Mark this as favouriteQC Lab Tech II Analytical

Analytical Laboratory Technician – Quality Control | Up to €49,495 per year | Hoofddorp

Looking for a QC analytical role with strong qPCR exposure?

Join a leading biotechnology and pharmaceutical organization in Hoofddorp and play a key role in ensuring the quality of advanced therapeutic products, with a strong focus on qPCR-based testing.

As an Analytical Laboratory Technician, you’ll be part of the QC Analytical team, performing molecular and analytical testing—particularly qPCR assays—on raw materials and final products to support manufacturing, release, and patient safety.

Offer

• Salary: Up to €49,495 per year
• Location: Hoofddorp, North Holland, Netherlands
• Employment Type: Full-time | Onsite
• Working Hours: Monday–Friday, 08:30–17:00 (no weekends)
• Contract: Initial 12-month temporary contract with high likelihood of extension or conversion to permanent
• Environment: GMP-regulated QC laboratories working with advanced therapies

Your Role

In this role, you’ll support the QC Analytical group by executing high-quality qPCR and molecular biology testing on raw material and final product samples.

Given the complexity of the products, this position requires strong ownership of analytical processes, excellent aseptic technique, and a high level of data accuracy in a regulated laboratory environment.

Key Responsibilities

• Perform qPCR-based analytical testing on raw material, in-process, and final product samples
• Execute molecular biology assays such as qPCR, ddPCR, and related techniques in a GMP environment
• Review, evaluate, and document qPCR and analytical test results in compliance with GMP requirements
• Ensure correct execution of assay controls, standards, and data integrity checks
• Support routine maintenance and qualification of laboratory equipment used for qPCR analysis
• Follow approved SOPs, cGMP, and safety procedures at all times
• Participate in waste management and general laboratory support activities
• Contribute to a compliant, inspection-ready QC analytical environment

Qualifications & Experience

• MBO or HBO degree in Analytical (Bio)Chemistry, Molecular Biology, or a related field
• 1–3 years of QC experience in the biotech and/or pharmaceutical industry preferred
• Strong hands-on experience with qPCR assays is required
• Experience with ddPCR, Western blotting, or cell therapy-related analytics is a strong plus
• Working knowledge of cGMP, GLP, and regulatory requirements for analytical testing is preferred
• Strong English communication skills (verbal and written)
• Detail-oriented, quality-focused, and comfortable working in a fast-paced QC environment

Interested?

Apply today 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