QC Micro analist weekend
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What you'll do
- 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.
What they're looking for
- 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.
Nice to have
- Knowledge of compendial requirements (USP, EP, JP) is preferred.
- Proficiency in Microsoft Office applications (Outlook, Excel, Word, and PowerPoint).
- Prior CAR-T, cell therapy, or biopharmaceutical experience is highly desirable.
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
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-StandardJob Sub Function:
Workday Associate BJob Category:
Non-StandardAll Job Posting Locations:
Beerse, Antwerp, BelgiumJob 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.
Key Responsibilities
- 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.
Requirements
- 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: 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 #SCQuality
Required Skills:
Preferred Skills:
The anticipated pay range for this position, in the primary posting location, is:
€0,00 - €0,00
The anticipated pay ranges for additional locations are:
Belgium – The anticipated base pay range for this position is EUR 43435.00 - EUR 58765
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.
Company
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