QC Analyst Biotech

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 .

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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 Janssen Supply Chain Group, a member of the Johnson & Johnson family of companies, is recruiting QC analysts for the CAR-T hub in Europe.

The position will be based in Beerse Belgium.

CAR-T (chimeric antigen receptor T-cell therapy) is an innovative approach to eliminate cancer cells, which work by harnessing the power of a patient's own immune system.

They are created from the patients' own T cells and are engineered to eliminate cancer cells expressing a specific antigen.

To support the CAR-T program in EMEA, Janssen is building two CAR-T manufacturing centers in the Ghent area (Belgium).

The QC laboratories will be operated from the existing Janssen Beerse site.

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

Major 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 SOPs, 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
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