{"schemaVersion":"jobsearcher.job.v1","id":"01a94d95e60296dc34eced57","url":"https://jobsearcher.com/jobs/01a94d95e60296dc34eced57","canonicalUrl":"https://jobsearcher.com/jobs/01a94d95e60296dc34eced57","title":"CQV Engineer (Commissioning, Qualification & Validation)","description":"CQV Engineer (Commissioning, Qualification & Validation)\nLocation: Indianapolis, IN\nTravel: Up to 40% domestic & international travel\n\nBring Critical Manufacturing Systems to Life\n\nWe bring advanced manufacturing to life by delivering world‑class automation, validation, and instrumentation solutions. Our teams solve complex challenges, support industry‑leading facilities, and make a measurable impact on critical manufacturing operations every day.\n\nWe are looking for a CQV Engineer to join our Indianapolis, IN team. In this position, you will support the commissioning, qualification, and validation of manufacturing systems, equipment, facilities, utilities, and automation systems within regulated pharmaceutical environments. You will work on high‑impact capital projects that help transform complex systems into operational, compliant, and production‑ready assets.\n\nResponsibilities\n\nDevelop and drive completion of Commissioning & Qualification (C&Q) deliverables, including validation plans, risk assessments, project strategies, user requirements, functional specifications, design specifications, impact assessments, traceability matrices, test cases, engineering studies, and final summary reports.\n\nApply a strong understanding of commissioning and qualification principles to support project execution and regulatory compliance activities.\n\nSupport pharmaceutical capital projects for:\n\nActive pharmaceutical ingredient (API) manufacturing equipment\n\nFilling operations\n\nDevice assembly systems\n\nPackaging equipment\n\nFacilities and utilities\n\nAutomation systems\n\nParticipate in project review meetings, including design reviews, qualification reviews, testing strategy discussions, execution reviews, and project status meetings.\n\nDevelop, review, and maintain validation and qualification documentation within electronic lifecycle management systems.\n\nAssess, document, and support change management activities resulting from design updates, deviations, and testing outcomes.\n\nParticipate in Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT) activities.\n\nComplete required client training and site‑specific onboarding requirements.\n\nPerform other duties as assigned.\n\nQualifications\n\nBachelor's degree in Biomedical or Chemical Engineering.\n\nExperience with Commissioning & Qualification (C&Q) deliverables, CQV activities, validation documentation, or relevant academic/project experience.\n\nStrong understanding of validation principles and deliverables, including requirements development, design, testing, and reporting.\n\nStrong interpersonal, verbal, written, and presentation communication skills.\n\nHighly motivated, results‑driven mindset with the ability to manage multiple priorities in a fast‑paced environment.\n\nDemonstrated project management skills and the ability to independently drive assignments to completion.\n\nAbility to travel up to 40% domestically and internationally.\n\nWhy Join PACIV\n\nWork on pharmaceutical manufacturing and life sciences capital projects.\n\nGain hands‑on experience with commissioning, qualification, validation, FAT, and SAT activities.\n\nCollaborate with experienced engineering, automation, and validation professionals.\n\nBuild expertise working with manufacturing systems, utilities, facilities, and automation technologies.\n\nContribute to projects that support critical manufacturing operations and production readiness.\n\nCompensation & Benefits\n\nGenerous Paid Time Off: Vacation, Sick Leave, and Company Holidays\n\nPACIV pays 90% of yearly health care premiums\n\nHealth Savings Account (HSA) with Company Contributions\n\n401(k) with Company Match up to 4% and immediate vesting with enrollment\n\nEqual Opportunity Employer\n\nPACIV is an Equal Opportunity Employer and considers all qualified applicants in accordance with applicable federal, state, and local employment laws. Employment is contingent upon successful completion of applicable pre‑employment requirements and verification of authorization to work in the United States.\n\n#J-18808-Ljbffr","company":"Process Automation Controlsinstrumentsvalidations","rawCompany":"process automation controlsinstrumentsvalidations","city":"Indianapolis","state":"IN","isRemote":false,"isActive":false,"createdAt":"2026-07-05T03:32:26.940Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"},{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"541330","title":"Engineering Services","slug":"engineering-services"},{"code":"334513","title":"Instruments and Related Products Manufacturing for Measuring, Displaying, and Controlling Industrial Process Variables","slug":"instruments-and-related-products-manufacturing-for-measuring-displaying-and-controlling-industrial-process-variables"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"CQV Engineer (Commissioning, Qualification & Validation)","description":"CQV Engineer (Commissioning, Qualification & Validation)\nLocation: Indianapolis, IN\nTravel: Up to 40% domestic & international travel\n\nBring Critical Manufacturing Systems to Life\n\nWe bring advanced manufacturing to life by delivering world‑class automation, validation, and instrumentation solutions. Our teams solve complex challenges, support industry‑leading facilities, and make a measurable impact on critical manufacturing operations every day.\n\nWe are looking for a CQV Engineer to join our Indianapolis, IN team. In this position, you will support the commissioning, qualification, and validation of manufacturing systems, equipment, facilities, utilities, and automation systems within regulated pharmaceutical environments. You will work on high‑impact capital projects that help transform complex systems into operational, compliant, and production‑ready assets.\n\nResponsibilities\n\nDevelop and drive completion of Commissioning & Qualification (C&Q) deliverables, including validation plans, risk assessments, project strategies, user requirements, functional specifications, design specifications, impact assessments, traceability matrices, test cases, engineering studies, and final summary reports.\n\nApply a strong understanding of commissioning and qualification principles to support project execution and regulatory compliance activities.\n\nSupport pharmaceutical capital projects for:\n\nActive pharmaceutical ingredient (API) manufacturing equipment\n\nFilling operations\n\nDevice assembly systems\n\nPackaging equipment\n\nFacilities and utilities\n\nAutomation systems\n\nParticipate in project review meetings, including design reviews, qualification reviews, testing strategy discussions, execution reviews, and project status meetings.\n\nDevelop, review, and maintain validation and qualification documentation within electronic lifecycle management systems.\n\nAssess, document, and support change management activities resulting from design updates, deviations, and testing outcomes.\n\nParticipate in Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT) activities.\n\nComplete required client training and site‑specific onboarding requirements.\n\nPerform other duties as assigned.\n\nQualifications\n\nBachelor's degree in Biomedical or Chemical Engineering.\n\nExperience with Commissioning & Qualification (C&Q) deliverables, CQV activities, validation documentation, or relevant academic/project experience.\n\nStrong understanding of validation principles and deliverables, including requirements development, design, testing, and reporting.\n\nStrong interpersonal, verbal, written, and presentation communication skills.\n\nHighly motivated, results‑driven mindset with the ability to manage multiple priorities in a fast‑paced environment.\n\nDemonstrated project management skills and the ability to independently drive assignments to completion.\n\nAbility to travel up to 40% domestically and internationally.\n\nWhy Join PACIV\n\nWork on pharmaceutical manufacturing and life sciences capital projects.\n\nGain hands‑on experience with commissioning, qualification, validation, FAT, and SAT activities.\n\nCollaborate with experienced engineering, automation, and validation professionals.\n\nBuild expertise working with manufacturing systems, utilities, facilities, and automation technologies.\n\nContribute to projects that support critical manufacturing operations and production readiness.\n\nCompensation & Benefits\n\nGenerous Paid Time Off: Vacation, Sick Leave, and Company Holidays\n\nPACIV pays 90% of yearly health care premiums\n\nHealth Savings Account (HSA) with Company Contributions\n\n401(k) with Company Match up to 4% and immediate vesting with enrollment\n\nEqual Opportunity Employer\n\nPACIV is an Equal Opportunity Employer and considers all qualified applicants in accordance with applicable federal, state, and local employment laws. Employment is contingent upon successful completion of applicable pre‑employment requirements and verification of authorization to work in the United States.\n\n#J-18808-Ljbffr","datePosted":"2026-07-05T03:32:26.940Z","dateModified":"2026-07-05T03:32:26.940Z","hiringOrganization":{"@type":"Organization","name":"Process Automation Controlsinstrumentsvalidations","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Indianapolis","addressRegion":"IN","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"01a94d95e60296dc34eced57"},"url":"https://jobsearcher.com/jobs/01a94d95e60296dc34eced57"}}