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Regulatory Affairs Strategic Liaison Sr. Specialist

Bachem is a leading, innovation-driven company specializing in the development and manufacture of peptides and oligonucleotides. With over 50 years of experience and expertise Bachem provides products for research, clinical development and commercial application to pharmaceutical and biotechnology companies worldwide and offers a comprehensive range of services. Bachem operates internationally with headquarters in Switzerland and locations in Europe, the US and Asia. The company is listed on the SIX Swiss Exchange. For further information, see

We are looking for an experienced RA professional (permanent position, 100%, f/m/d) with excellent communication skills and a business mindset who provides value-added input to internal stakeholders and clients.
You will take full responsibility for your assigned projects/tasks while benefiting from a strong collaboration within our small and motivated team. 
Your tasks

Within our innovative RA team, you will be responsible for:

  • Effectively promote RA Services in client interactions to support Bachem's NCE business

  • Negotiate and implement regulatory support options with internal and external stakeholders

  • Provide RA Advice to NCE CMC development projects teams

  • Develop, present and defend regulatory strategies 

  • Represent RA in project teams for developmental NCEs

  • Simultaneously handle various projects with different support needs  

  • Coordinate project-related RA-activities and keep the RA team up-to-date on the projects

  • Share learnings and experiences within the team


 Your profile

  • Master or PhD in chemistry or pharmacy or an equivalent qualification

  • Solid understanding of and practical experience in Drug Regulatory Affairs (Quality); dossier writing experience is a plus

  • Excellent communicator, fluent and persuasive in English and - as a plus - German

  • Strategic, creative, solution-oriented, pro-active mindset

  • Business and client affinity

  • Self-motivated, committed, well-structured work-attitude

  • Ideally, experience in CMC development and in project work within the pharmaceutical industry


We offer

We offer an exciting and challenging position in a dynamic environment that guarantees you diversity. You will be joining a team of qualified specialists and you will be able to develop yourself professionally. In addition, we offer you the opportunity to work in an innovative environment and in a motivated team. You can expect modern terms of employment and attractive fringe benefits.



Please submit your application with full supporting documents (motivation letter, CV, testimonials, diplomas) online via Recruiting-Tool.