Specialist I, Quality Assurance
Catalent
- Location
- Kansas City, MO
- Work style
- On-site
- Job type
- Full time
- Posted
- Nov 2
- 2 days ago
Career path
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About the company
Catalent
Pharmaceuticals · 10,001+ employees
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. 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. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
What you'll do
- Support clinical trial projects ensuring compliance with regulatory requirements
- Implement and maintain quality assurance processes throughout the product lifecycle
- Ensure documentation is accurate, up-to-date and properly maintained
- Create Certificate of Analysis with supervision
- Participate in continuous improvement initiatives related to quality management
What you need
- 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
- 20/30 corrected vision exam with colorblindness testing
- Nurse assessment and pulmonary physical
- Respirator fit test
- DEA background check relating to controlled substance products
- Ability to work in refrigerator and/or freezer environments and near machinery
- Ability to identify aberrant data and potential quality or compliance concerns and escalate to management (preferred)
Key skills
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Perks
- Paid time off
- 8 paid holidays
- Medical
- Dental
- Vision
- Tuition reimbursement
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