Quality Control Analyst, Car-T Critical Reagents (1 Of 4)

Janssen Pharmaceuticals, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for a Quality Control Analyst, CAR-T Critical Reagents (1 of 4)! This position will be located in Raritan, NJ.

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 https://www.jnj.com/.

Janssen Biotech, Inc., one of the Janssen Pharmaceutical Companies of Johnson & Johnson, and Legend Biotech USA Inc., have entered into a global, strategic collaboration to develop, manufacture, and commercialize a chimeric antigen receptor (CAR) T-cell therapy. This innovative strategic partnership is designed to combine the strengths and expertise of two companies to advance the promise of an immunotherapy CAR T platform and investigational treatment.

Are you interested in joining a team that is positively impacting patients' lives by ensuring high quality in our cell therapy products? Apply today for this exciting opportunity to be part of the #CAR-T team!

The Quality Control (QC) Analyst is responsible for preparing and conducting testing of critical reagents used by the QC laboratories. They are responsible for ensuring testing is completed in adherence with all applicable procedures, standards, and GMP regulations.

Key Responsibilities:

• Conduct analytical testing to qualify critical reagents used in the CAR-T QC laboratories

• Perform analytical testing in compliance with all applicable procedures, GMP, and GDP regulations

• Ensure a safe work environment by following guidelines in environmental, health, and safety regulations

• Perform peer review of laboratory data

• Collaborate and coordinate with testing laboratories to acquire the data necessary to prepare documentation and issue Certificate of Analysis

• Author and update SOPs, WIs, and Protocols 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-functional meetings