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Specialist Regulatory Affairs (f/m/d)

The Swiss based Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of pepTides and oligonucleoTides. As a full service provider Bachem offers products for clinical development and commercial applications as well as a comprehensive catalog and exclusive custom synthesis. With 50 years of experience and subsidiaries in Switzerland, the United States, the United Kingdom and Japan, Bachem is the partner of choice for the biotech and pharma industry worldwide.  
Bachem. Leading Partner in Tides 

In order to continue our organic growth, we are constantly looking for talent.

Your tasks

Within our innovative RA team, you will be responsible for:
•    Preparation and submission of regulatory documentation including correspondence with health authorities and customers
•    Development of regulatory pre- and post-approval strategies
•    Regulatory assessment of changes to GMP documents
•    RA representation in project teams

 

Your profile
•    Master or PhD in chemistry or pharmacy or an equivalent qualification
•    Fluent in German and English
•    Flair for presenting scientific facts
•    Committed, creative, solution-oriented, well-structured work-attitude honoring timelines
•    Strategic mindset
•    Convincing attitude and persuasive communication
•    Understanding for concepts and principles
•    Ideally, experience in Drug Regulatory Affairs

 

We offer
We offer an interesting position dealing with complex and diversified tasks in a small, motivated team. In this position, you have the opportunity to steer the strategic regulatory decision for marketing approval activities to the respective API.

 

Interested? Please submit your application with full supporting documents (motivation letter, CV, testimonials, diplomas) via recruiting tool to Fabienne Carabelli (HR Business Partner)