Keywords
- BSc. / HBO
- GMP
- Cell Culture
- Analytical assays (HPLC, UPLC)
- Biological assays (Elisa, PCR)
Profile
Are you a motivated lab technician who thrives in a multidisciplinary environment? The QCD Lab at JNJ Innovative Medicine is looking for a candidate who enjoys working with advanced therapeutic products and contribute to high-quality, GMP-compliant testing.
As part of the Release and Stability team, you will be responsible for performing routine and qualification assays on GMP, TOX, and clinical batches. You’ll work with precision and a “first time right” mindset, using techniques such as UPLC/HPLC, ELISA, and PCR. Your role also includes accurate documentation, supporting process development testing, and culturing cell lines like A549 and HEK293. Additionally, you’ll contribute to writing and updating lab instructions and protocols, ensuring the standards remain high and consistent.
Who we're looking for
You have a background in Life Sciences (MBO or HBO level) and bring at least two years of experience in a pharmaceutical environment. You’re familiar with working under GMP conditions and have a strong affinity for executing assays with precision and care. You have experience with analytical and biological assays like HPLC, PCR and ELISA. Your experience with laboratory management systems, combined with your flexible and accurate working style, makes you a reliable team member. With well-developed interpersonal skills and a positive, can-do attitude, you communicate effectively in English (and preferably also in Dutch), and enjoy building strong professional relationships.
Department
The Quality Control Development (QCD) group within the Analytical Development (AD) Department of the Advanced Therapeutics AD sector of J&J Innovative medicine.
The QCD Labs group focuses on supporting production and laboratory activities with:
- Inspection, release and change management of incoming production raw materials and laboratory chemicals.
- Sample and Material receipt, handling, storage and forwarding.
- Maintaining controlled state of production clean room and production utilities by environmental and utility monitoring programs.
- Coordination of Release and Stability testing and Outsourcing Coordination.
- Internal release and stability testing including culturing of cells.
- Ensuring the availability and maintenance of qualified equipment used in the laboratories.
Company profile
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Additional vacancy information
Reference | : | A2500055 |
Contract | : | Temporary contract with CLS Services |
Education | : | HBO/BSc.
MBO |
Employment terms | : | Contract for at least one year. Salary: 37000 - 43000 Days of leave: 36 See here our other employment terms for this vacancy |
Publication date | : | 7-10-2025 |
Location | : | View location with Google Maps |
Contactperson | : | Claudia Erwich-Faaij |
| | +31 (0)88 22 77 555 |
CLS Services is a leading professional recruitment agency, specialised in the recruitment and secondment of people with a background in chemistry & life sciences.