QA Manager, QA Analytics 80-100% (f/m/d)

Lonza, a global leader in life‑science manufacturing, is looking for a QA Manager to head QA Analytics at its Visp site in Switzerland. The position supports the company's mission to deliver tomorrow's medicines by guaranteeing that quality‑control activities meet GxP, data‑integrity and regulatory expectations while aligning with internal and customer standards. In this role you will act as the QA Analytics voice within cross‑functional groups, presenting quality concerns to QC teams and ensuring that all standard operating procedures are followed. Daily tasks involve reviewing and signing off method‑transfer and validation documents, approving technical records, and overseeing the investigation and documentation of QC deviations. You will make decisions during deviation handling, drive corrective‑and‑preventive actions (CAPA) to closure, and serve as a subject‑matter expert for specific analytical areas, offering guidance to internal and external stakeholders. Supporting regulatory inspections and customer audits also forms part of the remit. The ideal candidate holds an academic qualification in Chemistry, Biochemistry, Biotechnology or a related life‑science discipline and brings extensive experience in pharmaceutical QC/QA environments. Proven expertise in analytical method validation, change and deviation management, as well as a solid grasp of cGMP regulations, including USP, European and Japanese pharmacopeias, is essential. Prior involvement in audits and direct interaction with health‑authority bodies such as the FDA or Swissmedic is required, together with excellent written and spoken English communication skills. A collaborative mindset and the ability to work across functional teams are valued, while German language ability is considered a plus. The Visp location offers a supportive setting with relocation assistance for eligible candidates and their families. Lonza promotes an agile career path, an inclusive culture, and performance‑based compensation, complemented by a range of benefits tailored to the role and site. What the role asks for: - Degree in Chemistry, Biochemistry, Biotechnology or Life Sciences - Deep QC/QA experience in pharma sector - Analytical method validation and change management expertise - Strong cGMP knowledge including USP, EU, Japanese pharmacopeias - Auditing experience with Health Authority interactions - Fluent English communication, both written and oral - German language proficiency beneficial