Process Engineer at Amsterdam, Noord-Holland

Details of the job offer

  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-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



  Manufacturing
  Pharmaceutical and biotechnology
  8142
  58230
Process Engineer
Temporary / Amsterdam
Place of work - City:
Amsterdam
Industrial sector:
Manufacturing
Professional area:
Pharmaceutical and biotechnology
Number of vacancies:
1
Reference code:
6722
Salaris:
58230
Salaris tot:
58230
Salaris per:
Job offer insertion date:
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-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




https://nl.gigroup.com/job-detail/amsterdam-noord-holland-process-engineer/6722/