{"schemaVersion":"jobsearcher.job.v1","id":"d4cdaf3d342d3fb22409c2e6","url":"https://jobsearcher.com/jobs/d4cdaf3d342d3fb22409c2e6","canonicalUrl":"https://jobsearcher.com/jobs/d4cdaf3d342d3fb22409c2e6","title":"Process Engineer","description":"Job Title: Process Engineer\n\nLocation: Richmond, IL\n\nDuration: Long Term\n\nPosition Overview\nWe are seeking a Process Engineer to support process validation, risk management, and engineering activities within a regulated manufacturing environment. This role will focus on validation execution, design documentation, risk assessments, process improvements, and cross-functional project coordination while ensuring compliance with quality and regulatory requirements.\n\nKey Responsibilities\n\nLead and coordinate process validation activities, including IQ, OQ, and PQ execution.\n\nDevelop, review, and maintain engineering and validation documentation.\n\nAuthor and review risk management documents, including Process FMEA (pFMEA).\n\nSupport design transfer activities and process implementation projects.\n\nCoordinate with cross-functional teams on equipment installation and validation activities.\n\nPerform risk assessments and identify opportunities for process improvements.\n\nSupport statistical analysis, Design of Experiments (DOE), and Test Method Validation (TMV) activities.\n\nCollaborate with Quality, Manufacturing, and Engineering teams to ensure project success.\n\nEnsure compliance with design controls, quality systems, and regulatory requirements.\n\nRequired Qualifications\n\nBachelor's Degree in Engineering or a related technical discipline.\n\n2+ years of engineering experience within a regulated industry.\n\nHands‑on experience with Process Validation (IQ/OQ/PQ).\n\nExperience with Risk Management methodologies, including FMEA.\n\nKnowledge of ISO 13485 and quality system requirements.\n\nFamiliarity with design controls and engineering documentation.\n\nUnderstanding of statistical analysis, DOE, and validation principles is preferred.\n\nProficiency with Microsoft Office applications.\n\nStrong problem‑solving, communication, and project coordination skills.\n\n#J-18808-Ljbffr","company":"Stark Pharma Solutions","rawCompany":"stark pharma solutions","city":"Richmond","state":"IL","isRemote":false,"isActive":true,"createdAt":"2026-07-08T03:22:48.189Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"17-2199.00","title":"Engineers, All Other","slug":"engineers-all-other"},{"code":"17-2112.00","title":"Industrial Engineers","slug":"industrial-engineers"}],"industries":[{"code":"541330","title":"Engineering Services","slug":"engineering-services"},{"code":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"},{"code":"333248","title":"All Other Industrial Machinery Manufacturing","slug":"all-other-industrial-machinery-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Process Engineer","description":"Job Title: Process Engineer\n\nLocation: Richmond, IL\n\nDuration: Long Term\n\nPosition Overview\nWe are seeking a Process Engineer to support process validation, risk management, and engineering activities within a regulated manufacturing environment. This role will focus on validation execution, design documentation, risk assessments, process improvements, and cross-functional project coordination while ensuring compliance with quality and regulatory requirements.\n\nKey Responsibilities\n\nLead and coordinate process validation activities, including IQ, OQ, and PQ execution.\n\nDevelop, review, and maintain engineering and validation documentation.\n\nAuthor and review risk management documents, including Process FMEA (pFMEA).\n\nSupport design transfer activities and process implementation projects.\n\nCoordinate with cross-functional teams on equipment installation and validation activities.\n\nPerform risk assessments and identify opportunities for process improvements.\n\nSupport statistical analysis, Design of Experiments (DOE), and Test Method Validation (TMV) activities.\n\nCollaborate with Quality, Manufacturing, and Engineering teams to ensure project success.\n\nEnsure compliance with design controls, quality systems, and regulatory requirements.\n\nRequired Qualifications\n\nBachelor's Degree in Engineering or a related technical discipline.\n\n2+ years of engineering experience within a regulated industry.\n\nHands‑on experience with Process Validation (IQ/OQ/PQ).\n\nExperience with Risk Management methodologies, including FMEA.\n\nKnowledge of ISO 13485 and quality system requirements.\n\nFamiliarity with design controls and engineering documentation.\n\nUnderstanding of statistical analysis, DOE, and validation principles is preferred.\n\nProficiency with Microsoft Office applications.\n\nStrong problem‑solving, communication, and project coordination skills.\n\n#J-18808-Ljbffr","datePosted":"2026-07-08T03:22:48.189Z","dateModified":"2026-07-08T03:22:48.189Z","hiringOrganization":{"@type":"Organization","name":"Stark Pharma Solutions","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Richmond","addressRegion":"IL","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"d4cdaf3d342d3fb22409c2e6"},"url":"https://jobsearcher.com/jobs/d4cdaf3d342d3fb22409c2e6"}}