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Regulatory Affairs Consultant - Switzerland & Germany

Switzerland, Remote 求人ID R0000027369 Category Regulatory / Consulting
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About this Role

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)

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