ProPharma is seeking a Quality Record Investigation Lead Consultant to support a client in reviewing, investigating, documenting, and closing low-risk non-conformance and batch-related records within a six-week timeframe. This role requires the consultant to work on-site at the client's facility in Chicago, IL. The ideal candidate will possess strong investigation, documentation, and batch record review/closure experience, and be comfortable working independently within the client environment. The consultant will be responsible for overall execution, milestone management, and delivery performance.
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Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed