Analist Biotech - Antwerpen, België - Johnson & Johnson

Johnson & Johnson

Geverifieerd bedrijf

Antwerpen, België

3 weken geleden

Geplaatst door:

Sophie Dubois

beBee Recruiter

Beschrijving

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 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
Provide input and take actions as a QC representative at crosslaboratory meetings

Qualifications:

Qualifications - External

A minimum of a bachelor's degree 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.
Excellent written and oral communication skill are required