{"schemaVersion":"jobsearcher.job.v1","id":"db6a05eaf02a7a5e01f1b6bb","url":"https://jobsearcher.com/jobs/db6a05eaf02a7a5e01f1b6bb","canonicalUrl":"https://jobsearcher.com/jobs/db6a05eaf02a7a5e01f1b6bb","title":"Process Engineer","description":"BiologicsLocation: Wilson, NCTravel: Limited domestic/international travel as requiredRole OverviewWe are seeking an experienced Process Engineer to support a large-scale Large Molecule Drug Substance (LMDS) manufacturing project in Wilson, NC. This role drives the engineering design, start-up, commissioning, qualification (C&Q), and operational readiness for a GMP biologics facility. You will partner cross-functionally with Technical Operations, Quality, Validation, Automation, and external A&E/construction partners to deliver safe, compliant, and efficient manufacturing solutions.Key ResponsibilitiesC&Q Execution: Lead process systems through installation, start-up, commissioning, and qualification. System Ownership: Serve as the Subject Matter Expert (SME) for GMP large molecule manufacturing equipment. CAPEX Support: Drive strategic capital projects from design through execution and operational handover. Tech Transfer: Provide technical leadership for technology transfers and process-fit-to-plant activities. Troubleshooting: Provide hands-on troubleshooting and design modifications to support evolving plant needs. Compliance: Ensure all activities strictly align with GMP, safety, regulatory, and quality standards. Required QualificationsEducation: Bachelor s degree in Chemical, Mechanical, or Biochemical Engineering (or related discipline). Experience: 8+ years of process/plant engineering experience in GMP large molecule biologics facilities. Facility Start-ups: Proven experience supporting greenfield or brownfield GMP facility start-ups (process systems, utilities, automation). Project Management: Track record of managing complex CAPEX projects and process improvements simultaneously. Work Authorization: Must be legally authorized to work in the US (open to US-based travelers and relocation). Presence: Ability to work onsite full-time in Wilson, NC. Preferred QualificationsSpecialized expertise in drug substance tech transfers or process-fit-to-plant activities. Advanced degree (MS, MBA, PhD), PE license, or FPX certification. Experience with Six Sigma, Lean methodologies, and managing A&E/construction partners.","company":"Qvalfocus","rawCompany":"qvalfocus","city":"Wilson","state":"NC","isRemote":false,"isActive":false,"createdAt":"2026-11-04T09:35:33.854Z","occupations":[{"code":"17-2041.00","title":"Chemical Engineers","slug":"chemical-engineers"},{"code":"17-2199.00","title":"Engineers, All Other","slug":"engineers-all-other"},{"code":"17-2112.03","title":"Manufacturing Engineers","slug":"manufacturing-engineers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"},{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Process Engineer","description":"BiologicsLocation: Wilson, NCTravel: Limited domestic/international travel as requiredRole OverviewWe are seeking an experienced Process Engineer to support a large-scale Large Molecule Drug Substance (LMDS) manufacturing project in Wilson, NC. This role drives the engineering design, start-up, commissioning, qualification (C&Q), and operational readiness for a GMP biologics facility. You will partner cross-functionally with Technical Operations, Quality, Validation, Automation, and external A&E/construction partners to deliver safe, compliant, and efficient manufacturing solutions.Key ResponsibilitiesC&Q Execution: Lead process systems through installation, start-up, commissioning, and qualification. System Ownership: Serve as the Subject Matter Expert (SME) for GMP large molecule manufacturing equipment. CAPEX Support: Drive strategic capital projects from design through execution and operational handover. Tech Transfer: Provide technical leadership for technology transfers and process-fit-to-plant activities. Troubleshooting: Provide hands-on troubleshooting and design modifications to support evolving plant needs. Compliance: Ensure all activities strictly align with GMP, safety, regulatory, and quality standards. Required QualificationsEducation: Bachelor s degree in Chemical, Mechanical, or Biochemical Engineering (or related discipline). Experience: 8+ years of process/plant engineering experience in GMP large molecule biologics facilities. Facility Start-ups: Proven experience supporting greenfield or brownfield GMP facility start-ups (process systems, utilities, automation). Project Management: Track record of managing complex CAPEX projects and process improvements simultaneously. Work Authorization: Must be legally authorized to work in the US (open to US-based travelers and relocation). Presence: Ability to work onsite full-time in Wilson, NC. Preferred QualificationsSpecialized expertise in drug substance tech transfers or process-fit-to-plant activities. Advanced degree (MS, MBA, PhD), PE license, or FPX certification. Experience with Six Sigma, Lean methodologies, and managing A&E/construction partners.","datePosted":"2026-11-04T09:35:33.854Z","dateModified":"2026-11-04T09:35:33.854Z","hiringOrganization":{"@type":"Organization","name":"Qvalfocus","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Wilson","addressRegion":"NC","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"db6a05eaf02a7a5e01f1b6bb"},"url":"https://jobsearcher.com/jobs/db6a05eaf02a7a5e01f1b6bb"}}