Are you a specialist in the quality sector? Have GMP experience? We are looking for you!
About the Client
Our client is a giant in the biopharmaceutical sector. Their state-of-the-art site in the Valais canton is a great place to grow in your career alongside a fleet of international professionals. They are currently looking for a QA specialist that can support the continuous improvement of the QMS system within the manufacturing and development of pharmaceutical compounds and products.
About the Role
This role requires you to be available on-site. You will be supporting the quality department by ensuring the compliance, implementation, continuous improvement, and smooth running of the quality management system across departments.
Responsibilities
- Create and maintain clear, reliable reports on compliance activities and quality metrics like deviations, CAPAs, and change controls.
- Help roll out corporate documentation and standards at the site level.
- Work closely with other teams to align and improve quality processes across the site.
- Drive or support projects that strengthen the Quality Management System (QMS).
- Take part in audits and inspections, and ensure timely follow-up actions.
Requirements
- Degree in Biotechnology, Biochemical Engineering, Biochemistry, or a related life science field (BSc, MSc, or PhD).
- Fluency in English, some proficiency in German.
- 3-5 years of hands-on experience in a regulated industry.
- Solid understanding of Quality Systems, including handling deviations, CAPAs, and change controls.
- Background in GMP environments, ideally within a quality function.
- Project coordination or leadership experience is a plus.
- Familiarity with audit processes is an advantage.
