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Unicon Pharma Inc · Frederick, Maryland
Hiring: QC Compliance & Data Review Specialist III (Contract)
Frederick, MD (Onsite)
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? DM me your updated resume!
Details
| Company | Unicon Pharma Inc |
| Location | Frederick, Maryland |
| Type | FULL TIME |
| Niche | Full-time |