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