Senior Stability Associate

Role: Support stability studies and GMP scale-up activities within R&D operations, focusing on sample management, documentation, and compliance. Responsibilities include executing stability testing for GMP and experimental lots, maintaining inventory and labeling within LIMS and Record Management Systems, and performing chamber chart monitoring and training as needed. Requirements: 2-4 years of experience, understanding of analytical testing, GxP, SOPs, and health authority regulations; strong communication skills; ability to work autonomously and handle physical tasks. HighValue: molecular or biologic stability testing, GMP compliance, R&D support, documentation control. WorkSetup: Office/laboratory environment; no travel specified.