Process Engineer at Amsterdam, Noord-Holland
Details of the job offer
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-functional teams
- Solid understanding of scientific and engineering principles; strong troubleshooting mindset
- Comfortable working independently in a changing environment with shifting priorities
- Self-motivated, detail-oriented, and open to temporary responsibilities outside the initial scope
Interested?
Apply now by uploading your updated CV, and feel free to contact:
Audrey Poluakan, Recruitment Consultant at Gi Life Sciences Netherlands
M: 0658069570
E: audrey.poluakan@gigroup.com
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-functional teams
- Solid understanding of scientific and engineering principles; strong troubleshooting mindset
- Comfortable working independently in a changing environment with shifting priorities
- Self-motivated, detail-oriented, and open to temporary responsibilities outside the initial scope
Interested?
Apply now by uploading your updated CV, and feel free to contact:
Audrey Poluakan, Recruitment Consultant at Gi Life Sciences Netherlands
M: 0658069570
E: audrey.poluakan@gigroup.com