Hourly - GMP Quality Assurance Specialist

Budd Group•Holly Springs, NC

1d•$25•Onsite

About The Position

As our GMP Quality Assurance Specialist, you will be the bridge between technical compliance and frontline execution. You will act as a Quality Control Auditor and Compliance Lead to ensure every logbook and cleaning task meets stringent standards.

Requirements

3+ years GMP experience (Pharma/Biotech preferred)
Audit experience
Valid Driver’s License
At least 3 years in a GMP-regulated environment (Pharma, Biotech, or Medical Device).
An exceptional ability to spot errors in dense technical documentation and logbook entries.
Proficiency in Microsoft Office and facility management software; ability to draft clear SOPs and technical reports.
Ability to stand/walk for long periods and lift up to 50 lbs.

Nice To Haves

Bilingual (Spanish/English) is strongly preferred to effectively train our diverse frontline workforce.

Responsibilities

Conduct daily audits of GMP logbooks to ensure ALCOA+ documentation principles (Attributable, Legible, Contemporaneous, Original, Accurate) are followed.
Act as the site subject matter expert, identifying GDP errors and overseeing the correction process.
Perform site-wide technical inspections to ensure janitorial activities meet site SOPs and "cleanroom" standards.
Design and deliver high-impact training programs for frontline associates on chemical safety, equipment routines, and documentation.
Investigate root causes for any missed standards and implement Corrective and Preventive Actions (CAPA).