QC Micro analist weekend

jj; Beerse; Sur place; EUR 55 000 - 74 000; Plein temps

Résumé du poste

Johnson & Johnson is seeking a QC Micro Analyst, CAR-T Europe to perform microbiological testing and review data in a cGMP QC lab. The role focuses on data integrity and patient safety while supporting investigations, CAPAs, audits and cross-functional collaboration.

Based in Beerse, the position is part of the weekend team, working Saturday and Sunday 6:00 AM to 6:00 PM, with emphasis on compliant documentation and continuous process improvement.

Qualifications

• Bachelor's degree in a scientific discipline or related field is required.
• Minimum of 2 years of experience in a cGMP-quality control lab or similar regulated environment.
• Knowledge of compendial requirements (USP, EP, JP) preferred.
• Experience with microbiological testing principles and data interpretation.
• Proficiency in Microsoft Office (Outlook, Excel, Word, PowerPoint).
• Excellent written and verbal communication; CAR-T/cell therapy or biopharmaceutical experience is desirable.

Responsabilités

• Perform microbiological testing and analytical activities per GMP and quality specifications.
• Review laboratory data for accuracy, completeness and data integrity.
• Author, revise, and maintain SOPs and lab documents in the management system.
• Support investigations, deviations, CAPAs, and quality activities.
• Assist with internal audits and maintain inspection readiness in QC Microbiology.
• Participate in cross-functional meetings and provide technical input.

Connaissances

Microbiological testing

Aseptic techniques

Endotoxin testing

Sterility testing

Environmental monitoring

MS Office

Communication skills

CAR-T/cell therapy experience

Formation

Bachelor's degree in a Scientific discipline

Outils

Document management system

Description du poste

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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:

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.

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.

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 and benefits for this position is:

Belgiium - form 54570 EUR- up to 73830EUR.