This role is 100% on-site at the Holly Springs, NC facility, working a standard weekday schedule (8am 5pm) with some flexibility (start between 7 9am).

The ideal candidate will bring at least 3 year of industry experience within a GMP-regulated biotech or pharmaceutical environment. They must demonstrate strong knowledge of quality systems and QC laboratory operations with a proven ability to write, own, and drive closure of quality records, including deviations, CAPAs, and change controls.
This role requires excellent written communication, grammar, and investigative leadership skills. Candidates should be detail-oriented, proactive, and able to navigate shifting priorities in a fast-paced environment with minimal oversight. They will collaborate with multiple cross-functional teams and should be confident leading meetings and pushing investigations independently through to completion.

Experience with Veeva Quality Systems is highly desirable.

This posit...