QS Document Management Associate 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:
Non-Standard

Job Sub Function:
Workday Associate B

Job Category:
Non-Standard

All Job Posting Locations:
Gent, East Flanders, 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 

 

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.

 

 

We are searching for the best talent for a Quality Systems Document Management Associate CAR-T.

The position will be based in Ghent

 

The QS Document Management Associate CAR-T is responsible for quality systems document management support of the production of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP cleanroom environment.

Administrative Support within the Document & Training Management team.

 

 

You will be responsible for:

 


* You will be responsible for providing administrative support in both document management and training management, with a focus on compliant and efficient processes.


* Management of procedures and related documents in Truvault


* Management of training setup in Summit


* Fulfill the site key user responsibilities: represent CAR-T Belgium in global forums and team meetings, mentor site users for the document management process, and control access to the system


* Maintain a clear archive in line with Worldwide Record Information Management policies


* Perform tasks in accordance with Janssen/Johnson & Johnson policies, quality systems, and cGMP requirements


* Attend regularly scheduled team meetings and training


* May participate in process improvement and training


* May be assigned as a coach or mentor to less experienced colleagues

 

 

Experience and Skills


* A bachelor degree is required


* Experience with document management systems (Truvault) and training ...