Quality Specialist I
Catalent Pharma SolutionsKansas City, Missouri, United States
Posted May 12, 2026
Full Time
About the Company
Catalent is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives.
Job Description
Quality Assurance Specialist I supports clinical trial projects, ensuring all work is performed in compliance with regulatory requirements, good manufacturing practices (cGMP) and standard operating procedures (SOPs).
Requirements
- Bachelor's degree in a scientific discipline or equivalent knowledge and experience.
- High school degree with 2+ years of Quality Assurance experience in a GMP manufacturing environment.
- Ability to identify aberrant data and potential quality/compliance concerns escalating to management.
- Ability to work effectively under pressure to meet deadlines.
Benefits
- Competitive medical benefits
- 401K
- 152 hours PTO
- 8 Paid Holidays