Packaging Engineering at Apptad Inc Georgia

Sunseeker Property Service

Tybee Island (GA)

On-site

USD 85,000 - 120,000

Full time

14 days+

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Job summary

Becton, Dickinson is seeking a Packaging Engineer in El Paso, TX to design, develop, validate, and implement packaging systems for medical devices, ensuring product protection, regulatory compliance, and cost effectiveness throughout the lifecycle.

This role collaborates with Manufacturing, Quality, R&D, Regulatory Affairs, and Supply Chain to support NPI, product transfers, changes, and a variety of audits, while leading packaging validation efforts (IQ/OQ/PQ) under 21 CFR 820, ISO 13485, and

Qualifications

  • Bachelor's degree in Packaging Engineering, Mechanical Engineering, Industrial Engineering, Manufacturing Engineering, Biomedical Engineering, or related field.
  • 3+ years of engineering experience in packaging, manufacturing, medical device, pharmaceutical, or regulated industries.
  • Experience with packaging validation and testing methodologies.
  • Experience supporting manufacturing operations and quality systems.
  • Bilingual (English/Spanish) preferred.

Responsibilities

  • Design, develop, and implement primary, secondary, and tertiary packaging systems for medical device products.
  • Evaluate materials, components, and configurations to ensure product protection and performance.
  • Support NPI, product transfers, and packaging changes.
  • Develop packaging specs, BOMs, and technical documentation.
  • Lead IQ/OQ/PQ validation activities and regulatory compliance tasks.
  • Investigate packaging-related quality issues and drive CAPA.
  • Collaborate with Manufacturing, Quality, R&D, Regulatory Affairs, and Supply Chain.

Skills

Packaging materials
Packaging equipment
FDA GMP
Statistical analysis
FMEA
CAPA
MS Office
ERP systems
Minitab
CAD software

Education

BS in Packaging/Mechanical/Industrial Engineering

Tools

SAP
Oracle
Minitab
CAD software

Job description

Role- Packaging Engineer Location-El Paso, TX Client: HCL/ End client: Becton, Dickinson

JOB DESCRIPTION:

Required Qualifications

The 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 & Development
  • Design, 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 Compliance

Develop 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 Support
  • Provide 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 Improvement
  • Identify 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 Collaboration
  • Collaborate 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 & Experience

Bachelor'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 Skills
  • Packaging 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 systems
  • Microsoft Office Suite
  • SAP, Oracle, or similar ERP systems
  • Statistical software (Minitab preferred)
  • CAD software preferred
Key Competencies
  • Strong 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 environment
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