Principal Product Engineer - NM - Rice Creek, MN (Onsite)

Medtronic

Quick summary

Work type
On-site
Location
Rice Creek, MN
Salary
$124,000–$186,000 / yr
Posted
2 days ago
Closes
Jul 4, 2026

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $183k
This role $155k
$113k most similar roles pay here $224k

This role pays less than 74% of similar roles. Most pay $152,750–$213,375 — the shaded band above. At the midpoint, this role pays about $155k versus about $183k for comparable roles.

Based on 240 similar postings.

Employer

About Medtronic

Medtronic plc is the world's largest medical technology company by revenue, specializing in device-based therapies for over 70 health conditions.

Medtronic currently has 85 open roles on FindRole.

Listed pay typically runs $122,400–$183,600 across 84 roles with salary data.

Most-posted roles

View all roles at Medtronic

At a glance

TL;DR · Principal Product Engineer - NM - Rice Creek, MN (Onsite)

As Principal Product Engineer in Medtronic’s Neuromodulation Operating Unit, you will lead technical development from feasibility to market release for advanced therapies addressing chronic pain, movement disorders, and neurological conditions. Collaborating with cross-functional teams including engineering, regulatory, marketing, and manufacturing, you will translate clinical needs into product requirements, guide verification and validation activities, and manage risk assessment throughout the lifecycle. Key responsibilities include developing technical strategies, facilitating design decisions, and ensuring seamless integration across development processes. The role requires expertise in electrical, computer, or biomedical engineering with extensive experience in product development, ideally complemented by knowledge of medical device standards like ISO 14708-1 and IEC 60601.

What you'll do

  • Develop and execute technical strategies for product development from feasibility to market release.
  • Translate clinical needs into clear design specifications and requirements.
  • Lead risk assessment and mitigation throughout the product development lifecycle.
  • Facilitate cross-functional communication to drive design decisions and resolve issues.
  • Collaborate with manufacturing partners to ensure alignment on requirements and risks.
  • Establish and oversee design verification plans, ensuring technical rigor in development.

What we're looking for

  • Bachelor’s degree in Electrical, Computer or Biomedical Engineering with at least 7 years of experience.
  • Develop and execute technical strategies for product development from feasibility to market release.
  • Translate clinical needs into clear design specifications and requirements.
  • Identify and mitigate technical risks throughout the product lifecycle.
  • Collaborate with cross-functional teams including manufacturing and suppliers.
  • Facilitate communication and drive decisions in cross-functional settings.

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