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:** Non-Standard **Job Sub** **Function:** Workday Associate B **Job Category:** Non-Standard **All Job Posting Locations:** Beerse, Antwerp, Belgium **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 **​** **We are searching for the best talent for a** **Quality Control Analyst in the weekend shift to join our CAR-T** **Hub located** **in Beerse.** 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/ . CAR-T (chimeric antigen receptor T-cell therapy) is an innovative approach to eliminate cancer cells, which work by harnessing the power of a patient’s own immune system. They are created from the patients’ own T cells and are engineered to eliminate cancer cells expressing a specific antigen. To support the CAR-T program in EMEA, Janssen has built two CAR-T manufacturing centers in the Ghent area (Belgium). The QC laboratories will be operated from the existing Janssen Beerse site. The QC Biotech analyst, CAR-T Europe is responsible for preparing and conducting testing of the different samples taken during the production process. You are responsible for ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations. **You will be responsible for:** + Perform analytical testing in compliance with all applicable specifications, procedures, GMP regulations + Maintain a safe work environment in compliance with all applicable environmental, health and safety regulations + Perform peer review of laboratory data author and update SOPs, Wis and Protocols to support daily operations of the lab using the document management system + Support laboratory related invetigation records and CAPAs + Assist in the execution of internal audits and provide input to functional laboratory meetings + Provide input and tak actions as a QC representative at cross-laboratory meetings SHE responsibilities: + Always strictly apply all applicable prevention rules and procedures + Make correct use of the personal and collective protective equipment provided, process and system ownership, ensuring order and tidiness + Reporting (near) accidents, incidents, deviations and risky situations + Conributing to and proposing solutions to improve safety, health and the environment + Addressing other employees and third parties when prevention procedures are not followed or when unsafe behavior is reported **Qualification and requirements:** + A minimum of a bachelor’s degree in a Scientific or related field is required + A minimum of two (2) years of experience working in a cGMP compliant QC laboratory or equivalent is required. + Understanding of analytical data generated from performing biological and biochemical analytical techniques is required. + Detailed knowledge of analytical technologies used in the QC laboratory (CAR-T experience) is required. + Experience in performing cellular and/or molecular based techniques such as qPCR, Flow, Cytometry and/of Potency assays is required. + Basic, kwowledge of compendial (USP, EP, JP, etc.) requirements pertaining to their functional area of QC is preferred. + Proficient with using Microsoft Office applications (Outlook, Excel, Word, and Powerpoint) is required. Systems: eLims -SAP -Truvault -Summit 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 youthrough 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