GMP Process Technician - Cell Therapy Manufacturing

Bristol Myers Squibb; Leiden; On-site; EUR 60,000 - 78,000; Full time

Job summary

Bristol Myers Squibb Netherlands is seeking a Specialist Process Technician to maintain, install and troubleshoot GMP process equipment at our Leiden production site. This on-site, 24/7 role focuses on minimizing production impact while complying with cGMPs, with hands-on, safety‑driven work.

You will join a team dedicated to cell therapy manufacturing, participate in training, ensure proper documentation in CMMS, and collaborate with manufacturing, facilities and vendors to keep equipment

Qualifications

• MBO level 4 diploma or equivalent; technical degree preferred.
• Proficiency in reading and writing English.
• 3+ years maintenance experience, preferably with process/lab equipment.
• Direct GMP facility experience and GMP record-keeping.
• Troubleshooting electro-mechanical systems and lab equipment.
• Willingness to work later shifts and on-call duties.
• Strong attention to detail and adherence to safety.
• Experience with CMMS and documentation practices.
• Self-motivated with minimal supervision.
• Excellent written and verbal English.

Responsibilities

• Perform maintenance, installation and troubleshooting of GMP process equipment.
• Ensure documentation stored in CMMS and compliant with GxP.
• Participate in training to expand maintenance knowledge.
• Review SOPs or job plans and assist.
• Provide basic troubleshooting of clean utilities and equipment.
• On-call duty and possible overtime/weekend hours.
• Coordinate with F&E, Manufacturing, Warehouse and Vendors.
• Daily contact with supervisory staff for assignments and coaching.

Skills

English proficiency

On-call readiness

Education

MBO level 4 diploma

Technical degree preferred

Tools

CMMS

Document Management Systems

GxP documentation practices

Job description

Bristol Myers Squibb Netherlands is seeking a Specialist Process Technician to maintain, install and troubleshoot GMP process equipment at our Leiden production site. This on-site, 24/7 role focuses on minimizing production impact while complying with cGMPs, with hands-on, safety‑driven work.

You will join a team dedicated to cell therapy manufacturing, participate in training, ensure proper documentation in CMMS, and collaborate with manufacturing, facilities and vendors to keep equipment