Quality Assurance Auditor - Manufacturing
Catalent · Greenville, NC
QualityFull timeCompany career page
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Role summary
Quality Assurance Auditor role at a pharmaceutical oral solid dose manufacturing facility in Greenville, North Carolina. Responsible for ensuring cGMP compliance, data integrity, batch record review, and real-time quality support across manufacturing and packaging operations.
What they're looking for
- Bachelor's degree plus 3 years pharmaceutical industry experience with 1 year direct QA role
- Or Associate degree plus 4 years pharmaceutical experience with 2 years direct QA role
- Minimum 1 year batch record review and on-floor quality assurance manufacturing support
- Ability to handle and manipulate objects using hands and arms
- Knowledge of cGMP regulations and compendial requirements
- Experience with standard operating procedures and quality documentation
What you'll be doing
- Ensure data integrity and accurate documentation of all cGMP activities and transactions
- Perform in-process quality checks and assure material release prior to manufacturing operations
- Review batch records and provide real-time support to manufacturing and packaging teams
- Monitor compliance with internal, client-specific, and compendial requirements across operations
- Promote quality culture and continuous improvement through cross-functional communication and advocacy
Privacy & handoff
This role links to Catalent's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.