Regulatory Affairs Consultant - Switzerland & Germany

Switzerland Job Openings

Parexel

Bern

November 26, 2024

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 Bf Ar M
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

We regret to inform you that this job opportunity is no longer available as it has expired

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