Lead Quality Records Investigator & Project Lead
Listed on 2026-10-17
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Business
Regulatory Compliance Specialist
Pro Pharma is seeking a consultant to review, investigate, document, and close low-risk non-conformance and batch-related records within a six-week timeframe at our Chicago, IL facility. All work will be conducted on-site for this project.
The consultant will serve as the primary client interface, oversee project milestones, KPI tracking, and weekly status reporting, and manage risk and issue escalation. They will provide team oversight to ensure timely execution and closures.
As a Lead Quality Records Investigator & Project Lead, you will play an important part at PPG US Pro Pharma Group, LLC in Raleigh, NC, United States.
All applications are reviewed carefully by our team.
The position is based in Raleigh, NC, United States.
This opportunity is part of our work in Management & Operations, Consulting.
The advertised compensation is 55.000 - 96.000.
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