Quality Engineer - 173405

Responsibilities: Conduct thorough investigations of deviations, nonconformances, and quality events to determine root cause and product impact within GMP manufacturing operations. Partner directly with production personnel and plant leadership to gather data, evaluate processes, and assess manufacturing-related quality concerns. Lead and author corrective and preventive action (CAPA) activities, ensuring timely closure and alignment with regulatory expectations. Support ongoing remediation initiatives stemming from previous regulatory observations and quality system improvement efforts. Perform on-site assessments of manufacturing processes, equipment, and operational controls to strengthen compliance and inspection readiness. Qualifications: Bachelor's degree in Engineering, Chemistry, Quality Assurance, Manufacturing, Life Sciences, or a related technical field. 5+ years of experience supporting GMP-regulated manufacturing environments with a strong emphasis on investigations and CAPA management. Proven ability to perform hands-on root cause analysis within manufacturing facilities and effectively partner with operations teams. Working knowledge of FDA regulations, cGMP requirements, quality systems, and deviation management processes. Experience within chemical manufacturing, specialty chemicals, pharmaceutical manufacturing, or other process-driven production environments strongly preferred. Candidates whose backgrounds are primarily focused on biologics may be less aligned unless they possess significant traditional manufacturing experience. Compensation: Salary Range: $75/hr - $95/hr (flexibility available for highly qualified candidates with directly relevant experience) Comprehensive Benefits: Medical, Dental, Vision, sick leave if required by law, and 401K Application Details Location: Raleigh, NC Work Schedule: On-site, 5 days per week Employment Type: Contract (3-6 month engagement) Posting Date: 8/31/2026 Apply By / Closing Date: Open Until Filled