QC Analytical Lab Technician
2026-03-03
QC Analytical Associate – Up to €49,400 per year - Hoofddorp - Onsite, Shifts
Location: Hoofddorp, Netherlands
Salary: Up to €49,400 per year
Contract: 12-month contract with strong potential for extension or permanent conversion
Working Model: Full-time (40h), On-site
Shift Pattern: 16-week rotation | 3 days on, 1 day off | 9 full weekends per cycle | 10 evening shifts (12:30–21:30) | Day shifts (08:30–17:00)
Overview
Join a leading biotechnology company specializing in immunotherapy products as a QC Analytical Associate.
This position is suited for candidates with hands-on experience or that would in molecular biology and analytical testing and want to grow professionally within a regulated biotech or pharmaceutical environment.
Offer
- Salary: Up to €49,400 per year
- Contract: 12-month contract with strong potential for extension or permanent conversion
- Working Model: Full-time (40h), On-site
- Shift Pattern: 16-week rotation | 3 days on, 1 day off | 9 full weekends per cycle | 10 evening shifts (12:30–21:30) | Day shifts (08:30–17:00)
Role
As a QC Analytical Associate, you will execute analytical and molecular testing to ensure the quality, safety, and efficacy of parenteral and cell therapy products.
You'll be part of the Quality Control Analytical team supporting commercial manufacturing by performing GMP-compliant testing of raw materials, in-process samples, and final drug product.
Key Responsibilities
- Perform analytical testing of raw materials, in-process samples, and final drug product
- Execute molecular biology assays such as Flow Cytometry, ELISA, qPCR/ddPCR, and Western Blot
- Review and document test results in accordance with cGMP requirements
- Support product release testing activities
- Maintain laboratory equipment and ensure proper documentation practices
- Participate in environmental monitoring and waste management procedures
- Work in rotating shifts including evenings, weekends, and national holidays
Qualifications & Experience
- MBO or HBO degree in Analytical Chemistry, Biochemistry, Molecular Biology, or related field
- 1–3 years of QC experience in Biotech or Pharmaceutical manufacturing
- Hands-on experience with molecular and analytical testing techniques
- Strong documentation, communication, and collaboration skills
- Comfortable working in a fast-paced and changing production environment
- Willingness to work structured shift schedules
Interested?
Apply now by clicking Easy Apply with your updated CV, or feel free to contact:
Audrey Poluakan, Recruitment Consultant at Gi Life Sciences Netherlands
M: 0658069570
E: audrey.poluakan@gigroup.com
Manufacturing
Pharmaceutical And Biotechnology
5360
Amsterdam
49400
QC Analytical Associate – Up to €49,400 per year - Hoofddorp - Onsite, Shifts
Location: Hoofddorp, Netherlands
Salary: Up to €49,400 per year
Contract: 12-month contract with strong potential for extension or permanent conversion
Working Model: Full-time (40h), On-site
Shift Pattern: 16-week rotation | 3 days on, 1 day off | 9 full weekends per cycle | 10 evening shifts (12:30–21:30) | Day shifts (08:30–17:00)
Overview
Join a leading biotechnology company specializing in immunotherapy products as a QC Analytical Associate.
This position is suited for candidates with hands-on experience or that would in molecular biology and analytical testing and want to grow professionally within a regulated biotech or pharmaceutical environment.
Offer
- Salary: Up to €49,400 per year
- Contract: 12-month contract with strong potential for extension or permanent conversion
- Working Model: Full-time (40h), On-site
- Shift Pattern: 16-week rotation | 3 days on, 1 day off | 9 full weekends per cycle | 10 evening shifts (12:30–21:30) | Day shifts (08:30–17:00)
Role
As a QC Analytical Associate, you will execute analytical and molecular testing to ensure the quality, safety, and efficacy of parenteral and cell therapy products.
You'll be part of the Quality Control Analytical team supporting commercial manufacturing by performing GMP-compliant testing of raw materials, in-process samples, and final drug product.
Key Responsibilities
- Perform analytical testing of raw materials, in-process samples, and final drug product
- Execute molecular biology assays such as Flow Cytometry, ELISA, qPCR/ddPCR, and Western Blot
- Review and document test results in accordance with cGMP requirements
- Support product release testing activities
- Maintain laboratory equipment and ensure proper documentation practices
- Participate in environmental monitoring and waste management procedures
- Work in rotating shifts including evenings, weekends, and national holidays
Qualifications & Experience
- MBO or HBO degree in Analytical Chemistry, Biochemistry, Molecular Biology, or related field
- 1–3 years of QC experience in Biotech or Pharmaceutical manufacturing
- Hands-on experience with molecular and analytical testing techniques
- Strong documentation, communication, and collaboration skills
- Comfortable working in a fast-paced and changing production environment
- Willingness to work structured shift schedules
Interested?
Apply now by clicking Easy Apply with your updated CV, or feel free to contact:
Audrey Poluakan, Recruitment Consultant at Gi Life Sciences Netherlands
M: 0658069570
E: audrey.poluakan@gigroup.com

