{"schemaVersion":"jobsearcher.job.v1","id":"cf90fb2d5306a1fec615a96f","url":"https://jobsearcher.com/jobs/cf90fb2d5306a1fec615a96f","canonicalUrl":"https://jobsearcher.com/jobs/cf90fb2d5306a1fec615a96f","title":"Equipment Validation Engineer","description":"About the JobTitle: Validation SpecialistLocation: Framingham, MA (Onsite)Employment Type: Contract (6+ Months)Status: Accepting CandidatesAbout the RoleWe are seeking an experienced Validation Specialist to support qualification and validation activities in a GMP-regulated pharmaceutical/biotechnology manufacturing environment. This role will focus on equipment and utility validation, cleaning validation, temperature mapping, commissioning, and lifecycle support while ensuring compliance with cGMP, GDP, and regulatory requirements.Key ResponsibilitiesExecute cleaning validation protocols, sampling activities, and documentation.Perform temperature mapping, requalification, and monitoring of controlled temperature units (CTUs).Execute IQ/OQ/PQ protocols, equipment requalification, and periodic reviews for GMP equipment and utilities.Support commissioning, installation, qualification, and startup of new or modified manufacturing equipment.Collaborate with Engineering, Manufacturing, and Operations to troubleshoot equipment and validation issues.Author and review validation protocols, reports, SOPs, and supporting documentation.Support validation lifecycle activities, including change controls, deviations, investigations, and CAPAs.Maintain compliance with cGMP, GDP, FDA, and internal quality standards.Participate in audit readiness activities and support regulatory inspections.Work cross-functionally with Quality, Engineering, Manufacturing, and Validation teams.QualificationsBachelor's degree in Engineering, Life Sciences, or a related technical discipline.5+ years of hands-on validation experience in a GMP-regulated pharmaceutical or biotechnology environment.Experience with cleaning validation, equipment qualification (IQ/OQ/PQ), requalification, and validation lifecycle activities.Experience performing temperature mapping and controlled temperature unit (CTU) qualification.Strong understanding of cGMP, GDP, SOPs, change control, deviations, investigations, and CAPA processes.Excellent technical writing, documentation, and communication skills.Ability to manage multiple validation activities in a fast-paced manufacturing environment.Preferred QualificationsExperience supporting biologics, cell & gene therapy, or sterile manufacturing operations.Experience with commissioning and qualification (CQV) of GMP equipment and utilities.Familiarity with regulatory inspections (FDA, EMA) and audit support.Experience with validation management systems such as TrackWise, Veeva, Kneat, or similar.CompensationEstimated hourly range: $65–$75/hr (W-2).Final rate will be determined based on skills, experience, and interview outcome.","company":"JMD Technologies","rawCompany":"jmd technologies","city":"Framingham","state":"MA","isRemote":false,"isActive":false,"createdAt":"2026-07-01T10:38:23.099Z","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":"334510","title":"Electromedical and Electrotherapeutic Apparatus Manufacturing","slug":"electromedical-and-electrotherapeutic-apparatus-manufacturing"},{"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":"Equipment Validation Engineer","description":"About the JobTitle: Validation SpecialistLocation: Framingham, MA (Onsite)Employment Type: Contract (6+ Months)Status: Accepting CandidatesAbout the RoleWe are seeking an experienced Validation Specialist to support qualification and validation activities in a GMP-regulated pharmaceutical/biotechnology manufacturing environment. This role will focus on equipment and utility validation, cleaning validation, temperature mapping, commissioning, and lifecycle support while ensuring compliance with cGMP, GDP, and regulatory requirements.Key ResponsibilitiesExecute cleaning validation protocols, sampling activities, and documentation.Perform temperature mapping, requalification, and monitoring of controlled temperature units (CTUs).Execute IQ/OQ/PQ protocols, equipment requalification, and periodic reviews for GMP equipment and utilities.Support commissioning, installation, qualification, and startup of new or modified manufacturing equipment.Collaborate with Engineering, Manufacturing, and Operations to troubleshoot equipment and validation issues.Author and review validation protocols, reports, SOPs, and supporting documentation.Support validation lifecycle activities, including change controls, deviations, investigations, and CAPAs.Maintain compliance with cGMP, GDP, FDA, and internal quality standards.Participate in audit readiness activities and support regulatory inspections.Work cross-functionally with Quality, Engineering, Manufacturing, and Validation teams.QualificationsBachelor's degree in Engineering, Life Sciences, or a related technical discipline.5+ years of hands-on validation experience in a GMP-regulated pharmaceutical or biotechnology environment.Experience with cleaning validation, equipment qualification (IQ/OQ/PQ), requalification, and validation lifecycle activities.Experience performing temperature mapping and controlled temperature unit (CTU) qualification.Strong understanding of cGMP, GDP, SOPs, change control, deviations, investigations, and CAPA processes.Excellent technical writing, documentation, and communication skills.Ability to manage multiple validation activities in a fast-paced manufacturing environment.Preferred QualificationsExperience supporting biologics, cell & gene therapy, or sterile manufacturing operations.Experience with commissioning and qualification (CQV) of GMP equipment and utilities.Familiarity with regulatory inspections (FDA, EMA) and audit support.Experience with validation management systems such as TrackWise, Veeva, Kneat, or similar.CompensationEstimated hourly range: $65–$75/hr (W-2).Final rate will be determined based on skills, experience, and interview outcome.","datePosted":"2026-07-01T10:38:23.099Z","dateModified":"2026-07-01T10:38:23.099Z","hiringOrganization":{"@type":"Organization","name":"JMD Technologies","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Framingham","addressRegion":"MA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"cf90fb2d5306a1fec615a96f"},"url":"https://jobsearcher.com/jobs/cf90fb2d5306a1fec615a96f"}}