Quality Specialist I
Catalent Pharma SolutionsKansas City, Missouri, United States
Posted March 27, 2026
Full Time
About the Company
Catalent is a leading global contract development and manufacturing organization (CDMO) dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers.
Job Description
The Quality 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). They are responsible for implementing and maintaining quality assurance processes throughout the product lifecycle.
Requirements
- Participate in continuous improvement initiatives to enhance process, systems, and procedures related to quality management
- Review QC data for completeness and acceptability
- Approve Release packets with supervision
- Lead Investigator for Deviations and Complaints
- Hosting CAPA review and deviation management meetings
- Reviewing /approve change controls and change actions with supervision
Benefits
- Competitive medical benefits
- 401K
- 152 hours PTO
- 8 Paid Holidays