About this role
2026-07-16 Salary: €58230/year Contract: Temporary contract for 12 months, with a possibility of extension Location: Hoofddorp, Hybrid 2 days WFH Full-time, 40h/week As a Process Engineer you will join the Manufacturing Operations & Compliance Support (MOCS) team within MSAT at our client's cell therapy manufacturing site in the Netherlands. You'll support product release readiness, drive deviation investigations, and deliver continuous improvement in a fast-paced, highly regulated cGMP environment producing T-cell therapy products. What we offer - Competitive salary - 25 vacation days (based on full-time) - Travel allowance / commuting support - Pension scheme - Training budget and growth in MSAT, compliance, and bioprocess engineering - Agency support throughout the recruitment process and onboarding with the client What you'll do - Perform impact assessments that support batch disposition / product release and operational decision-making - Collaborate with technical and operational stakeholders across Manufacturing, QA, QC, MSAT and Supply Chain - Write and revise SOPs, batch records, and other GMP manufacturing documentation - Lead and coordinate deviation investigations, using structured Root Cause Analysis tools - Define, implement and track CAPAs to address root cause and verify effectiveness - Support continuous improvement initiatives and cross-functional projects within Manufacturing Operations - Take on additional tasks as assigned by management in line with site priorities What you bring - BSc in Biochemical Engineering, Chemical Engineering, Biotechnology or equivalent (Engineering degree is a strong plus) - Experience in cell culture, cell therapy, and/or aseptic processing in a manufacturing setting - Strong knowledge of cGMP compliance with hands-on experience in deviations, investigation reports, change controls, and corrective actions - Clear communication skills and proven ability to work in cross-functiona...