{"schemaVersion":"jobsearcher.job.v1","id":"467185215a7a64de163aa07e","url":"https://jobsearcher.com/jobs/467185215a7a64de163aa07e","canonicalUrl":"https://jobsearcher.com/jobs/467185215a7a64de163aa07e","title":"Equipment Validation Engineer","description":"Job Title: GMP Equipment Validation Engineer – CQV\r\nLocation: Oceanside, CA\r\nWe are seeking a highly motivated and detail-oriented GMP Equipment Validation Engineer to support Commissioning, Qualification, and Validation (CQV) activities for a range of manufacturing and utility equipment at a client site. This role is ideal for someone who thrives in a dynamic environment, can work independently, and is confident interfacing directly with client teams.\r\nOur CQV team collaborates closely with the client across multiple facets of controls and automation, ensuring seamless integration and compliance with regulatory standards. The ideal candidate will bring strong technical expertise, excellent communication skills, and a proactive approach to problem-solving. The ideal candidate has experience leading the equipment CQV efforts of a team that also includes computer system validation engineers and specialists.\r\nKey Responsibilities\r\nLead and execute CQV activities for GMP equipment including\r\nAutoclaves\r\nCIP/SIP systems\r\nBioreactors\r\nIncubators\r\nFreezers\r\nRefrigerators\r\nCentrifuges\r\nWashers\r\nControlled temperature units\r\nEnvironmental chambers\r\nHVAC systems\r\nClean steam generators\r\nWFI systems\r\nProcess tanks\r\nUtility systems (compressed air, nitrogen, etc.)\r\nDevelop and review validation documentation including URS, DQ, IQ, OQ, and PQ protocols and reports.\r\nPerform risk assessments and impact analyses to support validation strategy.\r\nCoordinate with client engineering, automation, and quality teams to ensure alignment on project goals and timelines.\r\nTroubleshoot and resolve equipment and process issues during commissioning and qualification phases.\r\nMaintain compliance with cGMP, FDA, and other applicable regulatory requirements.\r\nProvide timely updates and communicate effectively with client stakeholders.\r\nQualifications\r\nBachelor's degree in engineering, Life Sciences, or related field.\r\n3+ years of experience in CQV within a GMP-regulated environment.\r\nStrong understanding of validation lifecycle and regulatory expectations.\r\nExperience with automated systems and controls integration is a plus.\r\nExcellent organizational and communication skills.\r\nAbility to work independently and manage multiple priorities.\r\nBenefits\r\nPremium medical coverage\r\n401(k) with company match\r\nTuition reimbursement\r\nUnique performance incentives\r\nAnd more — all designed to support your growth, well-being, and future.\r\nValspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.\r\nJ-18808-Ljbffr","company":"SupportFinity","rawCompany":"supportfinity","city":"Oceanside","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-07-16T01:42:06.237Z","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":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Equipment Validation Engineer","description":"Job Title: GMP Equipment Validation Engineer – CQV\r\nLocation: Oceanside, CA\r\nWe are seeking a highly motivated and detail-oriented GMP Equipment Validation Engineer to support Commissioning, Qualification, and Validation (CQV) activities for a range of manufacturing and utility equipment at a client site. This role is ideal for someone who thrives in a dynamic environment, can work independently, and is confident interfacing directly with client teams.\r\nOur CQV team collaborates closely with the client across multiple facets of controls and automation, ensuring seamless integration and compliance with regulatory standards. The ideal candidate will bring strong technical expertise, excellent communication skills, and a proactive approach to problem-solving. The ideal candidate has experience leading the equipment CQV efforts of a team that also includes computer system validation engineers and specialists.\r\nKey Responsibilities\r\nLead and execute CQV activities for GMP equipment including\r\nAutoclaves\r\nCIP/SIP systems\r\nBioreactors\r\nIncubators\r\nFreezers\r\nRefrigerators\r\nCentrifuges\r\nWashers\r\nControlled temperature units\r\nEnvironmental chambers\r\nHVAC systems\r\nClean steam generators\r\nWFI systems\r\nProcess tanks\r\nUtility systems (compressed air, nitrogen, etc.)\r\nDevelop and review validation documentation including URS, DQ, IQ, OQ, and PQ protocols and reports.\r\nPerform risk assessments and impact analyses to support validation strategy.\r\nCoordinate with client engineering, automation, and quality teams to ensure alignment on project goals and timelines.\r\nTroubleshoot and resolve equipment and process issues during commissioning and qualification phases.\r\nMaintain compliance with cGMP, FDA, and other applicable regulatory requirements.\r\nProvide timely updates and communicate effectively with client stakeholders.\r\nQualifications\r\nBachelor's degree in engineering, Life Sciences, or related field.\r\n3+ years of experience in CQV within a GMP-regulated environment.\r\nStrong understanding of validation lifecycle and regulatory expectations.\r\nExperience with automated systems and controls integration is a plus.\r\nExcellent organizational and communication skills.\r\nAbility to work independently and manage multiple priorities.\r\nBenefits\r\nPremium medical coverage\r\n401(k) with company match\r\nTuition reimbursement\r\nUnique performance incentives\r\nAnd more — all designed to support your growth, well-being, and future.\r\nValspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.\r\nJ-18808-Ljbffr","datePosted":"2026-07-16T01:42:06.237Z","dateModified":"2026-07-16T01:42:06.237Z","hiringOrganization":{"@type":"Organization","name":"SupportFinity","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Oceanside","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"467185215a7a64de163aa07e"},"url":"https://jobsearcher.com/jobs/467185215a7a64de163aa07e"}}