{"schemaVersion":"jobsearcher.job.v1","id":"c49c86c95dda9033b75e9d17","url":"https://jobsearcher.com/jobs/c49c86c95dda9033b75e9d17","canonicalUrl":"https://jobsearcher.com/jobs/c49c86c95dda9033b75e9d17","title":"Validation Engineer","description":"Job Title: Validation Engineer\nEmployment Type: Contract\nIndustry: Pharmaceutical\nJob Summary:\nWe are seeking a highly skilled Validation Engineer to join our team in the pharmaceutical industry. In this role, you will be responsible for ensuring that all processes, equipment, systems, and software used in drug production and manufacturing meet the required standards for quality, safety, and compliance. You will develop and execute validation protocols, perform risk assessments, and ensure all validation activities are in accordance with FDA, cGMP, and other relevant regulatory requirements.\nKey Responsibilities:\nDevelop, write, and execute validation protocols (IQ/OQ/PQ) for manufacturing equipment, utilities, processes, and computer systems.\nConduct risk assessments to identify critical parameters and ensure proper validation of equipment and processes.\nSupport the qualification and validation of cleanrooms, HVAC systems, water systems (WFI, purified water), sterilizers, and other critical utilities.\nPerform validation of automated control systems and software, including CSV (Computer System Validation).\nEnsure all validation documentation complies with FDA regulations, cGMP standards, and internal quality systems.\nCollaborate with cross-functional teams, including Quality, Manufacturing, and Engineering, to implement validation activities and corrective actions.\nInvestigate validation deviations and non-conformances, providing technical input for root cause analysis and recommending corrective and preventive actions.\nMaintain and update validation master plans, SOPs, and other validation-related documents.\nParticipate in audits and inspections, providing validation expertise and support.\nStay up-to-date with regulatory changes, technological advancements, and industry best practices related to validation in the pharmaceutical industry.\nQualifications:\nBachelor’s degree in Engineering, Life Sciences, or a related field.\n3-5 years of experience as a Validation Engineer in the pharmaceutical or biotech industry.\nIn-depth knowledge of FDA regulations, cGMP, and pharmaceutical validation processes.\nExperience with IQ/OQ/PQ protocols and validation of equipment, processes, utilities, and software.\nStrong understanding of CSV (Computer System Validation) and GAMP 5 guidelines.\nExcellent problem-solving and troubleshooting skills.\nStrong attention to detail and documentation skills.\nAbility to work in a fast-paced environment and manage multiple projects simultaneously.\nStrong communication and interpersonal skills to collaborate with cross-functional teams.\nPreferred Qualifications:\nExperience with validation of aseptic processing, sterile manufacturing, or biopharmaceutical systems.\nCertification in Validation or Regulatory Affairs.\nFamiliarity with Six Sigma or Lean Manufacturing methodologies.\nJob Type: Contract\nPay: $35.00 - $45.00 per hour\nExpected hours: 8 per week\nSchedule:\n8 hour shift\nWork Location: In person","company":"Kasmo","rawCompany":"kasmo","city":"Plano","state":"TX","isRemote":false,"isActive":false,"createdAt":"2026-08-09T13:47:13.010Z","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":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"},{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Validation Engineer","description":"Job Title: Validation Engineer\nEmployment Type: Contract\nIndustry: Pharmaceutical\nJob Summary:\nWe are seeking a highly skilled Validation Engineer to join our team in the pharmaceutical industry. In this role, you will be responsible for ensuring that all processes, equipment, systems, and software used in drug production and manufacturing meet the required standards for quality, safety, and compliance. You will develop and execute validation protocols, perform risk assessments, and ensure all validation activities are in accordance with FDA, cGMP, and other relevant regulatory requirements.\nKey Responsibilities:\nDevelop, write, and execute validation protocols (IQ/OQ/PQ) for manufacturing equipment, utilities, processes, and computer systems.\nConduct risk assessments to identify critical parameters and ensure proper validation of equipment and processes.\nSupport the qualification and validation of cleanrooms, HVAC systems, water systems (WFI, purified water), sterilizers, and other critical utilities.\nPerform validation of automated control systems and software, including CSV (Computer System Validation).\nEnsure all validation documentation complies with FDA regulations, cGMP standards, and internal quality systems.\nCollaborate with cross-functional teams, including Quality, Manufacturing, and Engineering, to implement validation activities and corrective actions.\nInvestigate validation deviations and non-conformances, providing technical input for root cause analysis and recommending corrective and preventive actions.\nMaintain and update validation master plans, SOPs, and other validation-related documents.\nParticipate in audits and inspections, providing validation expertise and support.\nStay up-to-date with regulatory changes, technological advancements, and industry best practices related to validation in the pharmaceutical industry.\nQualifications:\nBachelor’s degree in Engineering, Life Sciences, or a related field.\n3-5 years of experience as a Validation Engineer in the pharmaceutical or biotech industry.\nIn-depth knowledge of FDA regulations, cGMP, and pharmaceutical validation processes.\nExperience with IQ/OQ/PQ protocols and validation of equipment, processes, utilities, and software.\nStrong understanding of CSV (Computer System Validation) and GAMP 5 guidelines.\nExcellent problem-solving and troubleshooting skills.\nStrong attention to detail and documentation skills.\nAbility to work in a fast-paced environment and manage multiple projects simultaneously.\nStrong communication and interpersonal skills to collaborate with cross-functional teams.\nPreferred Qualifications:\nExperience with validation of aseptic processing, sterile manufacturing, or biopharmaceutical systems.\nCertification in Validation or Regulatory Affairs.\nFamiliarity with Six Sigma or Lean Manufacturing methodologies.\nJob Type: Contract\nPay: $35.00 - $45.00 per hour\nExpected hours: 8 per week\nSchedule:\n8 hour shift\nWork Location: In person","datePosted":"2026-08-09T13:47:13.010Z","dateModified":"2026-08-09T13:47:13.010Z","hiringOrganization":{"@type":"Organization","name":"Kasmo","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Plano","addressRegion":"TX","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"c49c86c95dda9033b75e9d17"},"url":"https://jobsearcher.com/jobs/c49c86c95dda9033b75e9d17"}}