Senior Process Engineer, CGM Manufacturing & Validation

1 DexCom Inc

Mesa (AZ)

On-site

USD 91,000 - 152,000

Full time

14 days+
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Benefits offered by this job

Comprehensive benefits program
Career development opportunities
Global growth opportunities
Tuition reimbursement

Job summary

Dexcom seeks a seasoned engineer to lead cross-functional teams in structured problem solving and data analysis, addressing root causes in CGM manufacturing. You will work hands-on with equipment ranging from manual to automated systems to improve product quality, productivity, and cost efficiency.

You will validate equipment and processes (IQ/OQ/PQ) to meet regulatory and business requirements, collaborating with Regulatory, Quality Assurance, R&D, and Process Engineering to deliver the best

Qualifications

  • Bachelor’s degree in a technical discipline (or higher) is typically required.
  • 5–8 years related experience, or Master’s +2–5 years, or PhD +2–4 years of experience.
  • Travel 5–15% will be required.

Responsibilities

  • Lead cross-functional teams in structured problem solving and data analysis to root cause problems.
  • Hands-on with equipment from manual to automated manufacturing to investigate issues.
  • Design improvements for equipment and processes to improve quality, productivity, and reduce costs.
  • Perform IQ/OQ/PQ validation to ensure equipment meets specs and regulatory requirements.
  • Collaborate with Regulatory, QA, R&D, and Process Engineering to improve patient experience.
  • Write instructions and train technicians on best practices and procedures.

Skills

Structured Problem Solving
DMAIC
DOE
SPC
Team Leadership

Education

Bachelor’s degree in a technical discipline

Job description

Dexcom seeks a seasoned engineer to lead cross-functional teams in structured problem solving and data analysis, addressing root causes in CGM manufacturing. You will work hands-on with equipment ranging from manual to automated systems to improve product quality, productivity, and cost efficiency.

You will validate equipment and processes (IQ/OQ/PQ) to meet regulatory and business requirements, collaborating with Regulatory, Quality Assurance, R&D, and Process Engineering to deliver the best

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