QC Micro analist weekend

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: 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   Job Description The QC Micro Analyst, CAR-T Europe is responsible for preparing, performing, and reviewing microbiological testing activities that support the production of CAR-T therapies. Working within a cGMP-compliant Quality Control laboratory, the analyst ensures that all testing is conducted in accordance with approved procedures, regulatory requirements, and quality standards. The role supports laboratory operations through microbiological analysis, documentation management, investigations, audits, and cross-functional collaboration, while maintaining a strong focus on data integrity, compliance, and patient safety. This position is part of the weekend team, working Saturday and Sunday from 6:00 AM to 6:00 PM.

Perform microbiological testing and analytical activities in compliance with GMP regulations, approved procedures, and quality specifications. Review laboratory data to ensure accuracy, completeness, compliance, and data integrity. Author, revise, and maintain SOPs, Work Instructions (WIs), and laboratory protocols within the document management system. Support laboratory investigations, deviations, CAPAs, and other quality-related activities. Assist with internal audits and maintain inspection readiness within the QC Microbiology laboratory. Participate in laboratory and cross-functional meetings, providing technical input and representing the QC team when required.

Bachelor's degree in a Scientific discipline or a related field. Minimum of 2 years of experience in a cGMP-compliant Quality Control laboratory or a similar regulated environment. Strong understanding of microbiological testing principles and interpretation of microbiological data. Experience with microbiological laboratory techniques, including aseptic practices, endotoxin testing, growth promotion testing, sterility testing, and environmental monitoring. Knowledge of compendial requirements (USP, EP, JP) is preferred, along with proficiency in Microsoft Office applications (Outlook, Excel, Word, and PowerPoint). Excellent written and verbal communication skills; prior CAR-T, cell therapy, or biopharmaceutical experience is highly desirable. 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: