HTP Excipient Method Development Co-op

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:
Career Programs

Job Sub Function:
Non-LDP Intern/Co-Op

Job Category:
Career Program

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

Johnson & Johnson Innovative Medicine, a division of Johnson & Johnson’s Family of Companies is recruiting for a 2025 Co-OP to implement automated analytics for excipient/impurity analysis.

This position will be located in Malvern, PA.

Within Johnson & Johnson Innovative Medicine, Therapeutics Development & Supply (TDS) organization is responsible for the development, clinical supply, marketed product support, and life cycle management of Biotherapeutics.

Within TDS, the Analytical Development, Process Analytical Science (AD-PAS) group supports routine sample testing, method development, and validation, for product development and characterization.

The AD-PAS team is recruiting for a Co-OP to collaborate in migrating analytical assays from manual processes to fully automated end to end workflows.

In this role,  you will collaborate with Assay Development SMEs, and end-users to increase sample testing throughput and/or reduce hands-on time, time-to-result, and assay variability.

The primary scientific area of focus will be excipient/impurity assays, implementing automated analytical workflows such as TECAN automated liquid handler, and chromatography, programming/operating the TECAN and performing routine testing of manually/automation prepared samples.

Primary Responsibilities:

Depending on your skills and interest the responsibilities will include:


* Collaborate with cross-functional team to design, develop, and deploy TECAN script to prepare samples for excipient/impurity tests.


* Operate / troubleshoot the TECAN liquid handler to prepare samples for excipient/impurity tests.


* Manually prepare samples for excipient/impurity tests.


* Compare results between automated and manually prepared sample preparations.


* Optimize existing automated solutions to p...