Quality Engineer

Piper Companies; Raleigh (NC); On-site; USD 228,682,000 - 272,765,000; Full time

Benefits offered by this job

Medical

Dental

Vision

401K

Job summary

Piper Companies seeks a Quality Engineer to join a leading pharmaceutical manufacturing organization in Raleigh, NC for a 3–6 month contract. The Quality Engineer will lead investigations, partner with plant personnel, and drive timely resolution of quality events in a GMP-regulated environment.

Responsibilities include leading deviations investigations, CAPA root-cause analysis, collaborating with production, engineering, and quality teams, reviewing quality documentation, and supporting

Qualifications

• 3+ years in a quality engineering/quality assurance/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.
• Ability to collaborate across functional teams and communicate technical findings to stakeholders.
• Bachelor's degree in Engineering, Chemistry, Biology, or related discipline preferred.

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 investigations align with GMP requirements and internal procedures.
• Assist with remediation tied to regulatory observations, audit findings, and quality system improvements.

Skills

Quality engineering

CAPA processes

GMP regulations

Cross-functional collaboration

Education

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

Job description

Piper Companies is seeking a Quality Engineer to join a leading pharmaceutical manufacturing organization for a three to six month contract opportunity located in Raleigh, NC. The Quality Engineer 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.

Responsibilities of the Quality Engineer include:

• Lead and support investigations related to deviations, non-conformances, and quality events occurring within the manufacturing environment.
• Partner closely with production, engineering, and quality teams to identify root causes and develop effective corrective and preventive actions (CAPAs).
• Perform shop floor assessments and gather technical information needed to resolve complex quality issues.
• Review quality documentation and ensure investigation activities are completed in accordance with GMP requirements and internal procedures.
• Assist with remediation efforts tied to regulatory observations, audit findings, and quality system improvement initiatives.

Qualifications for the Quality Engineer include:

• 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.
• Ability to collaborate effectively with cross-functional teams and communicate technical findings to stakeholders.
• Bachelor's degree in Engineering, Chemistry, Biology, or a related scientific discipline preferred.

Compensation for the Quality Engineer:

• Pay Rate: $80-$95 an hour
• Comprehensive Benefits: Medical, Dental, Vision, sick leave if required by law, and 401K

This job opens for applications on 8/23/26. Applications for this job will be accepted for at least 30 days from the posting date.

Keywords: quality engineer, GMP, pharmaceutical manufacturing, quality assurance, quality systems, CAPA, corrective action, preventive action, deviation investigations, root cause analysis, FDA regulations, audit readiness, compliance, manufacturing support, process improvement, quality events, non-conformance, validation, engineering, production support, remediation, regulatory inspections, documentation review, quality management, continuous improvement, chemical manufacturing, biologics, plant operations, investigation management, quality compliance.

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