Senior Packaging Development Leader

6149-DePuy Synthes Products Inc. Legal Entity; Raynham (MA); On-site; USD 105,000 - 182,000; Full time

Benefits offered by this job

Vacation –120 hours per calendar year

Sick time - 40 hours per calendar year

Parental Leave – 480 hours within one年

Job summary

Johnson & Johnson is seeking a packaging design engineering leader to drive end-to-end package developments from concept through commercialization. You will manage portfolios across complex programs, partner with Regulatory Affairs and Product Stewardship, and ensure quality and regulatory readiness for global markets.

The role emphasizes cross-geography collaboration, talent development, and budget-aware execution within the Orthopaedics separation context, with travel up to 10%.

Qualifications

• Bachelor's degree in engineering, business management, or equivalent is required.
• Advanced degree in engineering, business management is preferred.
• 6 - 8+ years of relevant work experience is required.

Responsibilities

• Own end-to-end package design delivery from concept to commercialization.
• Manage multiple projects across stages with PM tools and risk management.
• Interact with senior leadership and partners to set strategic plans and objectives.
• Collaborate with Regulatory Affairs and Label Development to ensure timely compliance.
• Ensure quality output across all phases of package development and supplier inputs.
• Monitor and improve business processes to meet evolving needs.
• Develop team capabilities and manage budget input and prioritization.
• Ensure adherence to Health, Safety and Environmental guidelines.

Skills

Organization and Talent Development

Medical Device knowledge

Experience partnering across geos

New Product Development

Manufacturing Processes

Quality

Education

Bachelor's degree in engineering

Advanced degree preferred

Job description

Johnson & Johnson is seeking a packaging design engineering leader to drive end-to-end package developments from concept through commercialization. You will manage portfolios across complex programs, partner with Regulatory Affairs and Product Stewardship, and ensure quality and regulatory readiness for global markets.

The role emphasizes cross-geography collaboration, talent development, and budget-aware execution within the Orthopaedics separation context, with travel up to 10%.