Technical Program Manager

Johnson & Johnson

Santa Clara, California, United States
Base: $134,000 - $231,150; benefits: medical, dent...
Not specified in the job description.
Endoscopic instrument development
Agile project planning and execution
Technical risk mitigation
Johnson & Johnson is seeking a Technical Program Manager for their Instruments & Accessories Development Team in Santa Clara, CA. The ideal candidate will have extensive experience in medical device development, project management, and a strong ability to lead cross-functional teams

Job Summary

  • This role is responsible for organizing and driving the design and development efforts, timelines, and strategies required to meet Endoscopic Instruments & Accessories project and program goals.
  • Key responsibilities include overseeing execution of various endoscopic instrument development programs, preparing and coordinating engineering project timelines, and ensuring project work meets established objectives.
  • The anticipated base pay range for this position is $134,000 - $231,150, with eligibility for various company-sponsored employee benefit programs.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Technical Program Manager for their Instruments & Accessories Development Team in Santa Clara, CA. The ideal candidate will have extensive experience in medical device development, project management, and a strong ability to lead cross-functional teams.

Salary

Base: $134,000 - $231,150; Benefits: medical, dental, vision, life insurance, disability, retirement plan, 401(k), paid time off

Skills & Requirements

Must-have

  • endoscopic instrument development
  • Agile project planning and execution
  • technical risk mitigation
  • cross-functional team leadership
  • medical device development lifecycle
  • vendor and contract manufacturer management

Nice-to-have

  • high-growth collaborative environment
  • continuous improvement culture
  • can-do demeanor
  • robotically controlled medical devices

Key Requirements

  • BS/MS in Mechanical, Electrical, Biomedical, or related Engineering field
  • 8+ years of product development experience
  • 5+ years of program/project leadership experience
  • Proven experience in regulated medical device development
  • Proficiency with project management tools (Smartsheet, MS Project, Jira)
  • Ability to travel up to 10%

Work Rights

Not specified

Tailored Resume

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