Sr. Development Engineer

Medtronic UK

North Haven, United States
$134,000 to $157,200 py; not specified; health, de...
Surgical robotics verification strategy
Product requirements coordination
Design optimization for manufacturability
Responsible for the Verification Strategy for the Surgical Robotics projects in development, partnering with Systems Engineering, Marketing, design teams, Quality, and Project Management

Job Summary

  • Responsible for the Verification Strategy for the Surgical Robotics projects in development, partnering with Systems Engineering, Marketing, design teams, Quality, and Project Management.
  • Develop and evaluate designs to meet defined product requirements and be optimized for manufacturability, reliability, and overall cost to the business.
  • The company offers a comprehensive benefits package including health, dental, vision insurance, retirement plans, and paid time off.

Matching Summary

Responsible for the Verification Strategy for the Surgical Robotics projects in development, partnering with Systems Engineering, Marketing, design teams, Quality, and Project Management.

Salary

$134,000 to $157,200 per year; Not specified; Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, Simple Steps (global well-being program), Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement, Capital Accumulation Plan

Skills & Requirements

Must-have

  • Surgical Robotics verification strategy
  • product requirements coordination
  • design optimization for manufacturability
  • ISO 13485:2003 and ISO 14971:2007
  • medical device risk activities
  • Good Manufacturing Practices (GMP)
  • statistical tools including Minitab

Nice-to-have

  • partnering with cross-functional teams
  • navigating industry regulations
  • problem-solving and root cause investigation

Key Requirements

  • Master's degree in Engineering
  • 2 years Systems Engineer experience
  • 2 years reviewing product requirements
  • 2 years ISO 13485:2003 and ISO 14971:2007
  • 2 years risk activities and GMP
  • 2 years statistical tools including Minitab
  • 2 years DOE, ANOVA/T-Test, regression analysis, QMS, FDA 21 CFR Part 820
  • 2 years authoring Design Verification protocols and reports
  • 2 years reviewing test methods/procedures
  • 2 years PQ deliverables

Work Rights

Not specified

Tailored Resume

Cover Letter