QA Auditor: Manufacturing; Onsite, Day-One
Listed on 2026-10-07
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Quality Assurance - QA/QC
Regulatory Compliance Specialist -
Pharmaceutical
Regulatory Compliance Specialist
Catalent Pharma Solutions in Greenville, NC is seeking a Quality Assurance Auditor - Manufacturing to perform routine and non-routine QA tasks supporting internal clients and commercial processes. The role is 100% onsite, Monday–Friday, 8:00am–5:00pm, with a focus on data integrity and GMP compliance.
If you bring a Bachelor’s or Associate degree with relevant pharma experience and a track record in batch records review and on-the-floor QA, you will help sustain a culture of quality and safety
Are you ready to take on the QA Auditor:
Manufacturing (Onsite, Day-One Benefits) role at Catalent Pharma Solutions?
Learn more about the QA Auditor:
Manufacturing (Onsite, Day-One Benefits) role in the description above.
We appreciate your interest in this position.
Join Catalent Pharma Solutions and contribute to our ongoing work.
Take a moment to read everything above and see whether this role is right for you.
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