The actual location of this job is in Stein, AG, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. Be part of a dynamic, fast‑paced project environment where no two days are the same—this is a unique opportunity to help build multiple new commercial production lines and shape the future of manufacturing from the ground up. We are looking for a confident and collaborative leader with QA Operations experience in pharma manufacturing, strong stakeholder management skills, and an assertive mindset; experience in aseptic fill & finish is a plus. This role is primarily based on site. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. We offer flexibility to work remotely for no more than 20% of your time. Requests are considered on a case‑by‑case basis, in line with business needs. Benefits
An agile career and 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. Full list of global benefits: https://www.lonza.com/careers/benefits. What you will do:
Lead, develop and grow a team of QA Experts. Create and lead the overall Quality strategy. Partner with Senior Project Directors and Senior Project Leadership Team to ensure alignment of Manufacturing and support functions in executing strategy. Act as Lead SME for significant quality / GMP issues. Develop, direct and maintain the local Quality System. Contribute to the development and maintenance of global quality systems in line with Lonza Corporate requirements & standards as well as current regulatory requirements meeting Swissmedic, US FDA and European requirements. Perform independent review and approval of project documents. Take part in investigations, troubleshooting, audits and inspections. Identify opportunities for optimization of operational procedures in order to improve quality and efficiency within area of responsibility. Implement a learning culture and vertical/horizontal knowledge management. What we are looking for:
Current or previous direct-line leadership experience. Agility, assertiveness and communication skills needed to excel in this highly dynamic project phase. Eligible to work as deputy for Qualified Person/FvP in Switzerland or EU and extensive work experience in a senior QA role in the GMP controlled pharmaceutical manufacturing environment (e.g., QA Operations), preferably experience in aseptic fill & finish processes. Excellent working knowledge of current ICH, PIC/S, EU and US regulatory requirements and their implementation. Experience in managing customer audits and inspections such as Swissmedic, USFDA, EMA, MHRA Audits. University degree in Life Science (Pharmacy, Biology or similar field). Fluent English and at least basic knowledge of German (plus the willingness to improve your German skills fast in case it is not fluent yet).
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An agile career and 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. Full list of global benefits: https://www.lonza.com/careers/benefits. What you will do:
Lead, develop and grow a team of QA Experts. Create and lead the overall Quality strategy. Partner with Senior Project Directors and Senior Project Leadership Team to ensure alignment of Manufacturing and support functions in executing strategy. Act as Lead SME for significant quality / GMP issues. Develop, direct and maintain the local Quality System. Contribute to the development and maintenance of global quality systems in line with Lonza Corporate requirements & standards as well as current regulatory requirements meeting Swissmedic, US FDA and European requirements. Perform independent review and approval of project documents. Take part in investigations, troubleshooting, audits and inspections. Identify opportunities for optimization of operational procedures in order to improve quality and efficiency within area of responsibility. Implement a learning culture and vertical/horizontal knowledge management. What we are looking for:
Current or previous direct-line leadership experience. Agility, assertiveness and communication skills needed to excel in this highly dynamic project phase. Eligible to work as deputy for Qualified Person/FvP in Switzerland or EU and extensive work experience in a senior QA role in the GMP controlled pharmaceutical manufacturing environment (e.g., QA Operations), preferably experience in aseptic fill & finish processes. Excellent working knowledge of current ICH, PIC/S, EU and US regulatory requirements and their implementation. Experience in managing customer audits and inspections such as Swissmedic, USFDA, EMA, MHRA Audits. University degree in Life Science (Pharmacy, Biology or similar field). Fluent English and at least basic knowledge of German (plus the willingness to improve your German skills fast in case it is not fluent yet).
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