{"schemaVersion":"jobsearcher.job.v1","id":"83acef2cbd8f6534174a1f82","url":"https://jobsearcher.com/jobs/83acef2cbd8f6534174a1f82","canonicalUrl":"https://jobsearcher.com/jobs/83acef2cbd8f6534174a1f82","title":"Validation Engineer (OPT/CPT)","description":"Are you a talented Validation Engineer seeking new opportunities in the US? Join Validation Associates LLC, a specialist pharmaceutical recruitment & staffing consultancy, focused on providing expert services in the life sciences industry.\nResponsibilities:\nPerform equipment qualification, process validation, and cleaning validation activities.\nDevelop and execute validation protocols, including IQ/OQ/PQ.\nConduct risk assessments, root cause analysis, and failure mode effects analysis (FMEA).\nCollaborate with cross-functional teams to ensure compliance with regulatory standards.\nMaintain accurate documentation and reports related to validation activities.\nStay updated on industry regulations and guidelines.\nRequirements:\nBachelors or Master's degree in Engineering, Life Sciences, or related field.\nPrevious experience in validation activities within the pharmaceutical or medical device industry.\nFamiliarity with regulatory guidelines, including FDA regulations and 21 CFR Part 11.\nStrong problem-solving and analytical skills.\nKnowledge of GMP, GDP, and quality systems.\nProficiency in validation software and tools.\nExcellent communication and teamwork abilities.\nBenefits:\nCompetitive compensation package.\nExciting opportunities in the life sciences industry.\nContinuous professional development and training programs.\nCollaborative and supportive work environment.\nCareer growth and advancement opportunities.\nJob Type: Contract\nPay: $30.00 - $33.00 per hour\nBenefits:\n401(k)\n401(k) matching\nDental insurance\nEmployee assistance program\nHealth insurance\nLife insurance\nPaid time off\nProfessional development assistance\nReferral program\nRelocation assistance\nVision insurance\nEducation:\nBachelor's (Required)\nAbility to Relocate:\nHerndon, VA 20170: Relocate before starting work (Required)\nWork Location: In person","company":"Validationassociatesllc1","rawCompany":"validationassociatesllc1","city":"Reston","state":"VA","isRemote":false,"isActive":false,"createdAt":"2026-07-18T17:07:18.867Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"},{"code":"17-2199.00","title":"Engineers, All Other","slug":"engineers-all-other"}],"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":"541990","title":"All Other Professional, Scientific, and Technical Services","slug":"all-other-professional-scientific-and-technical-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Validation Engineer (OPT/CPT)","description":"Are you a talented Validation Engineer seeking new opportunities in the US? Join Validation Associates LLC, a specialist pharmaceutical recruitment & staffing consultancy, focused on providing expert services in the life sciences industry.\nResponsibilities:\nPerform equipment qualification, process validation, and cleaning validation activities.\nDevelop and execute validation protocols, including IQ/OQ/PQ.\nConduct risk assessments, root cause analysis, and failure mode effects analysis (FMEA).\nCollaborate with cross-functional teams to ensure compliance with regulatory standards.\nMaintain accurate documentation and reports related to validation activities.\nStay updated on industry regulations and guidelines.\nRequirements:\nBachelors or Master's degree in Engineering, Life Sciences, or related field.\nPrevious experience in validation activities within the pharmaceutical or medical device industry.\nFamiliarity with regulatory guidelines, including FDA regulations and 21 CFR Part 11.\nStrong problem-solving and analytical skills.\nKnowledge of GMP, GDP, and quality systems.\nProficiency in validation software and tools.\nExcellent communication and teamwork abilities.\nBenefits:\nCompetitive compensation package.\nExciting opportunities in the life sciences industry.\nContinuous professional development and training programs.\nCollaborative and supportive work environment.\nCareer growth and advancement opportunities.\nJob Type: Contract\nPay: $30.00 - $33.00 per hour\nBenefits:\n401(k)\n401(k) matching\nDental insurance\nEmployee assistance program\nHealth insurance\nLife insurance\nPaid time off\nProfessional development assistance\nReferral program\nRelocation assistance\nVision insurance\nEducation:\nBachelor's (Required)\nAbility to Relocate:\nHerndon, VA 20170: Relocate before starting work (Required)\nWork Location: In person","datePosted":"2026-07-18T17:07:18.867Z","dateModified":"2026-07-18T17:07:18.867Z","hiringOrganization":{"@type":"Organization","name":"Validationassociatesllc1","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Reston","addressRegion":"VA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"83acef2cbd8f6534174a1f82"},"url":"https://jobsearcher.com/jobs/83acef2cbd8f6534174a1f82"}}