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People in Science seeks a Process Operator for a regulated pharmaceutical production facility in Breda, Netherlands. You will operate a semi-automated production line, monitor processes, perform changeovers, and ensure GMP-compliant manufacturing with SAP/MES data logging.
The role requires extensive GMP experience, LEAN/Six Sigma knowledge, and strong troubleshooting skills (5WHY, RCA). Proficiency in Dutch and English, plus an analytical, precise work approach, are essential.
Are you an experienced Process Operator who enjoys working with advanced production equipment in a highly regulated environment? In this role, you are responsible for running a production line, monitoring the process and making sure high-quality medicines are produced safely and according to GMP procedures.
You currently work in a 3-shift schedule, with the production environment expected to transition to a 5-shift schedule around January 2027.
What will you do? You work as part of a team of experienced operators on one of several semi-automated production lines.
Your responsibilities include:
You take ownership of your production line, enjoy solving technical problems and continuously look for opportunities to improve the process.
Working hours: Full-time | Day shift (no shift work) Work location: On-site, 100% Start date: As soon as possible About the Company Our client is a leading international biotechnology compan …