Ph3Location /h3 pStein, AG, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. /p h3About the Role /h3 pJoin our Drug Product Services team in Stein, Switzerland – a leading CDMO branch shaping the future of patient treatment. As a Quality Assurance Expert Manufacturing Release, you’ll play a key role in the release of drug product from our aseptic fill‑finish lines, ensuring product quality requirements are met while providing rigorous oversight from technical transfer, manufacturing and release. This role is fully site‑based, supporting close real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. The position is part‑time at 60%. /p h3What You Will Get /h3 ul liAgile career and a dynamic work culture. /li liInclusive and ethical workplace. /li liCompensation programs that recognize high performance. /li liCompetitive salary and numerous lifestyle, family and leisure benefits. /li liFull list of our global benefits: /li /ul h3What You Will Do /h3 ul liPerform batch release for aseptic manufactured drug product. /li liWrite, review and approve deliverables (e.g., procedures, SOPs, risk assessments, gap assessments) and related databases (e.g., training, validation) to ensure GMP compliance. /li liReview and approve documents in both electronic systems (e.g., MES) and paper‑based. Approve change requests, deviation and CAPAs related to product and process. /li liPromote and enforce compliance to internal and external guidelines regarding quality and safety. /li liEnsure required knowledge and skills, identify competency gaps, and develop solutions. Lead development and evaluation of new tools, processes, quality initiatives and plans. /li liBe present at the manufacturing line to observe and support manufacturing‑related activities. /li liSupport projects and maintain Sterile Production Stein line functions in GMP compliance related issues. /li /ul h3What We Are Looking For /h3 ul liDegree (BSc, MSc or PhD) in Natural Sciences, Pharmaceutical Sciences or related field. /li liWork experience in sterile drug product manufacturing or sterile drug substance manufacturing in a GMP controlled environment. /li liExperience in deviation and change management is a prerequisite. /li liExperience in QA is an advantage. /li liHands‑on personality, open approach to business partners, excellent influencing and negotiation skills. /li liFluency in English required, German language skills advantage. /li /ul h3About Lonza /h3 pAt Lonza, our people are our greatest strength. With over 30 sites across five continents, our globally connected teams manufacture medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. We value diversity and create inclusive environments. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board. /p h3Ready to shape the future of life sciences? Apply now. /h3 pReference: R76523 /p /p #J-18808-Ljbffr