Principal Electrical Engineer - Medical Device Dev

SHPE Houston

Santa Barbara (CA)

On-site

USD 191,000 - 290,000

Full time

5 days ago
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Benefits offered by this job

Medical, Dental and Vision Insurance
Life Insurance
401(k) Retirement Plan Matching
Annual Bonus
Tuition Reimbursement
Paid Time Off

Job summary

Arthrex is seeking a Principal Product Development Engineer to lead the full lifecycle development of cutting-edge medical devices, from concept to market. You will guide cross-functional teams, manage timelines and budgets, and ensure regulatory alignment to drive innovation and patient outcomes.

Ideal candidates have 12+ years in product development, strong CAD skills (Pro/E, SolidWorks), and deep knowledge of FDA/ISO medical device guidelines.

Qualifications

  • Bachelor's degree (or equivalent) in Engineering (Mechanical, Biomedical, Electrical or Software) or Computer Science.
  • 12 Years of experience in product development.
  • MS preferred.

Responsibilities

  • Designs components or systems and modifies existing designs to develop or improve products and manufacturing operations.
  • Leads multifunctional product development teams through feasibility analysis, planning, execution, and budget adherence.
  • Maintains design history files and supports regulatory with technical input as needed.
  • Supports Marketing, Product Management and Manufacturing with technical information for training and process improvements.
  • Travels as needed for trade shows, accounts and–international travel possible.

Skills

Medical device development
Project management
Regulatory knowledge
CAD design (Pro/E/SolidWorks)
Orthopedic anatomy knowledge
Manufacturing awareness

Education

Bachelor's degree in Engineering or CS
MS preferred

Tools

Pro/E
SolidWorks

Job description

Arthrex is seeking a Principal Product Development Engineer to lead the full lifecycle development of cutting-edge medical devices, from concept to market. You will guide cross-functional teams, manage timelines and budgets, and ensure regulatory alignment to drive innovation and patient outcomes.

Ideal candidates have 12+ years in product development, strong CAD skills (Pro/E, SolidWorks), and deep knowledge of FDA/ISO medical device guidelines.

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