QA Release Responsible Incoming Materials & EU Release

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: QA Release Responsible Incoming Materials & EU Release   Job Description We are looking for a quality-driven professional who thrives in a dynamic pharmaceutical manufacturing environment and is passionate about ensuring patient safety, product quality and regulatory compliance. You enjoy collaborating with cross-functional teams, building strong partnerships and making sound quality decisions in a fast-paced setting. At the J&J Innovative Medicines Supply Chain (IM SC) Beerse site, a wide range of pharmaceutical products are manufactured, packaged and distributed worldwide. The Site Quality organization ensures that all GMP-related activities are performed in compliance with applicable regulatory requirements and company standards.   Within the Quality organization, the QA Release team is responsible for the quality oversight and release of incoming materials, including raw materials and packaging materials, as well as supporting EU Batch Release activities for finished medicinal products. As a QA Release Responsible, you play a critical role in safeguarding product quality and maintaining continuity of supply. You are responsible for the timely and compliant release of raw materials, excipients and packaging materials for manufacturing operations. In addition, you support EU Release activities by ensuring that all quality requirements have been fulfilled before products are certified and released to the market.   You provide quality oversight, assess quality-related events, and collaborate closely with QC, planning,…. Through risk-based decision making and strong stakeholder engagement, you ensure compliance while balancing patient safety and business continuity.

Provide QA oversight for Deviations, CAPAs, Change Controls, Complaints and trend investigations related to incoming materials or batch release activities. Ensure investigations are conducted in a timely, scientific and compliant manner and effectively address root causes. Review and approve GMP documentation in accordance with applicable procedures and regulations. Partner with QC laboratories, Manufacturing, Procurement, Supply Chain and external suppliers to ensure alignment and timely resolution of quality issues. Establish and maintain strong working relationships with Business and Quality partners to ensure alignment of objectives and results and act as Quality Point of Contact Drive continuous improvement initiatives to strengthen quality systems and operational excellence. Participate in cross-functional governance meetings and represent Quality in project teams. Support Health Authority inspections and customer audits as a subject matter expert for incoming material release and EU release processes. Ensure inspection readiness through strong GMP compliance and effective quality oversight. Promote a proactive quality culture focused on patient safety, compliance and continuous improvement.   Material Release Review and approve the release of raw materials,