MFG Operator Cryopreservation CAR T

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

Job Function:
Supply Chain Manufacturing

Job Sub Function:
Manufacturing Assembly

Job Category:
Business Enablement/Support

All Job Posting Locations:
Raritan, New Jersey, United States of America

Job Description:

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

We are searching for the best talent for MFG Operator Cryopreservation CAR T to be in Raritan, NJ.

Purpose:

This position is responsible for performing manufacturing procedures and the execution of scheduled tasks within a CGMP environment.

This position is responsible for quality and maintaining the highest standards in compliance within company policies, procedures, and all applicable regulations.

Responsible for fostering site pride and J&J citizenship. 

You will be responsible for:



* Be part of the manufacturing operations team responsible for production of autologous CAR-T products for clinical and commercial operation in a controlled current Good Manufacturing Practice (cGMP) cleanroom environment. 


* Independently execute manufacturing or manufacturing-support processes according to standard operating procedures and current curriculum.  


* Execute manufacturing activities common to cell culturing, purification, aseptic processing, and cryopreservation using appropriate techniques. 


* Perform process unit operations according to standard operating procedures and batch records, and record production data and information in a clear, concise, format according to Good Documentation Practices (GDP). 


* Perform tasks on time in a manner consistent with quality systems and cGMP requirements. 


* Work in a team based, cross-functional environment to complete production tasks required by shift schedule. 


* Aid in the development of manufacturing processes including appropriate documentation. 


* Drive continuous improvement of manufacturing operations leveraging own observation as well as input of team members. 


* Handle human derived materials in containment areas. 


* Support schedule adj...