GMP Quality Investigator—Root Cause & CAPA Expert

Accentuate Staffing; Raleigh (NC); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading staffing agency is seeking a Quality Investigator for a pharmaceutical manufacturing company in Raleigh, NC. This contract role involves conducting investigations related to site deviations and performing root cause analysis in a GMP environment. Ideal candidates will have 3–5+ years of experience in FDA-regulated settings, strong documentation skills, and knowledge of cGMPs. The position offers competitive pay and opportunities for continuous improvement initiatives within the organization.

Qualifications

• 3–5+ years of experience in a pharmaceutical, biotech, or FDA-regulated GMP environment.
• Hands-on experience conducting deviation and OOS investigations.
• Strong understanding of cGMPs, FDA regulations, and quality systems.

Responsibilities

• Conduct investigations related to site exceptions and deviations.
• Perform Phase II OOS investigations and support root cause analysis.
• Identify root causes and develop appropriate corrective actions.

Skills

Investigation experience

Root cause analysis

Collaboration across departments

Documentation practices

Education

Bachelor’s degree in Chemistry, Microbiology, Biology, Engineering, or related science

Tools

SAP

Microsoft Office

Job description

A leading staffing agency is seeking a Quality Investigator for a pharmaceutical manufacturing company in Raleigh, NC. This contract role involves conducting investigations related to site deviations and performing root cause analysis in a GMP environment. Ideal candidates will have 3–5+ years of experience in FDA-regulated settings, strong documentation skills, and knowledge of cGMPs. The position offers competitive pay and opportunities for continuous improvement initiatives within the organization.