On-Site Quality Records Investigator (6-Week Project)

ProPharma; Raleigh (NC); On-site; USD 70,000 - 90,000; 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 their facility in Chicago, IL. All work will be conducted on-site for this project, with independence to operate within the client environment.

The role emphasizes strong investigation, documentation, and batch record review/closure experience, milestone management, and delivery performance.

Qualifications

• Strong investigation, documentation, and batch record review/closure experience.
• Able to work independently within client environment.

Responsibilities

• Review assigned records
• Perform investigations and documentation activities
• Complete Record closure activities
• Escalate issues, exceptions, and support needs appropriately

Skills

Investigation

Documentation

Batch record review

Record closure

Independent worker

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 their facility in Chicago, IL. All work will be conducted on-site for this project, with independence to operate within the client environment.

The role emphasizes strong investigation, documentation, and batch record review/closure experience, milestone management, and delivery performance.