Location: the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.
We are currently looking for a QA Manager (f/m/d) who will serve as a key quality expert in contamination prevention and control within microbial manufacturing operations.
In this role, you will drive GMP quality initiatives and compliance, provide high-level QA expertise, and support inspection readiness for regulatory and customer audits. You will work closely with stakeholders across Quality, Operations and global teams to strengthen risk management and foster a strong quality culture through continuous improvement initiatives.
This role is essential in safeguarding product quality, patient safety, and operational excellence.
What you will get:
An agile career and dynamic working culture
An inclusive and ethical workplace
Compensation programs that recognize high performance
A variety of benefits dependant on role and location
The full list of our global benefits can be also found on https://www.lonza.com/careers/benefits.
What you will do:
Lead the asset specific contamination prevention control strategy, ensuring end to end compliance across microbial manufacturing.
Author and approve critical GMP documentation and records, including: SOPs, deviations, change controls, and risk assessments.
Serve as the primary QA SME during regulatory inspections, customer and internal audits for microbial topics.
Partner closely with cross‑functional teams to identify risks, drive deviation management & continuous improvement, and strengthen contamination prevention control practices.
Guide and influence stakeholders by providing microbiology and QA expertise, ensuring robust quality culture and operational compliance.
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