Associate Stability Scientist
Job Summary
Supporting the stability program operations, the full-time Associate Stability Scientist will manage stability study inventory, assist with data review, and ensure compliance with cGMP requirements while working onsite in New Brunswick, NJ.
Key responsibilities
- Manage stability study inventory, including sample receipt, storage, and testing coordination
- Assist in the execution of stability program activities for current and new products, including protocol generation and SOP documentation
- Provide administrative support for department training, financial processes, and recordkeeping
Required qualifications
- Bachelor's Degree in Chemistry, Microbiology, or a related scientific discipline
- Experience with stability programs and a solid understanding of cGMPs and regulatory principles
- Proficiency in computer software applications relevant to stability study management
- Ability to write and revise technical documents and SOPs
- Experience in maintaining accurate records and managing sample logistics
Complete Job Description
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