Principal R&d Engineer

Medtronic UK

North Haven, United States
$150,000 to $195,600 py
On-site
Electromechanical medical devices
Fmea and risk assessments
Process validation, doe, gage r&r, gd&t
Medtronic UK is seeking a Principal R&D Engineer to support the design and development of electromechanical medical devices within their Surgical Supplies R&D organization. The ideal candidate will have significant experience in product design, regulatory compliance, and engineering processes related to medical devices

Job Summary

  • Responsible for supporting the design and development of products for the Surgical Supplies R&D organization from concept to commercialization.
  • Coordinate Process Validation, DOE (Design of Experiments), Gage R&R (Gage Repeatability & Reproducibility) and GD&T (Geometric Dimensioning and Tolerancing).
  • The following benefits and additional compensation are available to all regular employees: 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 (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).

Matching Summary

Match Score: 85

Medtronic UK is seeking a Principal R&D Engineer to support the design and development of electromechanical medical devices within their Surgical Supplies R&D organization. The ideal candidate will have significant experience in product design, regulatory compliance, and engineering processes related to medical devices.

Salary

$150,000 to $195,600 per year

Skills & Requirements

Must-have

  • electromechanical medical devices
  • FMEA and Risk Assessments
  • Process Validation, DOE, Gage R&R, GD&T
  • failure investigation techniques
  • Injection Molding Processes
  • Finite Element Analysis using Ansys
  • Dynamic mechanism model creations using Creo

Nice-to-have

  • regulatory notifications and submissions
  • 1D and 3D tolerance studies

Key Requirements

  • Masters’ Degree in Mechanical, Industrial, or Biomedical Engineering
  • five (5) years of experience as an R&D engineer
  • five (5) years’ experience with QSR 21 CFR 820, ISO 9001, ISO 13485, IEC 60601 and ISO 14971
  • five (5) years’ experience with Design Verification, IQ, OQ, PQ, Special Process Validations and Test Method Validations
  • five (5) years’ experience with Plastic & Sheet Metal Design & manufacturing Methodology
  • five (5) years’ experience with Plastic & Metal Injection Molding Processes
  • five (5) years’ experience with Finite Element Analysis with ANSYS
  • five (5) years’ experience with Dynamic Mechanism models creation with Creo Software
  • five (5) years’ experience with 1D and 3D Tolerance stacks with CE Tol Software

Work Rights

Not specified

Tailored Resume

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