The Company
Our client is a global leader in healthcare innovation, committed to transforming lives through cutting-edge research, breakthrough medicines, and sustainable healthcare solutions. The organization brings together top scientific minds to discover and deliver advanced therapeutics that prevent, intercept, treat, and ultimately cure diseases. With a focus on quality, collaboration, and a world without disease, the company is shaping the future of medicine.
Role Description
As a Lab Technician GMP, you will be an essential part of the Quality Control Development (QCD) Labs team within the Analytical Development department. Your role will focus on supporting GMP activities through the execution of release and stability testing of advanced therapeutic products. You will conduct a variety of analytical and biological assays, ensure the accuracy and compliance of laboratory documentation, and maintain high standards in accordance with Good Manufacturing Practice (GMP) regulations. This is a dynamic and hands-on role that requires precision, scientific curiosity, and a strong commitment to quality in a multidisciplinary environment.
Responsibilities
- Perform GMP-compliant release and stability testing for toxicology and clinical batches of advanced therapeutics.
- Carry out assay qualifications and routine testing with a “first-time-right” mindset.
- Apply analytical and biological techniques, including UPLC/HPLC, ELISA, and PCR.
- Culture mammalian cells (e.g., A549, HEK293), including passaging and seeding.
- Document results accurately in assay run sheets, laboratory notebooks, and digital systems.
- Ensure proper use, maintenance, and qualification of laboratory equipment.
- Support the writing and updating of SOPs, test instructions, and related documentation.
- Collaborate with development teams to support process testing and improvements.
- Contribute to a high-quality working environment through precision, flexibility, and teamwork.
Requirement
- MBO or HBO degree in Life Sciences or a closely related field.
- Minimum of 2 years' experience in a GMP-regulated pharmaceutical or biotechnology laboratory.
- Strong understanding of GMP principles and experience performing assays in a regulated setting.
- Familiarity with laboratory management systems and quality documentation practices.
- Good organizational skills and a detail-oriented approach to work.
- Strong communication skills, both written and verbal.
- Fluent in English; proficiency in Dutch is a plus.
Other Information
Looking for a new opportunity in a growing and impactful field? This could be it! If you're ready to apply your laboratory skills in a meaningful and regulated environment, please click the button below to apply for the job.
56240
Similar jobs

About us
Since 2012, SIRE Life Sciences is the most innovative and engaged consultancy company for the life sciences industries.
SIRE Life Sciences is proud of its ability to adapt to changing trends while always maintaining the highest level of quality for both our clients and our candidates.
Our team of knowledgeable professionals provides customized staffing services to clients and candidates, including secondment, direct hire, temporary-to-hire, temporary staffing, brokering, Statement of Work and we approach each type with the same degree of professional assessment. Our refined and collaborative style is unmatched in the staffing industry. We’re able to see beyond the surface to create matches that result in successful careers for our candidates and valuable talent for our clients.
Effective employment solutions need to put the right person in the relevant place every time, using advanced systems to streamline costs and time-frames for clients.