Associate II, Quality Assurance
Catalent Pharma SolutionsKansas City, Missouri, United States
Posted April 6, 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
The Kansas City Clinical and Specialty Services (CSS) Quality Associate II 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
- High School diploma or GED
- 1-3 years packaging experience or related industry experience, preferred
- Ability to follow a variety of instructions furnished in written, oral, diagram, or schedule form
- Mathematical and scientific reasoning ability
- Sufficient skills and knowledge in the use of computers and associated computer technology
Benefits
- 152 hours of PTO + 8 paid holidays
- Several Employee Resource Groups focusing on D&I
- Generous 401K match
- Medical, dental and vision benefits effective day one of employment
- Tuition Reimbursement
- WellHub- program to promote overall physical wellness
- Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories