QC CAR-T Investigation Coordinator

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: About Innovative Medicine    Our   expertise   in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.   Visionaries like you work on teams that save lives by developing the medicines of tomorrow.   Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.   Learn more at https://www.jnj.com/innovative-medicine   CAR-T is an innovative treatment for blood cancer that harnesses the power of a patient’s own immune system. By genetically modifying the patient’s T-cells to recognize and eliminate cancer cells, this advanced technology offers new hope to patients for whom other therapies have provided limited or no benefit. To support the expansion of CAR-T treatment capacity in Europe, we are looking for talented and motivated colleagues to join our CAR-T hub. The Innovative Medicine Supply Chain Group, a member of the Johnson & Johnson family of companies, is recruiting a QC CAR-T Investigation Coordinator based in Beerse, Belgium.   As part of the QC team, your key responsibilities will include:   Supporting daily QC operations in close collaboration with supervisors, analysts, Production, Warehouse, and QA. Leading QC investigations and preparing final investigation reports based on thorough root cause analysis. undefined Supporting and implementing improvement projects focused on safety, quality, efficiency, and customer satisfaction. Developing and delivering training or awareness sessions within QC.

Master’s degree in biochemistry, biotechnology, or a related field; or a Bachelor’s degree with relevant experience. Knowledge of cGMP regulations and FDA/EU guidance is required. Strong organizational skills, with the ability to work independently, flexibly, and accurately. Excellent written and verbal communication skills. Professional experience in a GMP-regulated environment, preferably within Quality Control, is an advantage. Very good knowledge of Microsoft Office applications. Good knowledge of laboratory processes and systems is preferred. At a later stage, candidates must be able and willing to work in a shift schedule. Shifts may include morning and evening work, depending on clinical and commercial demand. At Johnson & Johnson, we want every candidate to feel supported throughout the hiring process. Our goal is to make the experience clear, fair, and respectful of your time. Here’s what you can expect: Application review: We’ll carefully review your CV to see how your skills and experience align with the role. Getting to know you: If there’s a good match, you’ll be invited to a short call with one of our recruitment team to understand more about you and answer any questions that you might have. Staying informed: We know waiting can be hard and processes can evolve; our recruitment team will keep you updated and make sure you know what to expect at each step.