Principal Scientist, Cell Therapy Method Development

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:
Discovery & Pre-Clinical/Clinical Development

Job Sub Function:
Biotherapeutics R&D

Job Category:
Scientific/Technology

All Job Posting Locations:
Malvern, Pennsylvania, United States of America

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 a Principal Scientist, Cell Therapy Method Development to be onsite in Malvern, PA. 
 

Purpose:
The Biotherapeutics Development - Analytical Development (BioTD - AD) group is seeking an upbeat, highly motivated Principal Scientist to focus on potency analytical development for cell therapy modality.

The individual would work with the team to develop functional potency strategies for lentivirus and CAR-T cells that will be endorsed by the health authorities.

A successful candidate will have experience with the design, execution and optimization of a broad range of cell-based assays and will have the opportunity to engage in multi-functional teams.

They will learn from and contribute to industry-leading drug discovery/development programs that has brought numerous quality therapeutics to patients and has made significant contributions to human health.

You will be responsible for:
•    Leading method development, validation, tech transfer, and lifecycle support activities for cell-based potency methods.
•    Work collaboratively on a matrix environment, supporting and mentoring team members.
•    Supporting regulatory filings, including INDs and BLAs.
•    Representing the department on cross-functional and external teams and act as a technical expert on potency.
•    Communicating complex technical concepts to partners.
•    Accurately capturing data in a timely manner, including maintenance of detailed records in compliance with applicable cGMP, safety, and environmental requirements.

Qualifications / Requirements:
 

Education:
•    A minimum of a Bachelor's degree is required
•    Advanced degree (Master's, PhD) is preferred
 

Required:
•    Minimum ...