Senior Regulatory Affairs Specialist

Job Title: Senior Regulatory Affairs Specialist

Location: Lucern

Salary: Up to 63.00 CHF per hour

CK QLS are recruiting for a Senior Regulatory Affairs Specialist, to join a growing biopharmaceutical company, at their site based in Lucern. The position is offered on a 12 month contract, with the possibility of extension.

Senior Regulatory Affairs Specialist Role:

• Ensure timely preparation and submission of new local Marketing Authorization applications for assigned products as well as appropriate follow-up with the local authorities.
• Track process and manage answers to objections from the regulatory authorities on products registration and major new indications, involving negotiations to achieve best conditions.
• Participate in subsidiary product and launch teams to provide regulatory input and strategy advice.

Further Responsibilities will Include:

• Maintenance of assigned, authorized products through timely submission of variations, renewal applications, and supplemental marketing authorizations.
• Timely preparation and maintenance of local labels and packaging materials.
• High quality translations and check of labels.
• Efficient and consistent implementation and use of internal and external regulatory databases and systems in Switzerland.

Your Background:

• Master’s degree in Pharmacy or another relevant life science discipline.
• At least 2 years of experience in a registration department, regulatory agency or another related environment in Switzerland.
• Fluency in German and English is required, good level of French and/or Italian (reading documents).
• Familiarity with Swiss and (if applicable) EU legislation procedures and guidelines governing pharmaceutical products; knowledge of the regulatory framework for vaccines is advantageous.

Apply:

Please could you send any correspondence in English. Please quote job reference 133 938 in all correspondence. It is essential that applicants hold entitlement to work in Switzerland.