{"schemaVersion":"jobsearcher.job.v1","id":"d7b6b0b4cb2a204ae5ed2de8","url":"https://jobsearcher.com/jobs/d7b6b0b4cb2a204ae5ed2de8","canonicalUrl":"https://jobsearcher.com/jobs/d7b6b0b4cb2a204ae5ed2de8","title":"Compliance Engineer","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:\nCompliance Engineer\nPosition Summary\nThe Compliance Engineer will support capital projects and technical initiatives within regulated pharmaceutical and biotechnology manufacturing environments by supporting quality and compliance activities associated with project execution, engineering operations, and regulated systems.\nThis role is responsible for supporting investigations, CAPA activities, change management coordination, GMP documentation review, compliance tracking, and quality system support activities associated with engineering and project operations.\nThe role requires strong organizational skills, attention to detail, technical writing capabilities, and cross-functional collaboration with Engineering, Operations, Quality, Validation, and project teams within highly regulated environments.\nKey Responsibilities\nSupport investigations, CAPA activities, and quality system documentation associated with project execution and engineering operations.\nSupport tracking and follow-up of change controls, CAPAs, training activities, and compliance-related metrics.\nSupport document reviews, approvals, document routing, and quality system coordination activities.\nAssist with onboarding coordination activities, forms, access requests, and related compliance documentation support.\nSupport tracking and organization of quality records, project documentation, and compliance-related deliverables.\nParticipate in project meetings and support communication of compliance activities, documentation status, risks, and action items.\nSupport continuous improvement initiatives related to quality systems, compliance processes, documentation practices, and operational readiness activities.\nEnsure compliance activities are performed in alignment with applicable GMP requirements, site procedures, and project expectations.\nQualifications & Experience\nBachelor’s degree in Engineering, Science, Business Administration, or related technical field preferred.\nMinimum of 2 years of experience supporting compliance, quality systems, investigations, CAPA, change management, validation, or GMP documentation activities within pharmaceutical, biotechnology, medical device, or other FDA-regulated industries.\nFamiliarity with GMP documentation practices, quality systems, investigations, CAPA processes, change controls, and regulated documentation requirements.\nExperience supporting engineering projects, manufacturing operations, commissioning and qualification activities, or regulated operational environments is preferred.\nFamiliarity with systems such as Kneat, TrackWise, Veeva, Bluebeam, or similar quality and documentation management platforms is preferred.\nExcellent verbal and written communication skills in both English and Spanish, including technical writing, documentation review, and communication with cross-functional teams.\nStrong organizational, analytical, and problem-solving skills with attention to detail and the ability to manage multiple priorities simultaneously.\nAdditional Requirements\nAbility to work on-site in the eastern region of Puerto Rico.\nMust be eligible to complete client-required onboarding, training, and site access requirements.\nAbility to work effectively within fast-paced and highly regulated environments.\nThe above statements describe the general nature and level of work performed and do not represent an exhaustive list of responsibilities.\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":"Gurabo","state":"PR","isRemote":false,"isActive":false,"createdAt":"2026-07-27T13:03:55.565Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"13-1041.00","title":"Compliance Officers","slug":"compliance-officers"},{"code":"11-9199.02","title":"Compliance Managers","slug":"compliance-managers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"541330","title":"Engineering Services","slug":"engineering-services"},{"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":"Compliance Engineer","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:\nCompliance Engineer\nPosition Summary\nThe Compliance Engineer will support capital projects and technical initiatives within regulated pharmaceutical and biotechnology manufacturing environments by supporting quality and compliance activities associated with project execution, engineering operations, and regulated systems.\nThis role is responsible for supporting investigations, CAPA activities, change management coordination, GMP documentation review, compliance tracking, and quality system support activities associated with engineering and project operations.\nThe role requires strong organizational skills, attention to detail, technical writing capabilities, and cross-functional collaboration with Engineering, Operations, Quality, Validation, and project teams within highly regulated environments.\nKey Responsibilities\nSupport investigations, CAPA activities, and quality system documentation associated with project execution and engineering operations.\nSupport tracking and follow-up of change controls, CAPAs, training activities, and compliance-related metrics.\nSupport document reviews, approvals, document routing, and quality system coordination activities.\nAssist with onboarding coordination activities, forms, access requests, and related compliance documentation support.\nSupport tracking and organization of quality records, project documentation, and compliance-related deliverables.\nParticipate in project meetings and support communication of compliance activities, documentation status, risks, and action items.\nSupport continuous improvement initiatives related to quality systems, compliance processes, documentation practices, and operational readiness activities.\nEnsure compliance activities are performed in alignment with applicable GMP requirements, site procedures, and project expectations.\nQualifications & Experience\nBachelor’s degree in Engineering, Science, Business Administration, or related technical field preferred.\nMinimum of 2 years of experience supporting compliance, quality systems, investigations, CAPA, change management, validation, or GMP documentation activities within pharmaceutical, biotechnology, medical device, or other FDA-regulated industries.\nFamiliarity with GMP documentation practices, quality systems, investigations, CAPA processes, change controls, and regulated documentation requirements.\nExperience supporting engineering projects, manufacturing operations, commissioning and qualification activities, or regulated operational environments is preferred.\nFamiliarity with systems such as Kneat, TrackWise, Veeva, Bluebeam, or similar quality and documentation management platforms is preferred.\nExcellent verbal and written communication skills in both English and Spanish, including technical writing, documentation review, and communication with cross-functional teams.\nStrong organizational, analytical, and problem-solving skills with attention to detail and the ability to manage multiple priorities simultaneously.\nAdditional Requirements\nAbility to work on-site in the eastern region of Puerto Rico.\nMust be eligible to complete client-required onboarding, training, and site access requirements.\nAbility to work effectively within fast-paced and highly regulated environments.\nThe above statements describe the general nature and level of work performed and do not represent an exhaustive list of responsibilities.\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":"2026-07-27T13:03:55.565Z","dateModified":"2026-07-27T13:03:55.565Z","hiringOrganization":{"@type":"Organization","name":"Validation","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Gurabo","addressRegion":"PR","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"d7b6b0b4cb2a204ae5ed2de8"},"url":"https://jobsearcher.com/jobs/d7b6b0b4cb2a204ae5ed2de8"}}