Senior QA Specialist, Project Management

About the role

Lonza is seeking a Senior QA Specialist to support its growing BioConjugates business in Visp, Switzerland. The role combines quality assurance responsibilities with project management to ensure GMP‑compliant production of APIs.

Key responsibilities

• Ensure production of APIs follows Good Manufacturing Practice (GMP) standards.
• Support contract manufacturing and advise development, production, and analytical teams on GMP matters.
• Review manufacturing documentation for conformity, manage change control, and investigate deviations and out‑of‑specification results.
• Act as the quality contact for clients during their GMP audits.

Required profile

• Academic degree in Life Sciences (e.g., Microbiology, Biotechnology, Chemistry).
• Significant experience in the biopharmaceutical industry within a GMP environment.
• Strong communication skills, English fluency and German (B2) proficiency.
• Customer‑focused mindset with ability to manage stakeholders independently.

Required skills

• Good Manufacturing Practice (GMP)
• Project management

What we offer

• Agile career and dynamic working culture
• Inclusive and ethical workplace
• Compensation programs that recognize high performance
• Variety of benefits depending on role and location