{"schemaVersion":"jobsearcher.job.v1","id":"d979eb32a7d26a5830e69e53","url":"https://jobsearcher.com/jobs/d979eb32a7d26a5830e69e53","canonicalUrl":"https://jobsearcher.com/jobs/d979eb32a7d26a5830e69e53","title":"Validation Engineer","description":"Validation Engineer\nDepartment: R&D and Validation\nThe Validation Engineer is responsible for the regulation and support of equipment and systems. Assists in equipment selection, specification, and negotiating fees. Maintains all records related to qualification and validation. Works on projects where data analysis requires evaluation of defined factors to broad concepts. Utilizes independent judgment within broad parameters to determine an appropriate solution. Prepares validation reports, suggests and assists in determining specifications, and makes recommendations for modifications as necessary. The Validation Engineer reports to the Validation Supervisor.\nEducation/Experience:\nB.S. in science/engineering field and 1 to 2 years of equipment qualification/validation experience\nSkills/Abilities:\nAbility to understand and demonstrate knowledge of Standard Operating Procedures (SOPs).\nDemonstrates knowledge of Good Manufacturing Practice (GMP) and FDA 21 CFR 210/211/820, EU GMP Annex 1, ICH guidelines.\nHands-on experience with Kaye validator and temperature mapping.\nSoft skills such as technical writing, good communication skills, root-cause investigation and cross-functional coordination skills, detail-oriented mindset.\nResponsibilities include, but are not limited to:\nAuthor I/O/PQ protocols, periodic review documents, specifications, SOPs and summary reports.\nMaintain and execute equipment periodic review activities for various\ndepartments equipment and systems including Facilities, Environmental Monitoring, Bioassay, Manufacturing and Quality Control.\nCo-ordinate with various departments and stakeholders to gather information and documentation related to the equipment and systems.\nAssist in specifying and selecting equipment. Maintains all records related to qualification and validation.\nPrepare periodic review and validation summary reports and make recommendations for modifications as necessary.\nInitiate and maintain Deviation and CAPA activities and perform any corrective actions as needed.\nWORK HOURS:\nPosition is full time.\nThis position may require periodic local travel between CEL-SCI Facilities, to contract facilities, and to external Validation providers.\nLOCATION:\nBaltimore & Elkridge, MD\nWe offer competitive salaries, outstanding comprehensive benefits, and Employee Stock Options.\nPlease submit cv/resume and cover letter to careers@cel-sci.com. Reference the job title in the subject line of the email\nDISCLAIMER:\nCEL-SCI Corporation is committed to a policy of equal employment opportunity. CEL-SCI will recruit, hire, train, and promote into all job titles the most qualified individuals, without regard to race, color, creed, protected veteran status or disability, gender, religion, marital status, registered domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, including genetic characteristics, sexual orientation, or any other consideration made unlawful by federal, state, or local laws.","company":"Celscicorporation","rawCompany":"celscicorporation","city":"Baltimore","state":"MD","isRemote":false,"isActive":false,"createdAt":"2026-08-11T14:58:54.803Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"17-2199.00","title":"Engineers, All Other","slug":"engineers-all-other"},{"code":"17-2031.00","title":"Bioengineers and Biomedical Engineers","slug":"bioengineers-and-biomedical-engineers"}],"industries":[{"code":"541715","title":"Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)","slug":"research-and-development-in-the-physical-engineering-and-life-sciences-except-nanotechnology-and-biotechnology"},{"code":"541330","title":"Engineering Services","slug":"engineering-services"},{"code":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Validation Engineer","description":"Validation Engineer\nDepartment: R&D and Validation\nThe Validation Engineer is responsible for the regulation and support of equipment and systems. Assists in equipment selection, specification, and negotiating fees. Maintains all records related to qualification and validation. Works on projects where data analysis requires evaluation of defined factors to broad concepts. Utilizes independent judgment within broad parameters to determine an appropriate solution. Prepares validation reports, suggests and assists in determining specifications, and makes recommendations for modifications as necessary. The Validation Engineer reports to the Validation Supervisor.\nEducation/Experience:\nB.S. in science/engineering field and 1 to 2 years of equipment qualification/validation experience\nSkills/Abilities:\nAbility to understand and demonstrate knowledge of Standard Operating Procedures (SOPs).\nDemonstrates knowledge of Good Manufacturing Practice (GMP) and FDA 21 CFR 210/211/820, EU GMP Annex 1, ICH guidelines.\nHands-on experience with Kaye validator and temperature mapping.\nSoft skills such as technical writing, good communication skills, root-cause investigation and cross-functional coordination skills, detail-oriented mindset.\nResponsibilities include, but are not limited to:\nAuthor I/O/PQ protocols, periodic review documents, specifications, SOPs and summary reports.\nMaintain and execute equipment periodic review activities for various\ndepartments equipment and systems including Facilities, Environmental Monitoring, Bioassay, Manufacturing and Quality Control.\nCo-ordinate with various departments and stakeholders to gather information and documentation related to the equipment and systems.\nAssist in specifying and selecting equipment. Maintains all records related to qualification and validation.\nPrepare periodic review and validation summary reports and make recommendations for modifications as necessary.\nInitiate and maintain Deviation and CAPA activities and perform any corrective actions as needed.\nWORK HOURS:\nPosition is full time.\nThis position may require periodic local travel between CEL-SCI Facilities, to contract facilities, and to external Validation providers.\nLOCATION:\nBaltimore & Elkridge, MD\nWe offer competitive salaries, outstanding comprehensive benefits, and Employee Stock Options.\nPlease submit cv/resume and cover letter to careers@cel-sci.com. Reference the job title in the subject line of the email\nDISCLAIMER:\nCEL-SCI Corporation is committed to a policy of equal employment opportunity. CEL-SCI will recruit, hire, train, and promote into all job titles the most qualified individuals, without regard to race, color, creed, protected veteran status or disability, gender, religion, marital status, registered domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, including genetic characteristics, sexual orientation, or any other consideration made unlawful by federal, state, or local laws.","datePosted":"2026-08-11T14:58:54.803Z","dateModified":"2026-08-11T14:58:54.803Z","hiringOrganization":{"@type":"Organization","name":"Celscicorporation","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Baltimore","addressRegion":"MD","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"d979eb32a7d26a5830e69e53"},"url":"https://jobsearcher.com/jobs/d979eb32a7d26a5830e69e53"}}