Join a dynamic team as a Scientist in Stability, driving product stability strategies for large molecule drugs, and ensuring robust compliance with global manufacturing standards and regulatory requirements.

Optimize stability programs and strategies for large molecule drug substances and products. Oversee stability data analysis, lead cross-functional teams, and ensure compliance with regulatory requirements while driving business continuity.

Join a team that's enhancing laboratory workflows by maintaining and improving the Veeva LIMS system, collaborating with IT and lab staff to ensure compliance, data integrity, and user training for optimal laboratory operations.

Support stability program operations by managing studies, coordinating samples, and ensuring compliance with cGMP regulations. Engage in data review, documentation, and team training, contributing to the success of global biopharmaceutical stability efforts.

Lead the QA team in driving quality excellence within a cGMP Cell Therapy environment. Oversee day-shift operations, coaching managers and ensuring compliance while enhancing team capabilities and solving complex quality issues.