QC Technician - FCT, ELISA and PCR

Technician Quality Control – Biotechnology
Leiden, Netherlands – Full-time

Company Description
A leading biotechnology company with operations in Europe and the U.S., dedicated to developing transformational medicines in oncology and immunology. With a strong pipeline of small molecules, CAR-T therapies, and biologics, the organization combines science, technology, and collaboration to address high unmet medical needs. The Leiden facility plays a central role in analytical development and quality control, ensuring products meet rigorous GMP standards and reach patients safely.

Job Description
As a Technician Quality Control, you will perform routine analytical and microbiological testing to support product release, characterization, immune monitoring, and incoming goods. You will contribute to method validation and transfers, maintain laboratory equipment, and ensure compliance with GMP practices. This role offers the opportunity to work with advanced techniques such as flow cytometry, ELISA, and PCR, while actively participating in continuous improvement initiatives within a dynamic QC environment.

Key Responsibilities

• Perform routine testing for product release, characterization, immune monitoring, incoming goods, and environmental monitoring.

• Support method transfers, validations, and qualifications.

• Provide technical support in instrument maintenance and troubleshooting.

• Ensure GMP-compliant laboratory operations and accurate documentation.

• Contribute to laboratory investigations and support deviation handling.

• Participate in continuous improvement projects within QC.

• Manage availability of reagents and consumables to ensure smooth daily operations.

• Draft and review SOPs and work instructions; act as a point of contact for lab practices.

Essential Requirements

• BSc or MSc degree in Life Sciences, Biotechnology, or related discipline.

• 1–3 years of experience in a GMP-regulated QC setting within Biotech/Pharma.

• Hands-on expertise in flow cytometry, cell-based assays, and PCR.

• Strong communication skills in English (verbal and written).

• Flexible, self-driven, and proactive mindset, with the ability to work shifts.

Desirable Experience

• Knowledge of microbiological testing methods.

• Experience drafting SOPs and supporting laboratory investigations.

• Prior exposure to LEAN/continuous improvement projects.

Additional Insights

• Location: Leiden, Netherlands

• Contract Type: Consultancy assignment with growth opportunities

• Shift Work: Required (to be introduced in the near future)

• On-site presence: 5 days per week