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Packaging Engineer

Becton Dickinson

Packaging Engineer

full-timePosted: Aug 7, 2026Updated: Aug 29, 2026USA TX - El Paso - Northwestern Dr.

Job Description

We are the people who give possibilities purposeBD 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. Job DescriptionThe 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.Responsibilities include but are not limited to:Packaging Design & DevelopmentDesign, develop, and implement primary, secondary, and tertiary packaging systems for medical device products.Evaluate packaging materials, components, and configurations to ensure product protection and performance throughout the product lifecycle.Support new product introductions (NPI), product transfers, and packaging changes.Develop packaging specifications, drawings, bill of materials (BOMs), and technical documentation.Validation & Regulatory ComplianceDevelop and execute packaging validation protocols, including: - Installation Qualification (IQ)-Operational Qualification (OQ)-Performance Qualification (PQ)Support packaging process validation activities in compliance with: -FDA Quality System Regulations (21 CFR Part 820)-ISO 13485-ISO 11607-Good Manufacturing Practices (GMP)Participate in risk assessments, FMEAs, and design reviews.Ensure compliance with BD quality standards and documentation requirements.Manufacturing SupportProvide engineering support for packaging operations and manufacturing processes.Investigate packaging-related quality issues and implement corrective and preventive actions (CAPA).Lead root cause investigations using structured problem-solving methodologies.Support nonconformance investigations and continuous improvement initiatives.Partner with operations teams to improve packaging efficiency, quality, and productivity.Continuous ImprovementIdentify and execute cost reduction and process improvement opportunities.Utilize Lean Manufacturing and Six Sigma tools to improve packaging performance.Drive initiatives related to waste reduction, material optimization, and operational excellence.Support digitalization and automation opportunities within packaging processes.Cross-Functional CollaborationCollaborate with R&D, Product Development, Quality Assurance, Regulatory Affairs, Supply Chain, Procurement, and Manufacturing teams.Interface with packaging material suppliers and contract manufacturers.Support internal and external audits, including FDA inspections and customer audits.Provide technical expertise on packaging-related projects and change controls.Education & ExperienceBachelor’s degree in Packaging Engineering, Mechanical Engineering, Industrial Engineering, Manufacturing Engineering, Biomedical Engineering, or related technical field.3+ years of engineering experience in packaging, manufacturing, medical device, pharmaceutical, or highly regulated industries. Experience with packaging validation and testing methodologies. Experience supporting manufacturing operations and quality systems.Bilingual (English/Spanish) preferred.Technical SkillsPackaging materials and technologies Packaging equipment and automation systems FDA regulations and GMP requirements Statistical analysis and validation methodologies Risk management and FMEA processes Root cause analysis and CAPA systemsMicrosoft Office Suite SAP, Oracle, or similar ERP systems Statistical software (Minitab preferred) CAD software preferred Key CompetenciesStrong analytical and problem-solving skills. Excellent project management abilities. Effective verbal and written communication skills. Ability to influence cross-functional teams. Strong organizational and documentation skills. Results-oriented with a continuous improvement mindset. Ability to work in manufacturing and cleanroom environmentWhy Join Us?To 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. We 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. To learn more about BD visit https://bd.com/careers.Becton, 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.Required SkillsOptional Skills.Primary Work LocationUSA TX - El Paso - Northwestern Dr.Additional LocationsWork Shift

Locations

  • USA TX - El Paso - Northwestern Dr.

Required Qualifications

  • Support packaging process validation activities in compliance with: (experience)
  • Support packaging process validation activities in compliance with: (experience)
  • -FDA Quality System Regulations (21 CFR Part 820) (experience)
  • -Good Manufacturing Practices (GMP) (experience)
  • Participate in risk assessments, FMEAs, and design reviews. (experience)
  • Ensure compliance with BD quality standards and documentation requirements. (experience)
  • Participate in risk assessments, FMEAs, and design reviews. (experience)
  • Ensure compliance with BD quality standards and documentation requirements. (experience)
  • Statistical analysis and validation methodologies (experience)
  • Risk management and FMEA processes (experience)
  • Root cause analysis and CAPA systems (experience)
  • Microsoft Office Suite (experience)
  • SAP, Oracle, or similar ERP systems (experience)

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