Quality Record Investigation Lead Consultant

ProPharma•Raleigh, NC
•Onsite

About The Position

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.

Requirements

  • Strong investigation experience
  • Strong documentation experience
  • Strong batch record review/closure experience
  • Comfortable working independently within the client environment

Responsibilities

  • Primary client interface
  • Project management and KPI tracking
  • Weekly status reporting
  • Risk and issue escalation
  • Team oversight and productivity management
  • Support execution of exception and non-conformance investigations and closures as needed
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