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Regulatory Affairs Consultant - Switzerland & Germany
PharmiwebLucerne, CHIl y a 15 jours
Description de posteUniversity degree in a scientific area Several years of experience in regulatory affairs, specifically in German and Swiss markets Experience working with Swissmedic and BfArM 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)
Are you a fluent German speaker with expertise in regulatory affairs? Do you have a passion for navigating the complex world of pharmaceutical regulations in Germany, Switzerland, and the EU? We are seeking a talented and experienced Regulatory Affairs Consultant to join our dynamic team!
The role can be home or office based in various European locations.
Key Responsibilities :
- Provide strategic guidance on regulatory requirements and submissions in Germany and Switzerland
- 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
Ideal Candidate Profile :
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