Principal Packaging Engineer

Medtronic

Confirmed live 2 days ago High trust
Closes in 5 days Hybrid

Quick summary

Work type
Hybrid
Location
Rice Creek, MNPlymouth, MN
Salary
$124,000–$186,000 / yr
Posted
9 days ago
Freshness
Confirmed live 2 days ago
Closes
Sep 16, 2026 (soon)

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $193k
This role $155k
$110k most similar roles pay here $250k

This role pays less than 88% of similar roles. Most pay $170,000–$216,262 — the shaded band above. At the midpoint, this role pays about $155k versus about $193k 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 47 open roles on FindRole.

Listed pay typically runs $110,400–$165,600 across 45 roles with salary data.

Most-posted roles

View all roles at Medtronic

At a glance

TL;DR · Principal Packaging Engineer

The Principal Packaging Engineer is a key member of the Packaging Development function, where they lead the design, development, and verification of packaging systems for sterile medical devices. This role involves managing projects for both new product development and sustaining engineering initiatives to ensure compliance with regulatory and quality requirements. Day-to-day responsibilities include developing verification strategies, performing shelf-life and biocompatibility testing, evaluating materials, and providing technical mentorship to junior engineers. The candidate will work with technologies and standards including Ethylene Oxide, Steam, and Gamma sterilization methods, while ensuring adherence to FDA, ISO, and ASTM International requirements. This role solves critical challenges in the medical device industry by ensuring that packaging systems maintain product integrity and safety throughout the lifecycle, ultimately ensuring that sterile medical devices are safely delivered to patients.

What you'll do

  • Design, develop, and verify packaging systems for sterile medical devices using Ethylene Oxide, Steam, and Gamma sterilization.
  • Create and execute packaging verification strategies including protocol development, testing, analysis, and technical reporting.
  • Evaluate packaging materials and processes to improve product quality, performance, manufacturability, and regulatory compliance.
  • Manage shelf-life and biocompatibility testing for new material combinations and packaging system changes.
  • Ensure all package designs and validations comply with FDA, ISO, and other industry standards.
  • Serve as a technical liaison for supplier selection, qualification, and material approval activities.
  • Provide technical guidance and mentorship to junior Packaging Engineers and Associate Packaging Engineers.

What we're looking for

  • A Bachelor's degree with 7+ years of professional experience or an advanced degree with 5+ years of professional experience is required.
  • Experience developing, validating, or supporting packaging systems for regulated products is required.
  • Experience authoring technical documentation including protocols, reports, specifications, and validation documentation is required.
  • Experience supporting Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) activities is required.
  • Preferred experience includes 5+ years in the medical device packaging industry or related fields.
  • Familiarity with ISO, ASTM International, and other packaging-related standards is preferred.
  • Working knowledge of project management methodologies and tools is preferred.
  • Work Authorization &amp.

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