Process Engineer MSAT at Haarlemmermeer, Noord-Holland

Process Engineer MSAT – Salary of €58,320 per year – Biotech & Pharmaceutical Industry - Netherlands

Looking for a hands-on manufacturing support role where your technical expertise directly impacts patient outcomes?

Join a leading Biotechnology and Pharmaceutical company in Hoofddorp and support the commercial production of T‑cell therapy products for cancer patients worldwide.

Your Role

As a Process Engineer, you’ll join the Manufacturing Operations and Compliance Support team, tasked with providing technical support to operations, performing impact assessments supporting product release, leading root-cause investigations, driving continuous improvement, and supporting site projects in a regulated cGMP environment.

Offer

• Salary: Up to €58,320 per year (based on 40 hours)
• Location: Hoofddorp, North Holland, Netherlands
• Work Model: Full-time (40h/week) | Onsite
• Contract Type: Initial 12-month temporary contract with possibility of extension or conversion
• Working Environment: Commercial cell therapy manufacturing site (cGMP-regulated)

Key Responsibilities

• Collaborate with technical and operational stakeholders to support day-to-day manufacturing and compliance needs
• Write, review, and revise SOPs, batch records, and other operations-related documentation
• Lead and coordinate deviation investigations, applying structured Root-Cause Analysis methodologies
• Define, implement, and document CAPAs to address root causes and verify effectiveness
• Support impact assessments linked to product release activities
• Contribute to continuous improvement initiatives and site projects as assigned by management

Qualifications & Experience

• Minimum of BSc in Biochemical Engineering, Chemical Engineering, Biotechnology, or equivalent (an Engineering degree is a strong plus)
• Prior experience in cell culture, cell therapy, and/or aseptic processing
• Strong working knowledge of cGMP and experience with deviations, change controls, investigation reports, and corrective actions
• Proven ability to work cross-functionally and communicate clearly with diverse stakeholders
• Solid understanding of scientific and engineering fundamentals applied to manufacturing
• Comfortable in a fast-paced, scaling environment with shifting priorities
• Able to work independently, troubleshoot effectively, and maintain high attention to detail
• Self-driven, flexible, and willing to take on temporary responsibilities beyond the initial scope

Interested?

Apply now by submitting your updated CV, or reach out to:

Sari Steenhauer, Team Lead Life Sciences at Gi Life Sciences Netherlands

M: 0633137746

E: sari.steenhauer@gigroup.com