R&D Engineer II

Medtronic

Remote Actively hiring Posted this week Verified listing
Remote (Usa-Mn Plymouth Berkshire, US) Posted 3 days ago Apply by Jun 22, 2026 $88,800–$133,200 / year
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Market check

Salary context

Below market

How this pay compares to similar roles

Similar $164k
This role $111k
$76k most similar roles pay here $212k

This role pays less than 89% of similar roles. Most pay $128,812–$198,400 — the shaded band above. At the midpoint, this role pays about $111k versus about $164k for comparable roles.

Based on 239 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 51 open roles on FindRole.

Listed pay typically runs $124,800–$187,200 across 50 roles with salary data.

Most-posted roles

View all roles at Medtronic

At a glance

TL;DR

As an Engineer II in Medtronic’s R&D RPM team within the Peripheral Vascular Health Operating Unit, you will support the stents portfolio through product and process development activities, technical documentation, validation efforts, and cross-functional collaboration. Your day-to-day responsibilities include executing test strategies, developing and validating test methods, supporting regulatory submissions, and ensuring compliance with QMS procedures. You will also engage in hands-on laboratory work to deepen your understanding of stent products and manufacturing processes, collaborate on equipment qualification and revalidation activities, and assist with site operational initiatives. The role requires strong technical skills, including familiarity with stent technologies, validation activities, and regulated quality systems, as well as experience with QMS requirements and document control processes. Ideal candidates have a Baccalaureate degree plus two years of relevant engineering experience or a Master’s degree.

Skills

Python SQL QMS ISO 13485 FDA regulations PPAP TMV IQ/OQ/PQ Design Control DFMEA PFMEA DOE Minitab LabVIEW SolidWorks CAD PLM ERP SCADA

What you'll do

  • Support execution of test strategies and completion of testing activities.
  • Perform laboratory work to understand stent products and associated therapies.
  • Execute Test Method Validations in accordance with regulatory requirements.
  • Collaborate on equipment qualification, replacement, and revalidation efforts.
  • Assist cross-functional teams to ensure project timelines and compliance.

What we're looking for

  • 2+ years of engineering experience in medical device or regulated manufacturing industry.
  • Strong technical writing, analytical, and problem-solving skills required.
  • Familiarity with stent technologies, test methods, equipment qualification, and process validation.
  • Experience supporting TMVs, PPAPs, IQ/OQ/PQ activities, and equipment validations.
  • Ability to collaborate across functions for project timelines and compliance requirements.

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