As part of the Quality Assurance (QA) team you will responsible in a shared position with the strategic manager quality assurance for maintaining and expanding the pharmaceutical quality system. The focus is on compliance with Swiss and European GMP guidelines.

Your responsibilities include :

• Management of GMP documentation and ensuring compliance with national and international standards
• Responsibility for a small team
• Responsibility for the internal audit and inspections by authorities
• Responsibility for preparing batch documentation for certification by the responsible person for clinical trials
• Participating in core quality assurance tasks, for example writing and reviewing deviation, CAPAs, change requests, SOPs, qualifications, and validations
• Active involvement in interdepartmental projects teams (process engineering, production, quality control)

As prerequisites for this exciting and challenging job, we expect a university degree (e.g. biochemistry, chemistry, pharmacy). Existing practical work experience in a GMP environment of at least 5 years is required. You have excellent interpersonal skills and experience in leading a small team. You are an analytical thinker and maintain the overview even in hectic situations. You show initiative and entrepreneurial spirit and are excited to participate in the dynamics of an innovative start-up company. You are fluent in English and knowledge of German or French is beneficial.

Interested candidates are kindly requested to send their application documents to Ms. Jacqueline Camenzind, who can also be contacted for additional information by phone (058 521 35 01) or e-mail ([email protected]).

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