For a global player in the pharmaceutical industry, we are looking for an experienced QC officer with experience in stability of active pharmaceutical ingredients. The position is under GMP-regulations and offers a broad set of diverse tasks. Job description This international pharmaceutical company continuously tests their products on various aspects to maintain high quality standards, primarily using (liquid) chromatography. As a QC officer in the you are responsible for validation and compliance within the stability department. Mostly you will work with HPLC, GC, and QA tasks like management of CAPA's, deviations, Out of specifications and changes. Responsibilities Stability testing of Active pharmaceutical ingredients with HPLC and GC Validation of laboratory equipment QA tasks like change- and deviation management, CAPA's and OOS Troubleshooting of laboratory equipment Profile BSc degree (HBO) or MSc degree with additional practical working experience Strong knowledge of HPLC Experience working in a GMP-regulated environment Experience working with trackwise is a pre Communicatively strong in English, both written and spoken Benefits Long term, initially a contract through Oxford for ⚠ months Salary range: €⚠,- to €⚠,- gross per month Fulltime position: ⚠h/week Travel costs are reimbursed Region: Haarlem Vacaturenummer: ⚠ IMPORTANT NOTE : Please do not apply if you do not have a working permit to live and work in the Netherlands. Your application will not be processed.