Stability Coordinator
Catalent Pharma SolutionsSaint Petersburg, Florida, United States
Posted March 16, 2026
Full Time
About the Company
Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
Job Description
The Stability Coordinator will support the site's Stability Program by generating stability protocols, initiating stability studies, and ensuring compliance with cGMP, SOPs, and ICH guidelines.
Requirements
- Bachelor's degree in a related scientific discipline
- 3 years of experience with documentation systems and cGMP-compliant environments
- Experience with LIMS and sample tracking preferred
- Strong organizational, technical writing, and communication skills
- Knowledge of stability program expectations, sample handling, data integrity, and QMS principles
- Proficiency with Microsoft Outlook, Excel, and Word
Benefits
- 152 hours of PTO + 8 paid holidays
- Day-one benefits
- Career growth in a state-of-the-art, turn-key facility
