{"schemaVersion":"jobsearcher.job.v1","id":"b63d388317985b6a7741ef5e","url":"https://jobsearcher.com/jobs/b63d388317985b6a7741ef5e","canonicalUrl":"https://jobsearcher.com/jobs/b63d388317985b6a7741ef5e","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 Title: Contractor, CSV/CQV SpecialistLocation: Bend, OR 97703 (Onsite)Duration: 09 Month Contract (Extendable)Pay Rate range: $90.00 – 97.00/hr on W2 Hiring Manager NotesImmediate need due to a significant CQV validation backlog.Strong preference for candidates with analytical laboratory experience.Must be comfortable balancing priorities between CQV and Instrumentation teams.Onsite presence in Bend is required to support instrument qualification and field execution activities.Candidates with both CSV and CQV experience will be highly preferred. Key Responsibilities Develop, execute, review, and maintain validation lifecycle documentation, including:Risk AssessmentsUser Requirement Specifications (URS)Design SpecificationsTraceability MatricesTest ScriptsValidation ProtocolsDiscrepancies and DeviationsSummary ReportsPeriodic Review DocumentationSystem Retirement DocumentationSupport qualification and validation activities for new and existing analytical laboratory instruments, computerized systems, and GMP equipment.Execute and support Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) activities.Ensure calibration readiness, data integrity verification, and compliance with 21 CFR Part 11 and Annex 11 requirements.Partner with Quality Control, Instrumentation, Engineering, Automation, Quality Assurance, and system owners to plan and execute validation activities.Prepare and support change controls, impact assessments, deviations, CAPAs, and validation protocols related to GMP equipment, analytical instruments, and computerized systems.Utilize and support the Kneat validation platform, including document creation, workflow routing, approvals, and record closure.Assist with Kneat template development and continuous improvement initiatives.Maintain inspection-ready documentation in accordance with SOPs, GxP requirements, and site procedures.Monitor field execution activities, identify gaps early, drive discrepancy resolution, and escalate issues as appropriate.Split support between the Instrumentation team for CSV activities and the CQV group for qualification execution, documentation updates, and readiness activities.Travel between Bend campus buildings as needed to support laboratory instrument and equipment qualification activities.Perform other duties as assigned. Education: Bachelor's Degree in Engineering, Life Sciences, Chemistry, Biology, or a related scientific discipline preferred. ExperienceMinimum 3-5 years of CQV and/or CSV experience within pharmaceutical, biotechnology, or other regulated industries.Experience supporting analytical laboratory instruments and equipment qualification.Experience working in cGMP-regulated environments.Experience with computerized systems validation and equipment qualification.Experience managing multiple validation projects and competing priorities.Previous backlog remediation or high-volume validation support experience is highly desirable. Technical KnowledgeProven experience using Kneat validation/documentation software.Strong understanding of GMP documentation requirements and validation practices.Knowledge of:GxP regulations21 CFR Part 1121 CFR Parts 210 and 211EU Annex 11Annex 15USP and ASTM standardsUnderstanding of computerized systems, laboratory instruments, pharmaceutical manufacturing equipment, specifications, procedures, and engineering drawings.Strong understanding of equipment qualification versus instrument validation requirements. Key CompetenciesExcellent technical writing and documentation skills.Strong organization and attention to detail.Ability to prioritize effectively across multiple projects and stakeholders.Proactive problem-solving skills.Ability to work both independently and collaboratively in a regulated environment.Strong communication and cross-functional collaboration skills.Commitment to quality, compliance, and data integrity. Physical & Environmental RequirementsWork within a clean, secure, and regulated GMP environment.Wear required PPE, including lab coats, safety glasses, gloves, and other protective equipment as required.Occasional lifting of up to 50 pounds.Travel between site buildings as needed.Flexible schedule to support project activities.Regards,Prateek PampattiwarRecruitment SpecialistNet2Source Inc.Global HQ Address –270 Davidson Ave, Suite 704, Somerset, NJ 08873, USAOffice: (201) 340-8700 x 324 | Cell: (551) 220 3007| Fax: (201) 221-8131| Email: Pampattiwar.Prateek@net2source.com","company":"Net2Source","rawCompany":"net2source n2s","city":"South Bend","state":"IN","isRemote":false,"isActive":false,"createdAt":"2026-08-23T07:22:24.738Z","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":"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 Title: Contractor, CSV/CQV SpecialistLocation: Bend, OR 97703 (Onsite)Duration: 09 Month Contract (Extendable)Pay Rate range: $90.00 – 97.00/hr on W2 Hiring Manager NotesImmediate need due to a significant CQV validation backlog.Strong preference for candidates with analytical laboratory experience.Must be comfortable balancing priorities between CQV and Instrumentation teams.Onsite presence in Bend is required to support instrument qualification and field execution activities.Candidates with both CSV and CQV experience will be highly preferred. Key Responsibilities Develop, execute, review, and maintain validation lifecycle documentation, including:Risk AssessmentsUser Requirement Specifications (URS)Design SpecificationsTraceability MatricesTest ScriptsValidation ProtocolsDiscrepancies and DeviationsSummary ReportsPeriodic Review DocumentationSystem Retirement DocumentationSupport qualification and validation activities for new and existing analytical laboratory instruments, computerized systems, and GMP equipment.Execute and support Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) activities.Ensure calibration readiness, data integrity verification, and compliance with 21 CFR Part 11 and Annex 11 requirements.Partner with Quality Control, Instrumentation, Engineering, Automation, Quality Assurance, and system owners to plan and execute validation activities.Prepare and support change controls, impact assessments, deviations, CAPAs, and validation protocols related to GMP equipment, analytical instruments, and computerized systems.Utilize and support the Kneat validation platform, including document creation, workflow routing, approvals, and record closure.Assist with Kneat template development and continuous improvement initiatives.Maintain inspection-ready documentation in accordance with SOPs, GxP requirements, and site procedures.Monitor field execution activities, identify gaps early, drive discrepancy resolution, and escalate issues as appropriate.Split support between the Instrumentation team for CSV activities and the CQV group for qualification execution, documentation updates, and readiness activities.Travel between Bend campus buildings as needed to support laboratory instrument and equipment qualification activities.Perform other duties as assigned. Education: Bachelor's Degree in Engineering, Life Sciences, Chemistry, Biology, or a related scientific discipline preferred. ExperienceMinimum 3-5 years of CQV and/or CSV experience within pharmaceutical, biotechnology, or other regulated industries.Experience supporting analytical laboratory instruments and equipment qualification.Experience working in cGMP-regulated environments.Experience with computerized systems validation and equipment qualification.Experience managing multiple validation projects and competing priorities.Previous backlog remediation or high-volume validation support experience is highly desirable. Technical KnowledgeProven experience using Kneat validation/documentation software.Strong understanding of GMP documentation requirements and validation practices.Knowledge of:GxP regulations21 CFR Part 1121 CFR Parts 210 and 211EU Annex 11Annex 15USP and ASTM standardsUnderstanding of computerized systems, laboratory instruments, pharmaceutical manufacturing equipment, specifications, procedures, and engineering drawings.Strong understanding of equipment qualification versus instrument validation requirements. Key CompetenciesExcellent technical writing and documentation skills.Strong organization and attention to detail.Ability to prioritize effectively across multiple projects and stakeholders.Proactive problem-solving skills.Ability to work both independently and collaboratively in a regulated environment.Strong communication and cross-functional collaboration skills.Commitment to quality, compliance, and data integrity. Physical & Environmental RequirementsWork within a clean, secure, and regulated GMP environment.Wear required PPE, including lab coats, safety glasses, gloves, and other protective equipment as required.Occasional lifting of up to 50 pounds.Travel between site buildings as needed.Flexible schedule to support project activities.Regards,Prateek PampattiwarRecruitment SpecialistNet2Source Inc.Global HQ Address –270 Davidson Ave, Suite 704, Somerset, NJ 08873, USAOffice: (201) 340-8700 x 324 | Cell: (551) 220 3007| Fax: (201) 221-8131| Email: Pampattiwar.Prateek@net2source.com","datePosted":"2026-08-23T07:22:24.738Z","dateModified":"2026-08-23T07:22:24.738Z","hiringOrganization":{"@type":"Organization","name":"Net2Source","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"South Bend","addressRegion":"IN","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"b63d388317985b6a7741ef5e"},"url":"https://jobsearcher.com/jobs/b63d388317985b6a7741ef5e"}}