QA associate - QA Lab at Johnson & Johnson in Geel, Flanders, Belgium

QA associate - QA Lab Location: Geel, Antwerp, Belgium 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: Geel, Antwerp, Belgium Job Description: Within J&J Innovative Medicine Supply Chain, a member of the Johnson & Johnson Family of Companies, we are currently recruiting a QA Associate – QA Lab to join our Quality team in Geel, Belgium. The Geel site serves as a Center of Excellence for the development and manufacturing of Small Molecule Active Pharmaceutical Ingredients (SM-API) and Drug Product (DP) Intermediates, supporting therapies that improve the health and lives of patients worldwide. Within Innovative Medicine Supply Chain Quality (IMSCQ), we ensure robust quality oversight and enable reliable product supply in full compliance with global regulatory requirements. Role Overview As QA Associate – QA Lab, you will provide quality oversight of the Quality Control (QC) laboratories, supporting activities related to the testing of: Final APIs and intermediates Raw and packaging materials Drug product intermediates Cleaning validation You will act as a key QA partner to QC laboratories, ensuring compliance, driving continuous improvement, and safeguarding patient safety and product quality. Key Responsibilities Act as QA Point of Contact for QC laboratories, ensuring alignment with global regulations and internal standards Provide QA review and approval for GMP documentation supporting laboratory operations Support investigation of laboratory deviations, including: Root cause identification Review and approval of investigation reports Definition and follow-up of CAPAs Trending and continuous improvement actions Provide QA oversight on analytical method transfers and implementation Ensure timely and compliant handling of quality records (deviations, CAPAs, change controls, method transfer documentation) Drive process improvements and foster a culture of innovation and quality excellence Act as SME and spokesperson during health authority inspections and customer audits Ensure proper escalation of issues with potential impact on patient safety or product supply Profile & Qualifications Master’s degree in a scientific field (analytics, chemistry, biotechnology or equivalent experience) Minimum 5 years of experience in QC and/or QA within the pharmaceutical, chemical or food industry At least 4 years in an analytical environment Strong knowledge of cGMP, ICH guidelines, and regulatory expectations Proven ability to make risk-based, data-driven decisions Strong analytical thinking and problem-solving skills Experience with analytical troubleshooting and investigation processes Proven ability to work independently, manage multiple priorities, and collaborate cross-functionally Strong communication and stakeholder management skills Fluent in Dutch and English This role operates under a hybrid working model; however, due to the nature of the position, a strong onsite presence is preferred. Team members coordinate schedules to ensure continuous onsite coverage, and flexibility is expected to support this requirement. What We Offer At Johnson & Johnson, we are committed to supporting the whole health of our employees—physically, emotionally and professionally—while offering opportunities to grow in a dynamic, global environment. Required Skills: Preferred Skills: Business Alignment, Business Behavior, Coaching, Compliance Management, Continuous Improvement, Data Analysis, Detail-Oriented, Goal Attainment, Human-Centered Design, Internal Controls, Issue Escalation, Problem Solving, Process Oriented, Quality Control (QC), Quality Management Systems (QMS), Quality Standards The anticipated base pay range for this position is: €60 000,00 - €96 255,00 Benefits: In addition to base pay, we offer the following benefits*: an annual bonus with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees’ and companies’ performance of the previous calendar year, or sales commissions. Moreover, we offer vacation days, parental leave for a minimum of 12 weeks, bereavement leave, caregiver leave, volunteer leave, well-being reimbursement, programs for financial, physical and mental health. We also offer service anniversary and recognition awards, and subject to the terms of their respective plans, employees - and in some location’s eligible dependents - can participate in several insurance plans. For more information, visit Employee benefits | Supporting well-being & career growth | Johnson & Johnson Careers. *This is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change.