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 () or e-mail (). jid8ac69d5a jit0624a jiy25a