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/. Johnson & Johnson Innovative Medicine, a division of Johnson & Johnson's Family of Companies, is recruiting for a 2025 Spring Co-OP to implement automated analytics for excipient/impurity analysis. This position will be located in Malvern, PA. Johnson & Johnson Innovative Medicine is the pharmaceutical company of Johnson & Johnson, and you can count on us to keep working diligently to make that future a reality for patients everywhere, by fighting sickness with science, improving access with ingenuity, and healing hopelessness with heart. We focus on areas of medicine where we can make the biggest difference: Cardiovascular & Metabolism, Immunology, Infectious Diseases & Vaccines, Neuroscience, Oncology, and Pulmonary Arterial Hypertension. We never stop working toward a future where disease is a thing of the past. 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 efficiency 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/automated prepared samples. Key Responsibilities: \r 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 provide new functionality. Ensure data integrity through accurate and timely data capture/entry into appropriate electronic systems. \r \r