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

The QC analyst, CAR-T Europe is responsible for preparing and conducting test 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.

This role is based on a weekend shift: Saturdays and Sundays, from 6:00 to 18:00 h.

Your responsibilities:

• 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 SOP’s, WIs and Protocols to support daily operations of the lab using the document management system

• Support laboratory related investigation records and CAPAs Assist in the execution of internal audits

• Provide input to functional laboratory meetings

• Provide input and take 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

• Ensuring order and tidiness

• Reporting (near) accidents, incidents, deviations and risky situations

• Contributing to and proposing solutions to improve safety, health and the environment

• Actively taking part in promotional campaigns

• Addressing other employees and third parties when prevention procedures are not followed or when unsafe behavior is reported

Requirements & Qualifications

• A minimum of a bachelor’s 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/or Potency assays is required

• Basic knowledge 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.

• Excellent written and oral communication skills are required

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

Required Skills: Preferred Skills: