Senior Engineering Manager - Automation & Equipment Development

Dexcom

Mesa (AZ)

On-site

USD 149,000 - 248,000

Full time

10 days ago
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Benefits offered by this job

Comprehensive benefits program
Global growth opportunities
Career development & tuition support
Access to cutting-edge CGM technology

Job summary

Dexcom is seeking a senior engineering leader to drive automation and equipment development for sensor manufacturing. You will lead a high-performing team, translate process requirements into detailed equipment specs, and ensure robust, compliant execution across sites.

The role emphasizes lifecycle ownership from concept to transfer, with a heavy focus on reliability, yield, and OEE in a regulated medical device environment.

Qualifications

  • Typically requires a Bachelor’s degree with 13+ years of industry experience.
  • Strong leadership experience in high-volume, regulated manufacturing environments.
  • Experience with NPI, capacity expansion, and technology transitions.

Responsibilities

  • Lead a high-performing engineering team responsible for automation and equipment development.
  • Plan, scope, and prioritize projects across sites to meet timelines.
  • Translate requirements into URS, validation protocols, and compliant docs.
  • Drive equipment lifecycle from concept to transfer to manufacturing.
  • Collaborate with Manufacturing, R&D, Quality to deploy across sites.
  • Drive continuous improvement for yield, throughput, and OEE.

Skills

Automation leadership
Team leadership
Data-driven decision making
Project management
Manufacturing process optimization
Problem-solving

Education

Bachelor’s degree in a technical discipline

Tools

Robotics
PLC programming
Vision systems
Equipment qualification
Process validation

Job description

Dexcom is seeking a senior engineering leader to drive automation and equipment development for sensor manufacturing. You will lead a high-performing team, translate process requirements into detailed equipment specs, and ensure robust, compliant execution across sites.

The role emphasizes lifecycle ownership from concept to transfer, with a heavy focus on reliability, yield, and OEE in a regulated medical device environment.

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