Senior QA Specialist, QA Project Management

Senior QA Specialist – QA Project Management (f/m/d)

Location:

Visp, Switzerland – Hybrid Work Model applicable. Relocation assistance available for eligible candidates and their families.

Role Overview:
For our Quality Assurance team in Bioconjugates, Visp, we are looking for a dedicated Senior QA Specialist in a fast‑growing, innovative environment. The role supports clinical phase manufacturing and interacts with internal and external stakeholders to represent Quality.

• An agile career and dynamic working culture
• An inclusive and ethical workplace
• Compensation programs that recognize high performance
• A variety of benefits dependent on role and location

• Ensure production of APIs is in accordance with Good Manufacturing Practice (GMP) as a member of the QA team (Bioconjugates).
• Support contract manufacturing and advise members of development, production, and analytical departments on all aspects of GMP.
• Responsible for checking manufacturing documentation for conformity, processing change controls, and reviewing and approving deviations and OOS results.
• Serve as the quality contact for our clients and present during their GMP audits.

• University degree in Life Sciences (Microbiology, Biotechnology, Chemistry, etc.)
• First experience in the GMP environment required, preferably in biopharmaceutical industry.
• Strong communication skills and experience working with stakeholders from different departments.
• Experience with Track Wise, SAP, LIMS, and DMS is a plus.
• Fluency in English and German (written and verbal) is required.

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams manufacture the medicines of tomorrow. We value collaboration, accountability, excellence, passion, and integrity. We are committed to an inclusive environment for all employees.

Ready to shape the future of life sciences? Apply now.

Reference: R72108