{"schemaVersion":"jobsearcher.job.v1","id":"3edcd4ced22713a245d57bd9","url":"https://jobsearcher.com/jobs/3edcd4ced22713a245d57bd9","canonicalUrl":"https://jobsearcher.com/jobs/3edcd4ced22713a245d57bd9","title":"Manufacturing 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 ethical standards for the following position:\nManufacturing Engineer\nRole Summary\nThe Manufacturing Engineer supports enterprise manufacturing operations by assisting with validation activities, documentation generation, manufacturing instructions, data analysis, and process improvement initiatives under the guidance of senior engineering and cross-functional team members.\nKey Responsibilities\nSupport IQ/OQ/PQ and process performance qualification activities by assisting with validation protocols, reports, test execution, and related documentation.\nAssist in developing in-process and receiving inspection systems, basic control plans, sampling plans, and inspection methods for components and manufacturing processes.\nGenerate and maintain equipment documentation, PM/calibration procedures, manufacturing instructions, and process documentation with guidance from senior engineers.\nSupport enterprise manufacturing projects from concept through implementation; participate in cross-functional collaboration with Manufacturing, Quality, R&D, Regulatory, and Supply Chain as applicable.\nApply basic DOE, FMEA/PFMEA, risk analysis, SPC, and root-cause tools to support process characterization, optimization, and improvement.\nSupport Lean Manufacturing and continuous improvement activities focused on yield, cycle time, cost, throughput, and process documentation improvements.\nSupport manufacturing technologies such as laser welding, heat bonding, injection molding, vision systems, fixtures, tooling, test methods, automation, and equipment qualification under technical supervision.\nAssist with CAPA, nonconformance investigations, change control, and product/process scale-up activities as assigned.\nExperience Requirements\nBachelor's degree in Mechanical, Electrical, Industrial, Manufacturing, Biomedical Engineering, or related technical field.\n1-3 years in manufacturing engineering, process engineering, quality engineering, validation, or related technical experience within an FDA-regulated environment preferred.\nBasic working knowledge of 21 CFR Part 820, GMP, ISO 13485, and documentation practices used in regulated manufacturing environments preferred.\nElectrical, mechanical, industrial, or biomedical engineering background applicable to manufacturing systems.\nExposure to automation/controls, tooling, fixtures, test methods, equipment qualification, or process validation preferred.\nFamiliarity with DOE, FMEA/PFMEA, CAPA, root-cause investigation, SPC, and process capability concepts.\nExperience with Microsoft Excel and exposure to Minitab, JMP, or equivalent statistical tools preferred.\nExposure to Lean Manufacturing, Six Sigma, Kaizen, or other continuous improvement methodologies preferred.\nExposure to product introductions, process scale-up, design transfer, or improvements to existing processes preferred.\nStrong analytical, communication, teamwork, technical writing, and problem-solving skills.\nQuality Expectations\nDemonstrates commitment to patient safety and product quality by complying with all applicable quality procedures.\nEnsures proper documentation discipline and supports Quality System compliance with guidance from senior engineers and quality partners.\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":"Dorado","state":"PR","isRemote":false,"isActive":false,"createdAt":"2026-07-31T12:02:23.067Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"17-2112.03","title":"Manufacturing Engineers","slug":"manufacturing-engineers"},{"code":"17-2112.00","title":"Industrial Engineers","slug":"industrial-engineers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"339112","title":"Surgical and Medical Instrument Manufacturing","slug":"surgical-and-medical-instrument-manufacturing"},{"code":"339113","title":"Surgical Appliance and Supplies Manufacturing","slug":"surgical-appliance-and-supplies-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Manufacturing 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 ethical standards for the following position:\nManufacturing Engineer\nRole Summary\nThe Manufacturing Engineer supports enterprise manufacturing operations by assisting with validation activities, documentation generation, manufacturing instructions, data analysis, and process improvement initiatives under the guidance of senior engineering and cross-functional team members.\nKey Responsibilities\nSupport IQ/OQ/PQ and process performance qualification activities by assisting with validation protocols, reports, test execution, and related documentation.\nAssist in developing in-process and receiving inspection systems, basic control plans, sampling plans, and inspection methods for components and manufacturing processes.\nGenerate and maintain equipment documentation, PM/calibration procedures, manufacturing instructions, and process documentation with guidance from senior engineers.\nSupport enterprise manufacturing projects from concept through implementation; participate in cross-functional collaboration with Manufacturing, Quality, R&D, Regulatory, and Supply Chain as applicable.\nApply basic DOE, FMEA/PFMEA, risk analysis, SPC, and root-cause tools to support process characterization, optimization, and improvement.\nSupport Lean Manufacturing and continuous improvement activities focused on yield, cycle time, cost, throughput, and process documentation improvements.\nSupport manufacturing technologies such as laser welding, heat bonding, injection molding, vision systems, fixtures, tooling, test methods, automation, and equipment qualification under technical supervision.\nAssist with CAPA, nonconformance investigations, change control, and product/process scale-up activities as assigned.\nExperience Requirements\nBachelor's degree in Mechanical, Electrical, Industrial, Manufacturing, Biomedical Engineering, or related technical field.\n1-3 years in manufacturing engineering, process engineering, quality engineering, validation, or related technical experience within an FDA-regulated environment preferred.\nBasic working knowledge of 21 CFR Part 820, GMP, ISO 13485, and documentation practices used in regulated manufacturing environments preferred.\nElectrical, mechanical, industrial, or biomedical engineering background applicable to manufacturing systems.\nExposure to automation/controls, tooling, fixtures, test methods, equipment qualification, or process validation preferred.\nFamiliarity with DOE, FMEA/PFMEA, CAPA, root-cause investigation, SPC, and process capability concepts.\nExperience with Microsoft Excel and exposure to Minitab, JMP, or equivalent statistical tools preferred.\nExposure to Lean Manufacturing, Six Sigma, Kaizen, or other continuous improvement methodologies preferred.\nExposure to product introductions, process scale-up, design transfer, or improvements to existing processes preferred.\nStrong analytical, communication, teamwork, technical writing, and problem-solving skills.\nQuality Expectations\nDemonstrates commitment to patient safety and product quality by complying with all applicable quality procedures.\nEnsures proper documentation discipline and supports Quality System compliance with guidance from senior engineers and quality partners.\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":"2026-07-31T12:02:23.067Z","dateModified":"2026-07-31T12:02:23.067Z","hiringOrganization":{"@type":"Organization","name":"Validation","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Dorado","addressRegion":"PR","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"3edcd4ced22713a245d57bd9"},"url":"https://jobsearcher.com/jobs/3edcd4ced22713a245d57bd9"}}