{"schemaVersion":"jobsearcher.job.v1","id":"682d13559f302cac1eded5aa","url":"https://jobsearcher.com/jobs/682d13559f302cac1eded5aa","canonicalUrl":"https://jobsearcher.com/jobs/682d13559f302cac1eded5aa","title":"Packaging Engineer","description":"Now\n\nWe are the people who give possibilities purpose\nBD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.\nJob Description\nThe Packaging Engineer is responsible for the design, development, validation, implementation, and continuous improvement of packaging systems for medical devices manufactured at the site. This role ensures packaging solutions meet product protection, regulatory, quality, operational, and customer requirements while supporting FDA remediation activities, process optimization, product launches, and cost reduction initiatives. The Packaging Engineer collaborates closely with Manufacturing, Quality, R&D, Regulatory Affairs, Supply Chain, and external suppliers to deliver compliant and efficient packaging solutions.\nResponsibilities include but are not limited to:\nPackaging Design & Development\nDesign, develop, and implement primary, secondary, and tertiary packaging systems for medical device products.\nEvaluate packaging materials, components, and configurations to ensure product protection and performance throughout the product lifecycle.\nSupport new product introductions (NPI), product transfers, and packaging changes.\nDevelop packaging specifications, drawings, bill of materials (BOMs), and technical documentation.\nValidation & Regulatory Compliance\nDevelop and execute packaging validation protocols, including:\nInstallation Qualification (IQ)\nOperational Qualification (OQ)\nPerformance Qualification (PQ)\nSupport packaging process validation activities in compliance with:\nFDA Quality System Regulations (21 CFR Part 820)\nISO 13485\nISO 11607\nGood Manufacturing Practices (GMP)\nParticipate in risk assessments, FMEAs, and design reviews.\nEnsure compliance with BD quality standards and documentation requirements.\nManufacturing Support\nProvide engineering support for packaging operations and manufacturing processes.\nInvestigate packaging-related quality issues and implement corrective and preventive actions (CAPA).\nLead root cause investigations using structured problem-solving methodologies.\nSupport nonconformance investigations and continuous improvement initiatives.\nPartner with operations teams to improve packaging efficiency, quality, and productivity.\nContinuous Improvement\nIdentify and execute cost reduction and process improvement opportunities.\nUtilize Lean Manufacturing and Six Sigma tools to improve packaging performance.\nDrive initiatives related to waste reduction, material optimization, and operational excellence.\nSupport digitalization and automation opportunities within packaging processes.\nCross-Functional Collaboration\nCollaborate with R&D, Product Development, Quality Assurance, Regulatory Affairs, Supply Chain, Procurement, and Manufacturing teams.\nInterface with packaging material suppliers and contract manufacturers.\nSupport internal and external audits, including FDA inspections and customer audits.\nProvide technical expertise on packaging-related projects and change controls.\nEducation & Experience\nBachelor’s degree in Packaging Engineering, Mechanical Engineering, Industrial Engineering, Manufacturing Engineering, Biomedical Engineering, or related technical field.\n3+ years of engineering experience in packaging, manufacturing, medical device, pharmaceutical, or highly regulated industries.\nExperience with packaging validation and testing methodologies.\nExperience supporting manufacturing operations and quality systems.\nBilingual (English/Spanish) preferred.\nTechnical Skills\nPackaging materials and technologies\nPackaging equipment and automation systems\nFDA regulations and GMP requirements\nStatistical analysis and validation methodologies\nRisk management and FMEA processes\nRoot cause analysis and CAPA systems\nMicrosoft Office Suite\nSAP, Oracle, or similar ERP systems\nStatistical software (Minitab preferred)\nCAD software preferred\nKey Competencies\nStrong analytical and problem-solving skills.\nExcellent project management abilities.\nEffective verbal and written communication skills.\nAbility to influence cross-functional teams.\nStrong organizational and documentation skills.\nResults-oriented with a continuous improvement mindset.\nAbility to work in manufacturing and cleanroom environment\nWhy Join Us?\nTo find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you’ll discover a culture in which you can learn, grow and thrive.\nWe believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.\nTo learn more about BD visithttps://bd.com/careers.\nBecton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.\nRequired Skills\nOptional Skills\n.\nPrimary Work Location\nUSA TX - El Paso - Northwestern Dr.\nAdditional Locations\nWork Shift","company":"BD","rawCompany":"bd","city":"El Paso","state":"TX","isRemote":false,"isActive":false,"createdAt":"2026-08-09T11:12:05.845Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"17-2141.00","title":"Mechanical Engineers","slug":"mechanical-engineers"},{"code":"17-2112.03","title":"Manufacturing Engineers","slug":"manufacturing-engineers"}],"industries":[{"code":"334510","title":"Electromedical and Electrotherapeutic Apparatus Manufacturing","slug":"electromedical-and-electrotherapeutic-apparatus-manufacturing"},{"code":"339113","title":"Surgical Appliance and Supplies Manufacturing","slug":"surgical-appliance-and-supplies-manufacturing"},{"code":"339112","title":"Surgical and Medical Instrument Manufacturing","slug":"surgical-and-medical-instrument-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Packaging Engineer","description":"Now\n\nWe are the people who give possibilities purpose\nBD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.\nJob Description\nThe Packaging Engineer is responsible for the design, development, validation, implementation, and continuous improvement of packaging systems for medical devices manufactured at the site. This role ensures packaging solutions meet product protection, regulatory, quality, operational, and customer requirements while supporting FDA remediation activities, process optimization, product launches, and cost reduction initiatives. The Packaging Engineer collaborates closely with Manufacturing, Quality, R&D, Regulatory Affairs, Supply Chain, and external suppliers to deliver compliant and efficient packaging solutions.\nResponsibilities include but are not limited to:\nPackaging Design & Development\nDesign, develop, and implement primary, secondary, and tertiary packaging systems for medical device products.\nEvaluate packaging materials, components, and configurations to ensure product protection and performance throughout the product lifecycle.\nSupport new product introductions (NPI), product transfers, and packaging changes.\nDevelop packaging specifications, drawings, bill of materials (BOMs), and technical documentation.\nValidation & Regulatory Compliance\nDevelop and execute packaging validation protocols, including:\nInstallation Qualification (IQ)\nOperational Qualification (OQ)\nPerformance Qualification (PQ)\nSupport packaging process validation activities in compliance with:\nFDA Quality System Regulations (21 CFR Part 820)\nISO 13485\nISO 11607\nGood Manufacturing Practices (GMP)\nParticipate in risk assessments, FMEAs, and design reviews.\nEnsure compliance with BD quality standards and documentation requirements.\nManufacturing Support\nProvide engineering support for packaging operations and manufacturing processes.\nInvestigate packaging-related quality issues and implement corrective and preventive actions (CAPA).\nLead root cause investigations using structured problem-solving methodologies.\nSupport nonconformance investigations and continuous improvement initiatives.\nPartner with operations teams to improve packaging efficiency, quality, and productivity.\nContinuous Improvement\nIdentify and execute cost reduction and process improvement opportunities.\nUtilize Lean Manufacturing and Six Sigma tools to improve packaging performance.\nDrive initiatives related to waste reduction, material optimization, and operational excellence.\nSupport digitalization and automation opportunities within packaging processes.\nCross-Functional Collaboration\nCollaborate with R&D, Product Development, Quality Assurance, Regulatory Affairs, Supply Chain, Procurement, and Manufacturing teams.\nInterface with packaging material suppliers and contract manufacturers.\nSupport internal and external audits, including FDA inspections and customer audits.\nProvide technical expertise on packaging-related projects and change controls.\nEducation & Experience\nBachelor’s degree in Packaging Engineering, Mechanical Engineering, Industrial Engineering, Manufacturing Engineering, Biomedical Engineering, or related technical field.\n3+ years of engineering experience in packaging, manufacturing, medical device, pharmaceutical, or highly regulated industries.\nExperience with packaging validation and testing methodologies.\nExperience supporting manufacturing operations and quality systems.\nBilingual (English/Spanish) preferred.\nTechnical Skills\nPackaging materials and technologies\nPackaging equipment and automation systems\nFDA regulations and GMP requirements\nStatistical analysis and validation methodologies\nRisk management and FMEA processes\nRoot cause analysis and CAPA systems\nMicrosoft Office Suite\nSAP, Oracle, or similar ERP systems\nStatistical software (Minitab preferred)\nCAD software preferred\nKey Competencies\nStrong analytical and problem-solving skills.\nExcellent project management abilities.\nEffective verbal and written communication skills.\nAbility to influence cross-functional teams.\nStrong organizational and documentation skills.\nResults-oriented with a continuous improvement mindset.\nAbility to work in manufacturing and cleanroom environment\nWhy Join Us?\nTo find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you’ll discover a culture in which you can learn, grow and thrive.\nWe believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.\nTo learn more about BD visithttps://bd.com/careers.\nBecton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.\nRequired Skills\nOptional Skills\n.\nPrimary Work Location\nUSA TX - El Paso - Northwestern Dr.\nAdditional Locations\nWork Shift","datePosted":"2026-08-09T11:12:05.845Z","dateModified":"2026-08-09T11:12:05.845Z","hiringOrganization":{"@type":"Organization","name":"BD","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"El Paso","addressRegion":"TX","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"682d13559f302cac1eded5aa"},"url":"https://jobsearcher.com/jobs/682d13559f302cac1eded5aa"}}