Quality Assurance Associate – Delegate Qualified Person at Johnson & Johnson in Antwerp

Job description

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. Learn more at jnj.com . As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Quality Job Sub Function: Quality Assurance Job Category: Professional All Job Posting Locations: Beerse, Antwerp, Belgium Job Description: Quality Assurance Associate – Delegate Qualified Person Do you want to develop your quality expertise while helping innovative medicines reach clinical trial patients around the world? Are you a recognized Qualified Person residing in Belgium and looking to build your experience? Join our team as a Quality Assurance Associate- Delegate Qualified Person in R&DQA- Clinical Supply Quality. You will work with experienced colleagues across global clinical supply chains for synthetics, biotherapeutic molecules and advanced therapy medicinal products (ATMPs). From reviewing clinical batch documentation to supporting quality investigations and process improvements, your work will help enable safe, compliant and timely delivery to clinical trials. You will build your QA and Delegate QP experience with support from experienced colleagues, taking on broader responsibilities in line with your training and authorization. You will broaden your knowledge of products, technologies and regulations while collaborating with colleagues worldwide. Ready to bring quality closer to patients? Apply today. What you can expect from this role Meaningful impact: help clinical trial materials reach patients safely and on time, supporting medicines as they progress towards commercialization. You will gain experience in a dynamic, fast-paced environment where adaptability and practical thinking are valued. Learning and development: gain hands-on exposure to different products, technologies, supply chains and worldwide regulatory expectations. Growing responsibility: develop your quality judgement, contribute to investigations and put improvements into practice with guidance from experienced colleagues. Global collaboration: work with multidisciplinary teams and external partners across Europe and the US. Exposure and growth: build your quality expertise, learn from colleagues and support preparation for audits and Health Authority inspections. Develop an understanding of the end-to-end product supply chain. Contribute fresh ideas: ask questions, identify opportunities to improve existing processes and help turn ideas into practical solutions. Learn in an innovative environment: explore how quality processes evolve to support new technologies and contribute to their development alongside experienced team members. What you will do Connect with the right experts: work with Clinical Supply Chain teams and global quality partners, including J&J (pilot) plants, ECSQ, Quality Asset Management to gather and follow up the information needed for timely release and QP certification. Support quality from the start: contribute to cross-functional teams alongside experienced Clinical Supply Quality colleagues and help incorporate quality requirements into clinical trial execution. Support release of clinical trial materials: review batch information and perform assigned release activities within the Janssen R&D IMP license, following appropriate training and authorization. Build towards broader Delegate QP respo