For an internationally operating company in a regulated environment, we are looking for two experienced professionals in the area of Operations Compliance / Quality. In this role, you will support the laboratory organization in quality-related processes and actively contribute to ensuring GMP-compliant operations. Functieomschrijving Manage QC-related deviations, root cause investigations, CAPAs, and change controls Maintain and revise QC-specific controlled documents (e.g., test methods, SOPs, forms, logbooks) Implement CAPA within agreed timelines and support training on procedures. Support data integrity activities and ensure correct, complete, and consistent documentation Conduct or support QC-related risk assessments and mitigation activities. Monitor QC quality metrics (e.g., deviation trends, cycle times, data integrity observations) Collaborate with laboratory team leaders and QA to resolve quality issues promptly Ensure proper implementation of changes impacting QC workflows, systems, or methods Functie-eisen Several years of experience in a pharmaceutical QC environment or in a regulated laboratory Solid GMP knowledge Experience in conducting investigations and root cause analyses Very structured, reliable, and detail-oriented working style Experience with electronic quality systems and LIMS is an advantage Strong documentation and communication skills Fluent English (written and spoken); German or French is an advantage Arbeidsvoorwaarden Responsible and varied role Short decision-making paths and direct communication Collaborative environment with cross-functional teamwork Opportunity to actively shape and further develop processes