GMP Officer (QC - 7099)

ppbCTC /b is a specialized search and recruitment partner for the Life Sciences industry, serving clients and candidates since 1997. We enable careers by connecting talented professionals with meaningful opportunities, and we support our clients in engaging, retaining, and developing the right talent when needed. /p pOur client, a global market leader in the production and process support of active pharmaceutical ingredients, both in the chemical and biotechnology sectors, is looking for a: /p h3GMP Officer (QC) /h3 pon a 12-month contract, with possibilities of extension. This role is based in Basel, Switzerland, and requires work-onsite 5 days per week. /p h3Main responsibilities: /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 h3Qualifications and Experience: /h3 ul liRelevant working/residency permit or Swiss/EU-Citizenship required. /li liEducational background with a Bachelor's degree (BSc required; MSc or PhD preferred) in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related discipline. /li 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 liProfessional business fluency in English (written and spoken) is required; basic German language skills are an advantage. /li /ul /p #J-18808-Ljbffr