QC CAR-T Investigation Coordinator (weekend)

Johnson & Johnson Co.; Geel; On-site; EUR 52,000 - 83,000; Full time

Benefits offered by this job

Annual bonus

Vacation days

Parental leave

Bereavement leave

Well-being reimbursement

Job summary

Johnson & Johnson Beerse, Belgium is seeking a QC CAR-T Investigation Coordinator to join the Innovative Medicine Supply Chain Group. The weekend team role runs Saturdays and Sundays from 6:00 AM to 6:00 PM, supporting daily QC operations and investigations in a GMP-regulated environment.

Responsibilities include leading investigations, implementing corrective actions, coordinating with multiple departments, and delivering QC training.

Qualifications

• Master’s degree in biochemistry, biotechnology, or a related field; or a Bachelor’s degree with relevant experience.
• Knowledge of cGMP regulations and FDA/EU guidance is required.
• Excellent written and verbal communication skills; ability to work independently in a GMP-regulated environment.

Responsibilities

• Support daily QC operations in collaboration with supervisors, analysts, Production, Warehouse, and QA.
• Lead QC investigations and prepare final investigation reports based on root cause analysis.
• Define and implement corrective actions and monitor their effectiveness.
• Coordinate cross-departmental QC investigations and serve as the QC representative.
• Develop and deliver training or awareness sessions within QC.

Skills

GMP experience

Microsoft Office

Strong communication

Education

Master’s degree in biochemistry, biotechnology, or related field

Bachelor’s degree with relevant experience

Job description

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: Quality Job Sub Function: Quality Assurance Job Category: Professional 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

CAR-T is an innovative treatment for blood cancer that harnesses the power of a patient’s own immune system. By genetically modifying the patient’s T-cells to recognize and eliminate cancer cells, this advanced technology offers new hope to patients for whom other therapies have provided limited or no benefit.

To support the expansion of CAR-T treatment capacity in Europe, we are looking for talented and motivated colleagues to join our CAR-T hub. The Innovative Medicine Supply Chain Group, a member of the Johnson & Johnson family of companies, is recruiting a QC CAR-T Investigation Coordinator based in Beerse, Belgium. This position is part of the weekend team, working Saturday and Sunday from 6:00 AM to 6:00 PM.

As part of the QC team, your key responsibilities will include:

• Supporting daily QC operations in close collaboration with supervisors, analysts, Production, Warehouse, and QA.
• Leading QC investigations and preparing final investigation reports based on thorough root cause analysis.
• You will define and implement corrective actions, monitor their effectiveness, and ensure timely execution and closure.
• For cross-departmental QC investigations, you will coordinate a multidisciplinary team and act as the QC representative.
• Developing and delivering training or awareness sessions within QC.

Qualifications

Master’s degree in biochemistry, biotechnology, or a related field; or a Bachelor’s degree with relevant experience. Knowledge of cGMP regulations and FDA/EU guidance is required. Strong organizational skills, with the ability to work independently, flexibly, and accurately. Excellent written and verbal communication skills. Professional experience in a GMP-regulated environment, preferably within Quality Control, is an advantage. Very good knowledge of Microsoft Office applications. Exposure to and practical experience with molecular and cell biology techniques, including PCR, Flow Cytometry, ELISA, Cell Culture, and Mycoplasma testing, would be highly beneficial and is considered a preferred qualification.

#RPOEMEA

Required Skills:

Preferred Skills:

The anticipated base pay range for this position is: €52.000,00 - €82.685,00

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.

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.