{"schemaVersion":"jobsearcher.job.v1","id":"8cb88db35459308ae090acd3","url":"https://jobsearcher.com/jobs/8cb88db35459308ae090acd3","canonicalUrl":"https://jobsearcher.com/jobs/8cb88db35459308ae090acd3","title":"Specialist Tech Engineering","description":"Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.\nWe are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:\nSpecialist Tech Engineering\nDescription:\nThe Specialist Tech Engineering will provide technical engineering support on all system/equipment optimization strategies, upgrades, replacements, and modifications and ensure that all of the maintenance team operations and activities are maintained in compliance with respect to current corporate policies, industry standards, regulatory standards and FDA standards.\nResponsibilities:\nEnsure utility systems, process maintenance, instrumentation/calibration/electrical systems and technical cleaning systems are maintained in compliance with all applicable industry standards, regulatory standards and FDA standards.\nEnsure the maintenance team training program, standard operating procedures and equipment/system operational standards are consistent throughout the team.\nCoordinate technical support to the maintenance team on engineering issues, regulatory issues, compliance issues, calibration issues, quality issues, microbial/environmental issues, technical cleaning issues, validation issues, electrical issues and process maintenance issues.\nProvide technical support for the maintenance team during FDA and other regulatory agency inspections.\nProvide technical support to the maintenance team in response to the FDA and other regulatory agencies.\nSupport the maintenance team when responding to high purity water systems and environmental monitoring alert/action notifications.\nSupport the investigation on all alert/action notifications. Support the development and maintenance of an audit program for the maintenance team and facilitate routine audits of activities, documentation, operations and related areas to ensure a continued state of compliance.\nAssist plant engineering in the evaluation and implementation of engineering improvements, policy changes, compliance improvements and optimization programs.\nEvaluate sanitization and maintenance procedures.\nPropose changes to the Department Manager.\nPropose modifications for process, utility and clean room systems to the Plant Engineering Group.\nEducation:\nMaster’s degree & 3 years of Engineering experience\nBachelor’s degree & 5 years of Engineering experience\nSkills:\nLeadership and teambuilding,\nVerbal communication.\nWritten Communication/Technical Writing\nComprehensive understanding of validation protocol requirements\nTechnical (Equipment Specific)\nAnalytical Problem Solving Project Management.\nVast experience in Maximo and SAP is required.\nQualifications:\nBachelor's Degree in Science or related field.\nMinimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries.\nExperience in direct process / manufacturing areas.\nMust be fully bilingual (English / Spanish) with excellent oral skills.\nMust be proficient using MS Windows and Microsoft Office applications.\nStrong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.\nTechnical Writing skills and investigations processes.\nAvailable to work extended hours, possibility of weekends and holidays.\nAt Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.\n\nExcited to build something meaningful together? We look forward to hearing from you.\n\nValidation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.","company":"Validation","rawCompany":"validation","city":"Juncos","state":"PR","isRemote":false,"isActive":false,"createdAt":"2026-07-29T11:49:38.275Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"17-2199.00","title":"Engineers, All Other","slug":"engineers-all-other"},{"code":"11-9041.00","title":"Architectural and Engineering Managers","slug":"architectural-and-engineering-managers"}],"industries":[{"code":"541330","title":"Engineering Services","slug":"engineering-services"},{"code":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"},{"code":"334510","title":"Electromedical and Electrotherapeutic Apparatus Manufacturing","slug":"electromedical-and-electrotherapeutic-apparatus-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Specialist Tech Engineering","description":"Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.\nWe are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:\nSpecialist Tech Engineering\nDescription:\nThe Specialist Tech Engineering will provide technical engineering support on all system/equipment optimization strategies, upgrades, replacements, and modifications and ensure that all of the maintenance team operations and activities are maintained in compliance with respect to current corporate policies, industry standards, regulatory standards and FDA standards.\nResponsibilities:\nEnsure utility systems, process maintenance, instrumentation/calibration/electrical systems and technical cleaning systems are maintained in compliance with all applicable industry standards, regulatory standards and FDA standards.\nEnsure the maintenance team training program, standard operating procedures and equipment/system operational standards are consistent throughout the team.\nCoordinate technical support to the maintenance team on engineering issues, regulatory issues, compliance issues, calibration issues, quality issues, microbial/environmental issues, technical cleaning issues, validation issues, electrical issues and process maintenance issues.\nProvide technical support for the maintenance team during FDA and other regulatory agency inspections.\nProvide technical support to the maintenance team in response to the FDA and other regulatory agencies.\nSupport the maintenance team when responding to high purity water systems and environmental monitoring alert/action notifications.\nSupport the investigation on all alert/action notifications. Support the development and maintenance of an audit program for the maintenance team and facilitate routine audits of activities, documentation, operations and related areas to ensure a continued state of compliance.\nAssist plant engineering in the evaluation and implementation of engineering improvements, policy changes, compliance improvements and optimization programs.\nEvaluate sanitization and maintenance procedures.\nPropose changes to the Department Manager.\nPropose modifications for process, utility and clean room systems to the Plant Engineering Group.\nEducation:\nMaster’s degree & 3 years of Engineering experience\nBachelor’s degree & 5 years of Engineering experience\nSkills:\nLeadership and teambuilding,\nVerbal communication.\nWritten Communication/Technical Writing\nComprehensive understanding of validation protocol requirements\nTechnical (Equipment Specific)\nAnalytical Problem Solving Project Management.\nVast experience in Maximo and SAP is required.\nQualifications:\nBachelor's Degree in Science or related field.\nMinimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries.\nExperience in direct process / manufacturing areas.\nMust be fully bilingual (English / Spanish) with excellent oral skills.\nMust be proficient using MS Windows and Microsoft Office applications.\nStrong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.\nTechnical Writing skills and investigations processes.\nAvailable to work extended hours, possibility of weekends and holidays.\nAt Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.\n\nExcited to build something meaningful together? We look forward to hearing from you.\n\nValidation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.","datePosted":"2026-07-29T11:49:38.275Z","dateModified":"2026-07-29T11:49:38.275Z","hiringOrganization":{"@type":"Organization","name":"Validation","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Juncos","addressRegion":"PR","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"8cb88db35459308ae090acd3"},"url":"https://jobsearcher.com/jobs/8cb88db35459308ae090acd3"}}