Regulatory Affairs Consultant - Switzerland & Germany

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: University 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) #LI-REMOTE