Posted 2 weeks ago

Key Responsibilities:
· Provide strategic guidance on regulatory requirements and submissions in Switzerland, and the EU
· Support national dossier filings and contribute to centralized dossier preparation
· Offer expert advice on new product applications and lifecycle maintenance
· Lead small-scale projects or work streams, ensuring client satisfaction and project success
· Collaborate with cross-functional teams to deliver high-quality regulatory solutions

Your Profile:
· University degree in a scientific area
· Several years of experience in regulatory affairs, specifically in Swiss and EU markets
· Experience working with Swissmedic and BfArM, and other EU national Health Authorities
· In-depth knowledge of international regulatory requirements
· Strong understanding of EU regulatory landscape
· Excellent project management and client communication skills
· Ability to work independently and as part of a team
· Proactive problem-solver with keen attention to detail
· Fluent English and German speaker (required)

Job Features

Job CategoryREGULATORY AFFAIRS

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