Hiring: QC Compliance & Data Review Specialist III (Contract)
Frederick, MD (Onsite)
Monday–Friday | 8:30 AM–5:00 PM
Please double check you have the right level of experience and qualifications by reading the full overview of this opportunity below.
We’re looking for an experienced QC Compliance & Data Review Specialist to support quality operations in a GMP-regulated pharmaceutical, biologics, or cell therapy environment.
Key Responsibilities & Requirements:
- Perform independent GMP laboratory data reviews and ensure data integrity in accordance with ALCOA+ principles.
- Manage quality records, including deviations, CAPAs, change controls, and laboratory investigations.
- Ensure compliance with cGMP, Good Documentation Practices, and FDA regulations.
- Support OOS/OOT investigations, audit readiness, and product release documentation.
- Experience with eQMS/LIMS platforms; Veeva, GVault, or TrackWise is preferred.
Interested? xzgxqkn DM me your updated resume!
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