QA lab associate IPL

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 https://www.jnj.comJob FunctionQualityJob Sub FunctionQuality AssuranceJob CategoryProfessionalAll Job Posting Locations:Gent, East Flanders, BelgiumJob DescriptionAbout Innovative MedicineOur 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-medicineWe are searching for the best talent for QA lab associate IPL to be based in Gent! This role focuses on ensuring IPL laboratory compliance, with accurate and timely review of investigations and careful analysis of QC data to identify trends that can drive quality improvements. You’ll be part of a collaborative quality team that partners across functions to strengthen regulatory readiness and continuous improvement. This is a role that values initiative, learning, and contributing to a culture of safety and quality!As a QA Lab Associate IPL, You WillProvide compliance oversight for the IPL laboratories, ensuring accurate and timely review of laboratory investigations, performing analysis on quality indicating data and identifying any trends noted for QC data.Support drafting and approving of standard operating procedures.Perform spot-checks in the IPL Lab to ensure compliance with written regulations, policies, procedures, and global procedures.Ensure non-conformances are investigated thoroughly and approved in a timely manner and appropriate corrective and preventive action plans are implemented.Strive to reduce non-conformances in supported areas by proactively driving compliance.Provide compliance oversight for analytical instrument qualification.Qualifications/RequirementsA minimum of a Master Degree in Engineering, Science or equivalent technical discipline.A minimum of 2 years of experience in Quality Assurance.Knowledge of cGMP regulations.Knowledge of FDA/EU guidance.Experience in biotechnology methods like flow cytometry.Experience with cell counting and viability.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. Final steps: For successful candidates, you will need to complete country-specific checks before starting your new role. We will help guide you through these.  Finally, at the end of the process, we’ll invite you to share feedback in a short survey — your input helps us continue improving the experience for future candidates. Thank you for considering a career with Johnson & Johnson. We’re excited to learn more about you and wish you the best of luck in the process! #RPOEMEA