Head of QA Support

vor 45 Minuten

Visp, Schweiz Lonza Vollzeit

Location: the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. The Senior QA Manager (f/m/d) is a member of the QAOperationsUnit andresponsible for overseeing QA Documentation Team and QA Shop Floor teamensuringthe QA oversightand shop floor presenceover the Drug Product area in all matters of cGMP in compliance with national/international requirements and standards. What you will get: An agile career and a dynamic work culture. An inclusive and ethical workplace. Compensation programs that recognize high performance. In addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. Our full list of tailored local benefits can be found below. Benefits in Visp: What you will do: Plan,leadand coordinate: QA Oversight activities, including implementation of the QA Oversight program and execution of QA Oversight during APS and during routine Manufacturing and testing activities per QA Oversight plan. QA review and approval of Aseptic Processing Simulations (APS) process, including implementation of APS strategy, set-up of APS annual plan, APSprotocolsand APS reports Batch Record Review (paper documentation and Manufacturing Execution Systems (MES)) MES implementation (QA representative in the project) Archiving of documents (e.g.paper copies or scans for true copy) Lead Deviation Review Board (s) meetings Provide GXP-related trainings to Module D Operations personnel Author, review and approve GMP-relevant documents and SOPs.  Support continuous improvement programs toestablishan effective Quality Management System for DPSVisp Prepare batch release documentation package for the responsible person (FvP), including completion of release related items (DRs, CRs, INV, CAPAsetc) and recommendation on disposition status, to ensuretimelyrelease activities. Support QA PL for Customer managementin regards toQA Operations topics (change controls, deviations, technical complaints, out of specification results, quality agreements) What we are looking for: University degree or equivalent in Chemistry / Biology / Biotechnology or a related field ExperiencedinPeople Leading andStrategic role Experience in a QA departmentspecificallyDrug Productis valuable Fluent English language skills arerequired, German language is an advantage About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board. Ready to shape the future of life sciences? Apply now. Reference: R72101

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