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.com **Job Function:** Quality **Job Sub** **Function:** Quality Control **Job Category:** Business Enablement/Support **All Job Posting Locations:** Leiden, South Holland, Netherlands **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 "An internal pre-identified candidate for consideration has been identified. However, all applications will be considered." **We are searching for the best talent for a Quality Control Technician to be in Leiden, Netherlands!** Within the **QC-AT laboratories** of the J&J Supply Chain, the Leiden QC laboratories are responsible for release and stability testing of lentivirus produced at the various production sites of J&J. The lentivirus is tested on CAR-T% (flow-cytometry), construct copy number (qPCR) and IFNg (ELISA). **You will be responsible for:** + Perform various testing on finished products, stability samples and in-process control samples according to GMP/GLP guidelines and SOP procedures efficiently + Analyze, report and review test results to applicable systems. + General lab support functions such as ordering of lab supplies, managing generated waste, equipment handling, preparation of reagents and attending team meetings. + Identify and call out issues to supervisor in a timely manner. + Perform other work-related activities assigned by supervisor. **Qualifications/Requirements:** + Bachelor’s degree or equivalent in a relevant subject area with proven working experience in Quality Control. + Experience in cell culture, Flow-cytometry and PCR. + Can collaborate and actively work in a team environment both with internal team members and supervisors. + Profound knowledge of pharmaceutical regulations/cGMP principles (FDA, EU, etc.). + Excellent knowledge of English. Ready for the next step in your career? Apply now!#RPOAMS