Pharma Quality Engineer – GMP Investigator, 3–6 Mo

Piper Companies; Raleigh (NC); On-site; USD 110,000 - 131,000; Full time

Job summary

Piper Companies seeks a Quality Engineer for a three to six month contract in Raleigh, NC. The role will support site quality and manufacturing operations by leading investigations, partnering with plant personnel, and helping drive timely resolution of quality events in a GMP-regulated environment.

The position requires 3+ years in a similar role, hands-on investigations in pharma or related fields, and strong CAPA/GMP knowledge.

Qualifications

• 3+ years of experience in a quality engineering, quality assurance, or manufacturing support role within a regulated environment.
• Hands-on experience conducting investigations within a pharmaceutical, biologics, chemical, or related manufacturing facility.
• Strong understanding of GMP regulations, deviation management, root cause analysis, and CAPA processes.

Responsibilities

• Lead and support investigations related to deviations, non-conformances, and quality events in the manufacturing environment.
• Partner with production, engineering, and quality teams to identify root causes and develop CAPAs.
• Perform shop floor assessments and gather technical information to resolve quality issues.
• Review quality documentation and ensure investigation activities align with GMP requirements and internal procedures.
• Assist with remediation tied to regulatory observations, audit findings, and quality system improvement initiatives.

Skills

Investigations

CAPA

Root cause analysis

GMP compliance

Communication

Cross-functional collaboration

Education

Bachelor's degree in Engineering, Chemistry, Biology, or related

Job description

Piper Companies seeks a Quality Engineer for a three to six month contract in Raleigh, NC. The role will support site quality and manufacturing operations by leading investigations, partnering with plant personnel, and helping drive timely resolution of quality events in a GMP-regulated environment.

The position requires 3+ years in a similar role, hands-on investigations in pharma or related fields, and strong CAPA/GMP knowledge.