{"schemaVersion":"jobsearcher.job.v1","id":"a8e5411db822d73e46bb4151","url":"https://jobsearcher.com/jobs/a8e5411db822d73e46bb4151","canonicalUrl":"https://jobsearcher.com/jobs/a8e5411db822d73e46bb4151","title":"QA Validation Engineer","description":"QA Validation Engineer\r\nLocation: Lenexa, KS\r\nJob Summary and Purpose\r\nThe QA Validation Engineer in Lenexa, KS leads, designs, performs, and reports validation activities on processes, equipment, and systems used in the manufacture of regulated veterinary vaccines for domestic and international markets.\r\nResponsibilities and Key Duties\r\nPrepare and execute protocols including Cycle Development, Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), Engineering Studies (ES), Factory Acceptance Test (FAT), and Site Acceptance Test (SAT).\r\nReview protocol drafts and resolve conflicts or concerns to achieve management pre-approval. Coordinate qualification execution and all aspects of validation projects with Operations, Engineering, Quality Control, and Quality Assurance.\r\nPerform or supervise protocol execution and maintain documentation in compliance with current Good Documentation Practices (GDP). Review, analyze, and compile protocol data and write reports for management review and approval.\r\nPerform and document risk assessments to determine validation strategy and approach. Execute re-qualification (RQ) studies and periodic reviews to ensure equipment, systems, and processes remain in a validated state.\r\nSupport and participate in change control processes for qualified and validated equipment, including refrigerators, freezers, incubators, autoclaves, lyophilizers, bioreactors, fermenters, ovens, ampule filling machines, and related systems. Maintain full understanding of applicable change control procedures.\r\nProvide input to, review, and approve User Requirements Specifications (URS). Write, review, and edit standard operating procedures (SOPs) to align with validation requirements.\r\nProvide input to Engineering on the preparation and execution of Factory Acceptance Tests (FAT) and Site Acceptance Tests (SAT).\r\nResearch equipment and processes to establish parameters and testing methods that meet validation requirements. Support the development of Validation Plans and Schedules.\r\nEnsure processes and products comply with all local, state, and federal regulations. Oversee CGMP compliance and establish systems that identify opportunities for improvement and recommend changes to improve process effectiveness and quality.\r\nPerform all other duties as assigned.\r\nTechnical / Functional Competencies\r\nAbility to perform internal and study audits as a lead and participate in external audits as a member of the audit team.\r\nKnowledge of pharmaceutical development, regulatory requirements, and manufacturing sciences with a global perspective.\r\nKnowledge of quality systems tools with the ability to adapt them to organizational needs and global regulatory requirements (GLP, GCP, GMP).\r\nAbility to validate Excel file programming according to defined objectives.\r\nProficiency in the use of data logging equipment and instruments.\r\nExperience performing risk assessments, investigations, CAPAs, and Aseptic Process Simulations (APS or media fills) preferred.\r\nEducation\r\nBachelor's degree in Engineering, Biotechnology, Biology, or Microbiology with 4+ years of validation experience in a biotech, biological, pharmaceutical, or other GMP-regulated industry.\r\nMasters degree in Engineering, Biotechnology, Biology, or Microbiology with 2+ years of validation experience in a biotech, biological, pharmaceutical, or other GMP-regulated industry.\r\nPhysical Requirements\r\nAbility to read, write legibly, and communicate in English.\r\nVisual inspection capability.\r\nOccasional lifting up to 25 pounds.\r\nTasks frequently require prolonged mental and visual concentration.\r\nTravel Required\r\nNone.\r\nThis job description is intended to convey information essential to understanding the scope, general nature, and level of work performed by job holders. It is not intended to be an exhaustive list of qualifications, skills, duties, responsibilities, or working conditions, nor does it constitute an employment contract. Ceva reserves the right to modify job duties and/or job descriptions at any time to meet business needs.\r\n*VEVRAA Federal Contractor\r\nCeva is an equal opportunity employer and all qualified applicants will be considered for employment without regard to race, color, religion, sex, national origin, age, genetic information, actual or perceived sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law. Ceva encourages men and women, members of all racial and ethnic groups, individuals with disabilities and veterans to apply.\r\n669B\r\nJ-18808-Ljbffr","company":"Ceva Logistics","rawCompany":"ceva logistics","city":"Lenexa","state":"KS","isRemote":false,"isActive":false,"createdAt":"2026-07-16T01:41:51.702Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"},{"code":"15-1253.00","title":"Software Quality Assurance Analysts and Testers","slug":"software-quality-assurance-analysts-and-testers"}],"industries":[{"code":"541330","title":"Engineering Services","slug":"engineering-services"},{"code":"115210","title":"Support Activities for Animal Production","slug":"support-activities-for-animal-production"},{"code":"513210","title":"Software Publishers","slug":"software-publishers"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"QA Validation Engineer","description":"QA Validation Engineer\r\nLocation: Lenexa, KS\r\nJob Summary and Purpose\r\nThe QA Validation Engineer in Lenexa, KS leads, designs, performs, and reports validation activities on processes, equipment, and systems used in the manufacture of regulated veterinary vaccines for domestic and international markets.\r\nResponsibilities and Key Duties\r\nPrepare and execute protocols including Cycle Development, Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), Engineering Studies (ES), Factory Acceptance Test (FAT), and Site Acceptance Test (SAT).\r\nReview protocol drafts and resolve conflicts or concerns to achieve management pre-approval. Coordinate qualification execution and all aspects of validation projects with Operations, Engineering, Quality Control, and Quality Assurance.\r\nPerform or supervise protocol execution and maintain documentation in compliance with current Good Documentation Practices (GDP). Review, analyze, and compile protocol data and write reports for management review and approval.\r\nPerform and document risk assessments to determine validation strategy and approach. Execute re-qualification (RQ) studies and periodic reviews to ensure equipment, systems, and processes remain in a validated state.\r\nSupport and participate in change control processes for qualified and validated equipment, including refrigerators, freezers, incubators, autoclaves, lyophilizers, bioreactors, fermenters, ovens, ampule filling machines, and related systems. Maintain full understanding of applicable change control procedures.\r\nProvide input to, review, and approve User Requirements Specifications (URS). Write, review, and edit standard operating procedures (SOPs) to align with validation requirements.\r\nProvide input to Engineering on the preparation and execution of Factory Acceptance Tests (FAT) and Site Acceptance Tests (SAT).\r\nResearch equipment and processes to establish parameters and testing methods that meet validation requirements. Support the development of Validation Plans and Schedules.\r\nEnsure processes and products comply with all local, state, and federal regulations. Oversee CGMP compliance and establish systems that identify opportunities for improvement and recommend changes to improve process effectiveness and quality.\r\nPerform all other duties as assigned.\r\nTechnical / Functional Competencies\r\nAbility to perform internal and study audits as a lead and participate in external audits as a member of the audit team.\r\nKnowledge of pharmaceutical development, regulatory requirements, and manufacturing sciences with a global perspective.\r\nKnowledge of quality systems tools with the ability to adapt them to organizational needs and global regulatory requirements (GLP, GCP, GMP).\r\nAbility to validate Excel file programming according to defined objectives.\r\nProficiency in the use of data logging equipment and instruments.\r\nExperience performing risk assessments, investigations, CAPAs, and Aseptic Process Simulations (APS or media fills) preferred.\r\nEducation\r\nBachelor's degree in Engineering, Biotechnology, Biology, or Microbiology with 4+ years of validation experience in a biotech, biological, pharmaceutical, or other GMP-regulated industry.\r\nMasters degree in Engineering, Biotechnology, Biology, or Microbiology with 2+ years of validation experience in a biotech, biological, pharmaceutical, or other GMP-regulated industry.\r\nPhysical Requirements\r\nAbility to read, write legibly, and communicate in English.\r\nVisual inspection capability.\r\nOccasional lifting up to 25 pounds.\r\nTasks frequently require prolonged mental and visual concentration.\r\nTravel Required\r\nNone.\r\nThis job description is intended to convey information essential to understanding the scope, general nature, and level of work performed by job holders. It is not intended to be an exhaustive list of qualifications, skills, duties, responsibilities, or working conditions, nor does it constitute an employment contract. Ceva reserves the right to modify job duties and/or job descriptions at any time to meet business needs.\r\n*VEVRAA Federal Contractor\r\nCeva is an equal opportunity employer and all qualified applicants will be considered for employment without regard to race, color, religion, sex, national origin, age, genetic information, actual or perceived sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law. Ceva encourages men and women, members of all racial and ethnic groups, individuals with disabilities and veterans to apply.\r\n669B\r\nJ-18808-Ljbffr","datePosted":"2026-07-16T01:41:51.702Z","dateModified":"2026-07-16T01:41:51.702Z","hiringOrganization":{"@type":"Organization","name":"Ceva Logistics","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Lenexa","addressRegion":"KS","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"a8e5411db822d73e46bb4151"},"url":"https://jobsearcher.com/jobs/a8e5411db822d73e46bb4151"}}