Delegate Qualified Person Clinical Supply Quality

Johnson & Johnson Co.; Geel; On-site; EUR 70,000 - 100,000; Full time

Job summary

Johnson & Johnson is seeking a Delegate Qualified Person in R&DQA- Clinical Supply Quality to join our global clinical supply team. You will contribute to ensuring quality decisions across synthetic and biologic medicines, supporting trials and complex supply chains within a leading healthcare company.

Based in Beerse/Antwerp, Belgium, the role involves collaborating with cross-functional teams to review clinical batches, resolve quality issues, and uphold regulatory compliance for advanced

Job description

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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: Do you want your quality decisions to help innovative medicines reach clinical trial patients around the world? Are you a recognized Qualified person residing in Belgium? Join our team as a Delegate Qualified Person in R&DQA- Clinical Supply Quality. You will work at the heart of global clinical supply chains for synthetics, biotherapeutic molecules and advanced therapy medicinal products (ATMPs). Every day is different: from reviewing a clinical batch to resolving an unexpected quality issue and