Marketing specialist Jobs in Baar

Are you a regulatory affairs expert ready for your next exciting challenge in the pharmaceutical sector? We are currently seeking a Senior Regulatory Affairs Specialist to join a global pharmaceutical leader's local office in Lucerne, Switzerland. This is a long-term opportunity starting in June 2025, running through June 2026, with excellent prospects for professional development and possibilty for an extension or permanent position.

About the Role

In this role, you will support the lifecycle management of pharmaceutical products, including marketing authorizations, renewals, variations, and local labeling. You’ll work closely with internal teams, health authorities, and external partners to ensure timely and compliant submissions while playing a key role in regulatory strategy, especially for product launches in Switzerland.

Key Responsibilities

• Prepare and submit Marketing Authorization Applications and variations for assigned products
• Manage responses to regulatory authority queries and objections
• Provide strategic regulatory input to cross-functional teams and product launches
• Maintain local labeling and packaging materials and ensure high-quality translations
• Ensure accurate use of internal and external regulatory systems and databases
• Contribute to the development and execution of local regulatory strategies

Your Profile

Why Apply?

This is a unique opportunity to be part of a forward-thinking organization where your regulatory expertise will directly support public health and patient access to essential medicines. You’ll work on a diverse product portfolio in an inclusive, high-performing team environment.

Location : Lucerne, Switzerland

Contract Duration : 12+ months

Start Date : Ideally June 16, 2025

If you're ready to make a difference in a meaningful role within regulatory affairs, we’d love to hear from you. Apply now!

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