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Johnson & Johnson

MSAT Packaging Engineer

Johnson & Johnson

. Support deployment of the JJIMSC supply-chain vision focused on manufacturing-network performance, physical assets, processes, products, technical resources, and cost optimization .

Posted 10/13/2026full-timeTitusville • New Jersey • United StatesMid-LevelSenior💰 $79,000 - $127,650 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in packaging engineering, including design, development, and commercialization of advanced therapy solutions, with a strong focus on cold-chain and non-cold-chain distribution testing. Proven ability to lead multifunctional teams and manage complex projects while ensuring compliance with cGMP standards.

Highest-signal resume keywords
Packaging EngineeringProject ManagementCold-Chain Distribution TestingCGMP ComplianceLean Six Sigma

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Packaging DesignProcess Technology TransferLifecycle ManagementCost OptimizationRoot-Cause AnalysisValidation of Packaging EquipmentSecondary Packaging EngineeringTertiary Packaging EngineeringDistribution StudiesTemperature-Control Qualification
Soft Skills
LeadershipCollaborationProblem-SolvingCommunicationInfluencing Others
Certifications & Qualifications
Project Management Professional (PMP)Lean Six SigmaProcess ExcellenceFPXKepner Tregoe
Industry Keywords
PharmaceuticalsBiologicsMedical DevicesRegulated ProductsManufacturing Processes

Tech Stack

Tools & technologies
PMP

About the role

Key responsibilities & impact
  • Support deployment of the JJIMSC supply-chain vision focused on manufacturing-network performance, physical assets, processes, products, technical resources, and cost optimization
  • Provide Advanced Therapies, distribution studies, shipping-route verification, and packaging subject-matter-expert support
  • Lead and collaborate with multifunctional teams to develop, test, qualify, leverage, and commercialize advanced-therapy solutions
  • Provide secondary and tertiary packaging engineering support for new product launches, technical transfers, and lifecycle management
  • Provide lifecycle packaging equipment, process technology-transfer, and new-product-launch technical support
  • Support commissioning and qualification (C&Q) and process performance validation (PPV/PPQ)
  • Lead physical/simulated distribution testing and temperature-control/cold-chain qualification activities
  • Support product protection studies, packaging-line trials, packaging equipment/material qualifications, child-resistant requirements, human-factor studies, and patient-centric design
  • Support shipping-route verification activities
  • Provide day-to-day secondary and tertiary packaging-material support
  • Investigate packaging-related quality and compliance issues, including equipment assessment, troubleshooting, and root-cause analysis
  • Identify and deliver cost-improvement or cost-avoidance projects and packaging equipment/process efficiency initiatives
  • Design and develop secondary and tertiary packages for equipment performance, process compatibility, and patient/end-user needs
  • Drive leading-edge packaging technology development and implementation across JJIMSC locations
  • Optimize packaging designs, programs, processes, and technical platforms
  • Plan, verify, and control project/program costs and schedules
  • Support sustainable and environmentally friendly packaging initiatives

Requirements

What you’ll need
  • Master's degree in Packaging Engineering or equivalent technical/engineering discipline is required
  • Minimum of six (6) years of related experience in packaging, labeling, and manufacturing processes
  • Project management skills
  • Knowledge in the design, development, testing, qualification, and commercialization of Passive Shipping Solutions
  • Experience with secondary and tertiary packaging materials and designs
  • Knowledge of packaging distribution/transportation testing for cold-chain and non-cold-chain products
  • Knowledge of cGMP
  • Fluent written and spoken English
  • Validation/qualification of packaging equipment, materials, and processes preferred
  • Experience in pharma, chemical, biologics, medical devices, or other regulated products preferred
  • Ability to be effective in a global environment and manage/lead technical issues with multifunctional global partners
  • Ability to lead and influence others in a complex matrix organization preferred
  • Project Management (PMP), Lean Six Sigma, Process Excellence, FPX, and Kepner Tregoe certifications preferred
  • Minimum 20% travel as required by project conditions and business needs

Benefits

Comp & perks
  • Retirement plan (pension)
  • Savings plan (401(k))
  • Vacation – 120 hours per calendar year
  • Sick time – 40 hours per calendar year
  • Holiday pay, including Floating Holidays – 13 days per calendar year
  • Work, Personal and Family Time – up to 40 hours per calendar year
  • Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
  • Bereavement Leave – 240 hours for an immediate family member; 40 hours for an extended family member per calendar year
  • Caregiver Leave – 80 hours in a 52-week rolling period
  • Volunteer Leave – 32 hours per calendar year
  • Military Spouse Time-Off – 80 hours per calendar year
  • Inclusive interview accommodations
  • Equal opportunity employment