Lead Quality Records Investigator & Project Lead

PPG US ProPharma Group, LLC; Raleigh (NC); On-site; USD 55,000 - 96,000; Full time

Job summary

ProPharma 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.

Qualifications

• Experience in investigations and non-conformance closures.
• Experience reviewing batch-related records and documentation.
• Ability to work independently in a client environment.

Responsibilities

• Primary client interface and project oversight.
• Manage milestones, KPI tracking, and weekly reporting.
• Escalate risks and issues; oversee team productivity.
• Support exception and non-conformance investigations and closures.

Skills

Project management

KPI tracking

Weekly status reporting

Risk management

Team leadership

Investigation experience

Job description

ProPharma 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.