{"schemaVersion":"jobsearcher.job.v1","id":"af44a52a11a64f69c02452e5","url":"https://jobsearcher.com/jobs/af44a52a11a64f69c02452e5","canonicalUrl":"https://jobsearcher.com/jobs/af44a52a11a64f69c02452e5","title":"Process Engineer","description":"Summary DPS is looking for a CQV Engineer to work for a client in New Bedford, MA\n\nKey Responsibilities\n\nBecome familiar with the user, functional, installation, operation and performance requirements for assigned projects and tasks.\n\nReview requirements and source documentation P&IDs, RDs, URSs, SOPs, Specifications for use in development of equipment commissioning and validation documents.\n\nEquipment validation protocol development, including drafting documents, managing review cycles and protocol approval.\n\nSupport Validation Master Plan development.\n\nExecution of equipment validation protocols (including use of Kaye Validator/temperature monitoring for autoclaves, SIP Systems, washer COP, CIP, FITs, etc.).\n\nSupport Equipment Validation Report development, including drafting documents, managing review cycles and protocol approval.\n\nSupport Validation Summary Report development.\n\nPreparation and processing of turnover packaging and validation documentation in EDMQ (electronic document management system).\n\nProvide support for generation, resolution and closure of Equipment Validation related deviations and required documentation.\n\nAssist with coordination of activities between Client teams (validation, engineering, manufacturing, QC, etc.).\n\nSupport resolution of engineering/validation issues found during equipment validation.\n\nAttending meetings as required to support equipment installation and operation.\n\nProviding quality oversight and approval for validation documents as needed (Function test, IQs, OQs, etc.).\n\nSupport developing SOP’s.\n\nOther tasks as requested or required by Client to support Equipment Validation for each project.\n\nSkills & Qualifications\n\n3-5 Years of Equipment Validation experience working within a cGMP & FDA Regulated environment.\n\nPrevious experience with CQV activities for equipment outlined above.\n\nSupporting engineer will be resident at the Client facility or a previously agreed upon location (i.e. vendor’s location).\n\nA strong understanding and knowledge of equipment and automated systems is desired.\n\nSupport to be performed as required by the project schedules.\n\nPrevious Experience working in a cGMP and FDA regulated environment.\n\nCompany\nDPS Group is a global EPCM firm offering full-service solutions within the Life Sciences (pharmaceutical, biotechnology, and medical technology) and Advanced Technology (semiconductor, data center, and solar) industries. DPS is dedicated to delivering successful projects with a ‘client-first’ mentality and personal touch across a range of market sectors: Project and Program Management, Procurement, Design, Construction Management, Health and Safety Management, Commissioning, Qualification, and Start-up.\n\nEqual Opportunity Employer\nDPS Engineering Inc. is an Equal Opportunity Employer and employment selection decisions are based on merit, qualifications, and abilities. DPS does not discriminate in employment opportunities or practices on the basis of: race, color, religion, gender, national origin, age, sexual orientation, gender identity, disability, veteran status or any other characteristic protected by country, regional or local law.\n\n#J-18808-Ljbffr","company":"Arcadis","rawCompany":"arcadis","city":"Framingham","state":"MA","isRemote":false,"isActive":false,"createdAt":"2026-07-16T03:14:55.348Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"17-2199.00","title":"Engineers, All Other","slug":"engineers-all-other"},{"code":"17-3029.00","title":"Engineering Technologists and Technicians, Except Drafters, All Other","slug":"engineering-technologists-and-technicians-except-drafters-all-other"}],"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":"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":"Process Engineer","description":"Summary DPS is looking for a CQV Engineer to work for a client in New Bedford, MA\n\nKey Responsibilities\n\nBecome familiar with the user, functional, installation, operation and performance requirements for assigned projects and tasks.\n\nReview requirements and source documentation P&IDs, RDs, URSs, SOPs, Specifications for use in development of equipment commissioning and validation documents.\n\nEquipment validation protocol development, including drafting documents, managing review cycles and protocol approval.\n\nSupport Validation Master Plan development.\n\nExecution of equipment validation protocols (including use of Kaye Validator/temperature monitoring for autoclaves, SIP Systems, washer COP, CIP, FITs, etc.).\n\nSupport Equipment Validation Report development, including drafting documents, managing review cycles and protocol approval.\n\nSupport Validation Summary Report development.\n\nPreparation and processing of turnover packaging and validation documentation in EDMQ (electronic document management system).\n\nProvide support for generation, resolution and closure of Equipment Validation related deviations and required documentation.\n\nAssist with coordination of activities between Client teams (validation, engineering, manufacturing, QC, etc.).\n\nSupport resolution of engineering/validation issues found during equipment validation.\n\nAttending meetings as required to support equipment installation and operation.\n\nProviding quality oversight and approval for validation documents as needed (Function test, IQs, OQs, etc.).\n\nSupport developing SOP’s.\n\nOther tasks as requested or required by Client to support Equipment Validation for each project.\n\nSkills & Qualifications\n\n3-5 Years of Equipment Validation experience working within a cGMP & FDA Regulated environment.\n\nPrevious experience with CQV activities for equipment outlined above.\n\nSupporting engineer will be resident at the Client facility or a previously agreed upon location (i.e. vendor’s location).\n\nA strong understanding and knowledge of equipment and automated systems is desired.\n\nSupport to be performed as required by the project schedules.\n\nPrevious Experience working in a cGMP and FDA regulated environment.\n\nCompany\nDPS Group is a global EPCM firm offering full-service solutions within the Life Sciences (pharmaceutical, biotechnology, and medical technology) and Advanced Technology (semiconductor, data center, and solar) industries. DPS is dedicated to delivering successful projects with a ‘client-first’ mentality and personal touch across a range of market sectors: Project and Program Management, Procurement, Design, Construction Management, Health and Safety Management, Commissioning, Qualification, and Start-up.\n\nEqual Opportunity Employer\nDPS Engineering Inc. is an Equal Opportunity Employer and employment selection decisions are based on merit, qualifications, and abilities. DPS does not discriminate in employment opportunities or practices on the basis of: race, color, religion, gender, national origin, age, sexual orientation, gender identity, disability, veteran status or any other characteristic protected by country, regional or local law.\n\n#J-18808-Ljbffr","datePosted":"2026-07-16T03:14:55.348Z","dateModified":"2026-07-16T03:14:55.348Z","hiringOrganization":{"@type":"Organization","name":"Arcadis","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Framingham","addressRegion":"MA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"af44a52a11a64f69c02452e5"},"url":"https://jobsearcher.com/jobs/af44a52a11a64f69c02452e5"}}