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Supplier Project Manager Electrical

Job in Danvers, Essex County, Massachusetts, 01923, USA
Listing for: Johnson & Johnson
Full Time position
Listed on 2025-12-14
Job specializations:
  • Engineering
    Quality Engineering, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 108800 - 147200 USD Yearly USD 108800.00 147200.00 YEAR
Job Description & How to Apply Below

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and Med Tech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

Learn more at

Job Function:

Supply Chain Engineering

Job Sub Function:

Project Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

US345 MA Danvers - 22 Cherry Hill Dr

Job Description:

Johnson & Johnson Heart Recovery (ABIOMED) is looking to hire a Senior Supplier Project Manager in a hybrid role based in Danvers, MA.

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and Med Tech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

Learn more at

Principle Duties and Responsibilities
  • Lead project management activities for external manufacturing programs

  • Attend product development project meetings and serve as primary liaison for all actions associated with supplier requirements as well as coordinating quality inspection

  • Manage and tracking of supplier related projects for capacity increase, risk mitigation, obsolescence and quality improvement

  • Generate and maintain supply chain program dashboards and report outs for different levels of management

  • Highlight supply chain risks and develop mitigation plans to achieve successful product launches

  • Support the transfer of product improvements into suppliers production utilizing Design for Manufacturing (DFM) principles.

  • Provide project lead for Supplier Engineering team

  • Manage and develop supply chain phase-in plans accounting for various medical device regulatory approval timelines

  • Qualify and implement dimensional and visual inspections through GR&Rs at incoming and Supplier.

  • Assist in the "Quality at the Source" program with the objective of increasing yields at the supplier and qualifying quality inspections at the supplier facility

  • Develop understanding of supplier’s manufacturing process and technology roadmap and capabilities

  • Drive strategic initiatives with suppliers

  • Qualify new suppliers and define necessary technical tests/documentation

  • Perform process validations and verifications of components and sub-assemblies at suppliers.

  • Lead analysis of defective components found in Incoming Inspection and work with vendors to resolve

  • Assist in technical qualification of alternatives for obsolete components

Qualifications:
  • BS in Electrical, Biomedical, or other related Engineering disciplines

  • Successful program management experience, supporting multiple programs in parallel

  • 3+ years of professional experience showing detailed technical exchange with vendors

  • Knowledge of Process Qualifications, Process Capability and data analysis using statistical tools

  • Good knowledge of Six Sigma, Lean and Design of Manufacturing. Six Sigma Green or Black Belt is a +

  • Demonstrated critical thinking in fast paced environment

  • Enjoys working in a team environment while continually and constructively challenging the status quo

  • Basic understanding of medical device regulatory submissions

  • Dedicated, passionate and eager to learn

  • Sound MS Office knowledge

  • Willingness to travel, particularly to visit suppliers (up to 20%)

The anticipated base pay range for this position is $108,800 to $147,200.

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