You have several years of experience in a GMP-regulated environment – ideally in Quality Assurance – and are ready for a new challenge in a senior, hands-on role? As part of our motivated and supportive six-person QA team, you will be responsible for maintaining and further developing our pharmaceutical quality system, with a strong focus on compliance with GMP guidelines to ensure the consistent quality of our manufactured products. With your expertise, you can make a real impact in a dynamic work environment and enjoy opportunities for professional growth and development.

Your responsibilities include:

• Management of deviations, change requests as well as corrective actions and preventive actions

• Review of equipment qualifications, batch documentation, and product release preparations for clinical studies

• Project planning as well as coordination and active participation in interdisciplinary project teams

As prerequisites for this exciting role, you should hold a university degree, preferably a PhD, in a scientific field such as biochemistry, chemistry, or pharmacy. We require at least two years of hands-on experience in a GMP environment for QA roles, and a minimum of four years for other departments. You must be well-organized, proactive, and thrive in fast-paced settings. Strong teamwork, communication, and the ability to work independently are key to success. Fluency in English is required, and knowledge of German or French is a plus.

Interested candidates are kindly requested to submit a complete application (cover letter, CV and reference letters in PDF format) to Ms. Noëlle Haas, who can also be contacted for additional information by phone (058 521 35 01) or e-mail (Write an email).