Lead Quality Investigation Consultant - Batch Records

ProPharma; Raleigh (NC); On-site; USD 90,000 - 130,000; 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 the client site in Chicago, IL. The role requires strong investigation, documentation, and batch record review experience and the ability to work independently in a client environment.

You will interface with the client, manage milestones, provide weekly status updates, escalate risks, and oversee team productivity while supporting

Qualifications

• Strong investigation, documentation and batch record review experience.
• On-site at Chicago, IL for six-week project.
• Ability to manage milestones, deliverables and client communications.

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

Skills

Project management

Investigation

Documentation

Batch records

Risk management

Client liaison

Education

Bachelor's degree in life sciences or related

Tools

TrackWise

Microsoft Excel

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 the client site in Chicago, IL. The role requires strong investigation, documentation, and batch record review experience and the ability to work independently in a client environment.

You will interface with the client, manage milestones, provide weekly status updates, escalate risks, and oversee team productivity while supporting