Qualified Person; QP - Quality Assurance
Listed on 2026-01-09
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Quality Assurance - QA/QC
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Healthcare
Data Scientist, Medical Science
Location: Town of Belgium
Qualified Person (QP) - Quality Assurance
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About the vacancyR&D
Drug Development
Quality
Quality Control
Quality Assurance
Compliance
Regulatory Affairs
Regulatory Affairs
Regulatory compliance
Submissions
Clinical R&D
Pharmacovigilance
Engineering
Quality
Expert Bachelor’s Degree (HBO, WO) Permanent Full time Ghent, Gent, Belgium
About Your Next JobWe are looking for the best talent for a Qualified Person – Quality Assurance for the CAR‑T hub to be in Ghent Belgium!
Purpose: CAR‑T (chimeric antigen receptor T‑cell therapy) is an innovative approach to eliminate cancer cells, which work by harnessing the power of a patient’s own immune system. They are created from the patients’ own T cells and are engineered to eliminate cancer cells expressing a specific antigen.
To support the CAR‑T program in EMEA, J&J has built two CAR‑T manufacturing centers in the Ghent area (Belgium). The QC laboratories are operating from the existing J&J Beerse site. CAR‑T investigational medicinal and commercial CAR‑T products are manufactured in the Ghent facilities.
In this role, you are reporting in the J&J QA CAR‑T organization and work closely with your peers from Material Science and Technology, Operations and Quality Control.
The Qualified Person, CAR‑T Europe is responsible that product and process related investigations, complaints, batch review and release activities are accurately handled on time and in line with all ATMP/GMP requirements.
About Your Skills and ExperienceQualifications/Requirements:
- A degree in Pharmacy or Bio‑engineering is required. Certification as an Industrial Pharmacist is required (Qualified Person number).
- In‑depth understanding of pharmaceutical product development, qualification, packaging, validation, testing, release, and distribution processes.
- Regulatory Knowledge:
Up‑to‑date knowledge of pharmaceutical legislation, including current Good Manufacturing Practices (cGMP) and Advanced Therapy Medicinal (Use the "Apply for this Job" box below). analytical thinking and decision‑making abilities, with a keen attention to detail. - Excellent verbal and written communication skills to optimally negotiate and interact with both external and internal customers and partnersli>
- Proven experience working with quality systems, ensuring compliance with industry standards and regulatory requirements.
- Experience with aseptic processing and techniques is preferred, with a solid understanding of the requirements for sterile manufacturing.
- Highly organized, capable of managing multiple tasks in a team environment, and able to work optimally under minimal direction while maintaining a positive demeanour.
- Effective Communication:
Strong written and verbal communication skills in English is required. (Dutch is a plus)
Hybrid Work
You are eligible to work in EUWe only accept applicants who are eligible to work in the EU
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 Med Tech, 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.
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