PD Program Manager

Medtronic

Remote

Quick summary

Work type
Remote
Location
Lafayette Bldg 1
Salary
$163,000–$204,000 / yr
Posted
49 days ago
Closes
Jun 25, 2026

Market check

Salary context

Competitive pay

How this pay compares to similar roles

Similar $177k
This role $184k
$136k most similar roles pay here $229k

This role pays more than 50% of similar roles. Most pay $151,000–$203,325 — the shaded band above. At the midpoint, this role pays about $184k versus about $177k 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 70 open roles on FindRole.

Listed pay typically runs $124,800–$187,200 across 68 roles with salary data.

Most-posted roles

View all roles at Medtronic

At a glance

TL;DR · PD Program Manager

The PD Program Manager role at Medtronic, Inc., is an individual contributor position focused on leading released product management (RPM) programs for energy-based medical devices. This involves providing technical insights to assess the impact of changes on device performance and compliance with regulations such as FDA QSR 21 CFR 820 and ISO standards. The role requires coordinating Voice of Customer activities, conducting formative and summative studies, and utilizing Monte Carlo simulations to manage project risks. Key responsibilities include executing validation protocols (IQ/OQ/PQ), driving system enhancements in SAP environments like S/4HANA and ECC, and overseeing the design and development of precision components for injection molding, extrusion, and CNC machining. The ideal candidate will have a strong background in mechanical or biomedical engineering, experience with FDA regulations, and proficiency in CAD tools such as PTC Creo and SolidWorks, along with DOE and CAPA processes.

What you'll do

  • Provide technical insights on energy-based products to assess impact of changes.
  • Evaluate design and process impacts for remediation efforts addressing field complaints.
  • Coordinate Voice of Customer (VOC) activities and formative studies.
  • Ensure compliance with FDA QSR 21 CFR 820, ISO 13485, and other regulations.
  • Conduct Monte Carlo simulations to assess risks across project phases.
  • Implement validation protocols including Installation Qualification, Operational Qualification, Performance Qualification.
  • Lead design and development of precision components for Injection Molding, Extrusion, CNC Machining.

What we're looking for

  • Bachelor’s degree in relevant engineering field plus 5 years of experience or Master’s degree plus 2 years of experience
  • Minimum 2 years of experience with FDA QSR, ISO standards, and other regulatory requirements
  • Experience using SAP S/4HANA, SAP ECC, and HP ALM for system enhancements and troubleshooting
  • Proficient in CAD tools like PTC Creo, Minitab, SolidWorks, and AutoCAD for design validation
  • Certified Six Sigma Black Belt by ASQ or equivalent certifying agency required
  • Experience with DOE, CAPA process, NCMRs, and tolerance stack-up analysis
  • Ability to collaborate effectively with international team members across different time zones

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