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Associate Scientist Stability (Quality)

Job

Planet Pharma Group

Cleveland, OH (In Person)

Full-Time

Posted 3 weeks ago (Updated 2 weeks ago) • Actively hiring

Expires 7/6/2026

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Job Description

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