bases. The role also includes reviewing promotional materials for regulatory compliance and maintaining contacts with authorities and subject matter experts. To qualify, candidates must have a university degree in pharmacy, medicine, or natural sciences, and at least five years of experience in regulatory affairs in Switzerland. Fluency in German and very good English skills are required. An analytical and strategic mindset, independence, commitment, and attention to detail are essential. The role demands flexibility, the ability to work under pressure, and a motivation to interact with stakeholders. Nice-to-have skills include a collaborative spirit and the ability to work well in a team. The position is based in Zug and is a fixed-term contract from January 1, 2027, to March 31, 2028, to cover a maternity leave. What the role asks for: - University degree in pharmacy, medicine or natural sciences. - At least 5 years' experience in regulatory affairs in Switzerland. - Fluency in German. - Very good English skills.

 

 

 

 

 

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