GMP Officer (QC)

ppAre you an experienced quality compliance specialist in analytical chemistry looking to make a direct impact on life‑saving biopharmaceutical products? Join our Quality Control team in Basel to drive critical laboratory compliance, deviation investigations, and root‑cause analyses. /p h3Fully site‑based roles /h3 pThis is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. /p pbStart date: /bAs soon as possible /p pbContract: /b Duration: 12 months /p pbHours: /b 41 hours per week /p h3What you will get: /h3 ul liAn agile career and dynamic working culture. /li liAn inclusive and ethical workplace. /li liCompetitive hourly rate. /li /ul pCompensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge. /p h3What you will do: /h3 ul liDrive compliance and operational excellence within our Quality Control analytical laboratories supporting biopharmaceutical manufacturing. /li liLead end‑to‑end deviation investigations, root‑cause analysis (RCA) and author comprehensive Corrective and Preventive Action (CAPA) plans. /li liWrite, review and manage Quality Change Requests and associated quality‑relevant documentation to meet tight submission timelines. /li liAct as a key compliance bridge between Quality Control (QC) analytical teams and central Quality Assurance (QA) stakeholders. /li liPartner directly with lab technicians, conducting interviews and gathering analytical data across physico‑chemical and bioanalytical workflows. /li liSupport compliance activities related to sample management processes and analytical instrument qualification protocols. /li liFoster continuous process improvement within the QC track systems and mentor lab staff on data integrity standards. /li /ul h3What we are looking for: /h3 ul liMinimum 5 years of practical experience within analytical chemistry, bioanalytics or a GMP laboratory environment. /li liProven expertise in authoring quality‑relevant records, managing deviations, OOX investigations and CAPA implementation. /li liStrong practical knowledge of GMP principles, analytical methods, data integrity, instrument qualification and sample management. /li liDemonstrated hands‑on experience performing structured root‑cause analysis techniques in a laboratory setting. /li liEducational background with a Bachelor's degree (BSc required; MSc or PhD preferred) in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related discipline. /li liProfessional business fluency in English (written and spoken) is required; basic German language skills are an advantage. /li liExcellent interpersonal and communication skills to effectively collaborate with lab personnel and align with QA decision‑makers. /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. /p pAs Lonza’s talent acquisition partner, please note, Randstad is responsible for the engagement and contracting of this contingent role. /p /p #J-18808-Ljbffr