Cell Culture Lab Technician

SIRE LIFE SCIENCES; Leiden; On-site; EUR 40.000 - 60.000; Full time

Job summary

A leading pharmaceutical company in Leiden is seeking a Cell Culture Lab Technician to support quality control in the development of advanced therapeutic products. The ideal candidate will have at least 2 years of experience in a GMP environment, a relevant degree, and strong analytical skills. Responsibilities include conducting testing, maintaining documentation, and managing laboratory operations. Join our team to make a difference in healthcare innovation.

Qualifications

• Minimum of 2 years experience in a pharmaceutical or GMP-regulated environment.
• Strong familiarity with GMP standards and laboratory management systems.
• Detail-oriented and flexible, committed to high-quality work.

Responsibilities

• Conduct release and stability testing for GMP/TOX and clinical batches.
• Perform routine analytical and biological assays.
• Maintain accurate documentation and handle cell culture tasks.

Skills

Analytical testing

Biological testing

Attention to detail

Effective communication

Education

MBO or HBO degree in life sciences

Tools

UPLC/HPLC

ELISA

PCR

Job description

Overview

The client is the pharmaceutical division of a global FMCG, focused on transforming healthcare by advancing science to prevent, treat, and cure complex diseases. The organization drives innovation in areas such as oncology, immunology, neuroscience, and advanced therapeutics, combining cutting-edge research with strategic collaborations to deliver impactful solutions.

Role Description As a Cell Culture Lab Technician within the Quality Control Development group of the Analytical Development department, you will play a key role in supporting the development and production of advanced therapeutic products. You’ll be part of a multidisciplinary team focused on ensuring the quality and reliability of laboratory and production processes, the company’s mission to transform lives through innovative medicine.

Responsibilities

• Conducting release and stability testing for GMP/TOX and clinical batches of advanced therapeutics.
• Performing routine analytical and biological assays such as UPLC/HPLC, ELISA, and PCR with precision and consistency.
• Supporting assay qualification activities in GMP laboratories.
• Maintaining accurate documentation including assay run sheets, lab notebooks, and equipment logs.
• Handling cell culture tasks including passaging and seeding (e.g., A549, HEK293).
• Assisting in process development testing and coordinating outsourcing activities.
• Managing incoming materials and chemicals, ensuring proper inspection, storage, and handling.
• Monitoring cleanroom environments and production utilities to maintain controlled conditions.
• Ensuring laboratory equipment is qualified, available, and properly maintained.
• Drafting and revising technical documents such as test and work instructions.

Qualifications

• MBO or HBO degree in a life sciences discipline.
• At least 2 years of experience in a pharmaceutical or GMP-regulated environment.
• Strong familiarity with GMP standards and laboratory management systems.
• Skilled in analytical and biological testing methods.
• Detail-oriented, flexible, and committed to high-quality work.
• Effective communicator in English (and preferably Dutch), both written and verbal.
• Positive, proactive mindset with strong interpersonal skills.

Other information

Apply to our vacancy for more information. Looking forward to getting in touch!