Sr. Manager Product Engineering

Becton, Dickinson, and Company

San Diego, CA, USA
Base: $158,300.00 - $261,100.00 usd annual; bonus/...
Fully remote
10 years r&d technical engineering experience
Deep knowledge of fda and iso 13485 regulations
Experience with design control and risk analysis
This role provides technical leadership and manages both direct and indirect reports within a global medical technology company dedicated to advancing the world of health

Job Summary

  • This role provides technical leadership and manages both direct and indirect reports within a global medical technology company dedicated to advancing the world of health.
  • The successful candidate will implement best-in-class R&D tools and standards while collaborating with functional leaders to assign engineering disciplines for platform goals.
  • BD prioritizes on-site collaboration requiring a minimum of 4 days per week in the office to foster creativity and effective problem-solving.

Matching Summary

This role provides technical leadership and manages both direct and indirect reports within a global medical technology company dedicated to advancing the world of health.

Salary

Base: $158,300.00 - $261,100.00 USD Annual; Bonus/Equity: Not specified; Benefits: Comprehensive Total Rewards program including performance-based culture

Skills & Requirements

Must-have

  • 10 years R&D technical engineering experience
  • Deep knowledge of FDA and ISO 13485 regulations
  • Experience with Design Control and Risk Analysis
  • Proven success in medical device product development
  • Knowledge of Verification and Validation processes

Nice-to-have

  • Foster culture of engineering excellence and innovation
  • Strong communication and organizational change skills
  • Ability to mentor and develop top talent
  • Experience with organic and inorganic development opportunities

Key Requirements

  • Bachelor of Science in Mechanical, Systems, or Biomedical Engineering
  • Minimum 10 years of growing responsibility in R&D roles
  • Regulated industry experience including FDA and ISO 13485
  • Must have knowledge in Design & Development and Risk Analysis

Work Rights

Not specified

Tailored Resume

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