Quality Assurance Specialist Job at Catalent – Life Sciences Role in Greenville, NC
Are you passionate about ensuring quality and compliance in the pharmaceutical industry? Catalent, a global leader in contract development and manufacturing (CDMO), is looking for a Quality Assurance Specialist to join its team in Greenville, North Carolina. This role is ideal for professionals with a background in life sciences and quality assurance, offering a dynamic work environment, competitive benefits, and the opportunity to contribute to life-enhancing treatments.
About Catalent
Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) dedicated to developing, manufacturing, and supplying products that help people live better and healthier lives. With a focus on excellence in quality and compliance, Catalent supports pharma, biotech, and consumer health customers in product development, launch, and full life-cycle supply. Powered by experienced scientists, technicians, and cutting-edge technology, Catalent delivers billions of doses of life-enhancing treatments annually.
Job Description:
Job Posting: Quality Assurance Specialist
Location: Greenville, North Carolina, United States of America, 27834
Job Id: 0088409
Position Summary
The Quality Assurance Specialist at Catalent’s Greenville facility plays a key role in ensuring the integrity of data, maintaining quality standards, and fostering a culture of quality and safety across the organization. The Specialist will support various processes and projects while adhering to all relevant regulatory requirements.
The Role
- Ensure accurate transactions, documentation, and tracking of cGMP activities
- Advocate for quality standards and contribute to the development of a quality culture
- Foster open communication and information-sharing within teams
- Monitor and uphold quality and safety standards
- Review quality documentation and support analytical investigation teams
- Perform root cause analysis as needed
- Other duties as assigned
The Candidate
The ideal candidate will have a Bachelor’s or Associate’s degree in a life sciences discipline, along with professional experience in the pharmaceutical industry and quality assurance roles. Strong analytical skills, attention to detail, and the ability to handle objects using hands and arms are required.
Why You Should Join Catalent
- Competitive medical benefits and 401K
- 152 hours of PTO + 8 Paid Holidays
- Dynamic, fast-paced work environment
- Opportunity to work on Continuous Improvement Processes
Keywords: Catalent, Quality Assurance Specialist, Greenville, North Carolina, Pharmaceutical Industry, Quality Role
