{"schemaVersion":"jobsearcher.job.v1","id":"2c3b629b559a37bd71144a98","url":"https://jobsearcher.com/jobs/2c3b629b559a37bd71144a98","canonicalUrl":"https://jobsearcher.com/jobs/2c3b629b559a37bd71144a98","title":"Validation Engineer","description":"Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500+ employees globally, with over 30+ locations in the US and global operations in 32 countries. We believe in providing staffing solutions to address the current talent gap – Right Talent – Right Time – Right Place – Right Price and acting as a Career Coach to our consultants.Company: One of Our ClientsJob Description:Job Title: Validation EngineerLocation: Devens, MA 01434Duration: 06+ Months (Extendable)Pay Rate: $48.00 - 51.04/hr on W2Must Haves:Bachelor's degree requiredIncumbents must have demonstrated experience in solving complex technical issues and have the skills and understanding to troubleshoot process defectsDemonstrated success in cross functional influencing, strong communication, and collaboration skillsMust have GMP experienceResponsibilities will include (but not limited to):Manage the entire lifecycle of QC laboratory instruments from procurement to qualification to decommissioning, ensuring all activities are in compliance with applicable policies/regulations.Design, execute, manage, and implement QC instrument/software qualification documents such as (but not limited to): User Requirement Specification (URS), Design Qualification (DQ), validation plans, equipment IOQ protocols, software test scripts, configuration specifications, risk assessments, qualification summary reportsAuthor/execute computer system validation scripts using an electronic validation database (ALM), or paper-basedOwn change controls specific to the qualification of QC instruments and its associated softwareUpdate the asset management database to reflect new assets, calibrations, preventative maintenancesAuthor instrument operational SOPs as neededCoordinate/interface/host vendors on siteChampions qualification deviations/software defects, identifying root causes and Corrective Actions/Preventive Actions (CA/PAs)Acts as the liaison between Digital Plant (IT) and lab departmentsExecute periodic assessments/decommissioning, as neededQualifications and Experience Required:Required Bachelor’s degree or Master’s degree in Engineering, Chemistry, Biology, or in a related, scientific/computer-based field.Minimum of 2 – 4+ years’ experience in the biopharmaceutical industry or equivalent combination of education and validation/lab experience will be considered.Quality management system experience including: document control/management, change controls, investigations, deviations, electronic validation databases, asset management databaseKnowledge of cGMP regulatory requirements, computerized analytical systems, i.e., 21 CFR part 11, GAMP, electronic record/electronic signature, data integrity, disaster recoveryIncumbents must have demonstrated experience in solving complex technical issues and have the skills and understanding to troubleshoot process defectsDemonstrated success in cross functional influencing, strong communication, and collaboration skillsMust have GMP experienceMicrosoft Office Applications, preferred.Computer system validation experience, preferredEquipment validation experience is a plusAwards and Accolades:America's Most Honored Businesses (Top 10%)Awarded by USPAAC for the Fastest Growing Business in the US12th Fastest Growing Staffing Company in USA by Staffing industry Analysts in the US (2020, 2019, 2020)Fastest 50 by NJ Biz (2020, 2019, 2020)INC 5000 Fastest growing for 8 consecutive years in a row (only 1.26% companies make it to this list)Top 100 by Dallas Business Journal (2020 and 2019)Proven Supplier of the Year by Workforce Logiq (2020 and 2019)2019 Spirit of Alliance Award by Agile12018 Best of the Best Platinum Award by Agile12018 TechServe Alliance Excellence Awards Winner2017 Best of the Best Gold Award by Agile1(Act1 Group)","company":"Net2Source","rawCompany":"net2source n2s","city":"Ayer","state":"MA","isRemote":false,"isActive":false,"createdAt":"2026-06-26T12:01:06.984Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"}],"industries":[{"code":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"},{"code":"541330","title":"Engineering Services","slug":"engineering-services"},{"code":"541380","title":"Testing Laboratories and Services","slug":"testing-laboratories-and-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Validation Engineer","description":"Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500+ employees globally, with over 30+ locations in the US and global operations in 32 countries. We believe in providing staffing solutions to address the current talent gap – Right Talent – Right Time – Right Place – Right Price and acting as a Career Coach to our consultants.Company: One of Our ClientsJob Description:Job Title: Validation EngineerLocation: Devens, MA 01434Duration: 06+ Months (Extendable)Pay Rate: $48.00 - 51.04/hr on W2Must Haves:Bachelor's degree requiredIncumbents must have demonstrated experience in solving complex technical issues and have the skills and understanding to troubleshoot process defectsDemonstrated success in cross functional influencing, strong communication, and collaboration skillsMust have GMP experienceResponsibilities will include (but not limited to):Manage the entire lifecycle of QC laboratory instruments from procurement to qualification to decommissioning, ensuring all activities are in compliance with applicable policies/regulations.Design, execute, manage, and implement QC instrument/software qualification documents such as (but not limited to): User Requirement Specification (URS), Design Qualification (DQ), validation plans, equipment IOQ protocols, software test scripts, configuration specifications, risk assessments, qualification summary reportsAuthor/execute computer system validation scripts using an electronic validation database (ALM), or paper-basedOwn change controls specific to the qualification of QC instruments and its associated softwareUpdate the asset management database to reflect new assets, calibrations, preventative maintenancesAuthor instrument operational SOPs as neededCoordinate/interface/host vendors on siteChampions qualification deviations/software defects, identifying root causes and Corrective Actions/Preventive Actions (CA/PAs)Acts as the liaison between Digital Plant (IT) and lab departmentsExecute periodic assessments/decommissioning, as neededQualifications and Experience Required:Required Bachelor’s degree or Master’s degree in Engineering, Chemistry, Biology, or in a related, scientific/computer-based field.Minimum of 2 – 4+ years’ experience in the biopharmaceutical industry or equivalent combination of education and validation/lab experience will be considered.Quality management system experience including: document control/management, change controls, investigations, deviations, electronic validation databases, asset management databaseKnowledge of cGMP regulatory requirements, computerized analytical systems, i.e., 21 CFR part 11, GAMP, electronic record/electronic signature, data integrity, disaster recoveryIncumbents must have demonstrated experience in solving complex technical issues and have the skills and understanding to troubleshoot process defectsDemonstrated success in cross functional influencing, strong communication, and collaboration skillsMust have GMP experienceMicrosoft Office Applications, preferred.Computer system validation experience, preferredEquipment validation experience is a plusAwards and Accolades:America's Most Honored Businesses (Top 10%)Awarded by USPAAC for the Fastest Growing Business in the US12th Fastest Growing Staffing Company in USA by Staffing industry Analysts in the US (2020, 2019, 2020)Fastest 50 by NJ Biz (2020, 2019, 2020)INC 5000 Fastest growing for 8 consecutive years in a row (only 1.26% companies make it to this list)Top 100 by Dallas Business Journal (2020 and 2019)Proven Supplier of the Year by Workforce Logiq (2020 and 2019)2019 Spirit of Alliance Award by Agile12018 Best of the Best Platinum Award by Agile12018 TechServe Alliance Excellence Awards Winner2017 Best of the Best Gold Award by Agile1(Act1 Group)","datePosted":"2026-06-26T12:01:06.984Z","dateModified":"2026-06-26T12:01:06.984Z","hiringOrganization":{"@type":"Organization","name":"Net2Source","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Ayer","addressRegion":"MA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"2c3b629b559a37bd71144a98"},"url":"https://jobsearcher.com/jobs/2c3b629b559a37bd71144a98"}}