Project Lead QC 80-100%

ppThe actual location of this job is in bStein, AG, Switzerland /b. Relocation assistance is available for eligible candidates and their families, if needed. /p pAs Project Lead Quality Control, you will act as the primary QC contact for customers, assessing laboratory capacity, coordinating analytical method transfers, thereby ensuring the successful implementation of release and stability testing for late-phase and commercial biologics. /p pWorking closely with Program Managers and cross-functional teams, you will drive QC project execution, manage timelines and customer interactions, provide scientific guidance on analytical testing strategies, and ensure regulatory and GMP-compliant delivery of project milestones. /p pThis 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. /p h3What you will get: /h3 ul liAn agile career and a dynamic work culture. /li liAn inclusive and ethical workplace. /li liCompensation programs that recognize high performance. /li liIn addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. /li /ul h3Job responsibilities /h3 ul liLead and coordinate QC related project activities for release and stability testing of late-phase (PPQ) and commercial drug products, with a focus on large molecules and Antibody Drug Conjugates (ADCs). /li liServe as the primary QC representative and project champion, driving project execution through effective coordination of timelines, deliverables, customer engagements, and stakeholder communication in close partnership with Program Managers. /li liAssess laboratory capacity and manage analytical method transfers, ensuring timely implementation of testing to meet customer and project requirements. /li liImplement analytical testing strategies, including method suitability assessments, performance evaluation, control strategies, and specification setting. /li liAuthor for quality records and cGMP documents e.g. procedures (SOPs) or source documents, reports, deviations, change requests etc. /li liAct as QC subject matter expert during audits, inspections, and customer meetings while ensuring GMP-compliant documentation and regulatory readiness. /li /ul h3What we are looking for: /h3 ul liWork experience in a GMP-regulated pharmaceutical Quality Control environment with a sound understanding of analytical testing of biologics (large molecules) is a must. /li liYou enjoy working with many different people: strong collaboration and stakeholder management skills, with the confidence to coordinate activities, provide constructive challenge, and interact effectively with customers and internal teams. /li liExperience in project coordination, analytical method validation and/or method transfer is a strong advantage. /li liFluency in English is a must, fluency in German is a plus. /li liDegree in Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, or a related life sciences discipline. /li /ul h3About Lonza /h3 pAt 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. /p pInnovation 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. /p /p #J-18808-Ljbffr