Associate Scientist - Stability (Quality)

Position Summary We are seeking a detail‑oriented and motivated Associate Scientist to support analytical stability studies within a cGMP‑regulated environment. This role focuses on executing stability programs, managing samples, and ensuring data integrity and regulatory compliance. Key Responsibilities Perform stability testing using analytical techniques such as: HPLC GC Karl Fischer (KF) Other physicochemical methods Support stability study execution in compliance with ICH, FDA, and regulatory guidelines Coordinate sample management , including stability chambers and inventory tracking Generate, review, and maintain: Stability protocols Analytical data Study reports Conduct OOS (Out-of-Specification) investigations and support CAPA activities Ensure all laboratory work complies with cGMP standards Collaborate with cross‑functional teams and clients to support product quality initiatives Qualifications Education: Bachelor’s degree in Chemistry or related scientific field Experience: ~2+ years in an analytical or quality lab (cGMP environment preferred) Experience with HPLC and standard lab instrumentation Preferred: Stability or QC lab experience Familiarity with ICH stability guidelines Experience with OOS investigations Core Skills Strong analytical and problem-solving abilities Hands‑on lab skills (sample prep, assays, impurity testing) Ability to manage multiple priorities in a fast‑paced environment Strong communication and teamwork skills #J-18808-Ljbffr Planet Pharma Group