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Specialist RA I (Development)

Bachem is a listed technology-based company focused on peptide chemistry. The company provides a full range of services to the pharma and biotech industries. It specializes in the development of innovative, efficient manufacturing processes and the reliable production of peptide-based active pharmaceutical ingredients. A comprehensive catalog of biochemicals and exclusive custom syntheses for research labs complete the service portfolio. Headquartered in Switzerland with subsidiaries in Europe, the US and Asia, the group has a global reach with more experience and know-how than any other company in the industry. Towards its customers, Bachem shows total commitment to quality, innovation and partnership.

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

Your responsibilities

We look for an excellent communicator with a business mindset. You will cooperate closely with internal stakeholders and customers, deliver the regulatory position in development project teams, develop regulatory strategies for our APIs, and actively coordinate project-related work within the RA department. You will be solely responsible for various development projects, sharing relevant project information with your team and thoroughly documenting the regulatory history of the projects.


Your qualifications


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

·         At least two years of experience in Drug Regulatory Affairs

·         Fluent and persuasive communication in German and English

·         Strategic thinking and a convincing attitude

·         Understanding for concepts and principles

·         Committed, creative, solution-oriented, well-structured work-attitude

·         Flair for literature and guideline research

·         Ideally, experience in project management within the pharmaceutical industry and in CMC development


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 the respective API.



Interested? If so, Mrs. F. Carabelli will be pleased to hear from you and receive your complete application documents.

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