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Senior Design Quality Engineer - RPE - Mervue

Medtronic

Engineering Jobs

Senior Design Quality Engineer - RPE - Mervue

full-timePosted: Jan 15, 2026

Job Description

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

A Day in the Life

Medtronic

At Medtronic, we value what makes you unique. Be part of a company that thinks differently to solve problems, make progress, and deliver meaningful innovations.

Our Purpose

The Sr. Design Quality Engineer position, supporting Released Product Engineering [RPE] for the Acute Care & Monitoring [ACM] Operating Unit, is one of development, improvement, and innovation, through technical excellence and cross functional collaboration.

If you pride yourself on your problem-solving skills, meticulous attention to detail and passion for quality this may be the role for you. You will be tasked to provide quality engineering support in design and development of medical device products across the Acute Care and Monitoring [ACM] portfolio of products. Facilitating the application of design controls, Risk Management and Change Control processes in the evaluation and release of product changes.

Come for a job, stay for a career!

A Day in The Life Of:

  • Critically review new and modified product designs to determine their impact to existing or new product requirements and their effect on, patient safety, standards compliance, and reliability.
  • Ensure that design changes to existing products are conducted in compliance with Medtronic’s QMS, ISO13485, EU-MDR and the FDA Quality System Regulations.
  • Lead cross-functional teams to develop product risk management files (risk management plan, risk assessments, dFMEA, and risk management report).
  • Assist in the creation of verification and validation test plans, protocols and reports. Review testing and analysis for standards and product requirements compliance.

Key Skills & Experience

  • 4+ years of Quality experience with a Bachelors Degree
  • 2+ years of Quality experience with a Masters Degree
  • Experience in the Medical Device Industry or a similar role.
  • Good verbal and written communication skills through English, including protocol / report development and review.
  • Experience in ISO 13485
  • Experience in Risk Management ISO 14971
  • Working knowledge of IEC standards.
  • Familiar with IEC 60601 and product specific industry standards.
  • Experience of EU-MDR regulations.
  • Experience of verification/validation test plan development.
  • Experience with CAPA and root cause failure analysis.

Nice to have

  • Previous experience in Electronic, PCB design, Hardware.
  • Working knowledge of Electronic Schematics, circuit simulation and analysis, PCB Assembly Drawings.
  • Comparative Statistical techniques, sampling plans, GR&R, K-factor, hypothesis testing, ANOVA, parametric and non-parametric analysis.
  • Familiar with statistical software tools (Minitab, Stat Graphics, Statistical),
  • Stability, Biocompatibility, Sterilization, Ship Testing, HALT/HASS.
  • Familiar with DMAIC or DMADV(DFSS) methodologies.
  • DFSS / Lean Green Belt or Black Belt.

Medtronic offer a competitive salary and flexible Benefits Package

#IJA

Physical Job Requirements

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. 

Benefits & Compensation

Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create.  We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
 

 

Pay range / Rango salarial / Intervalo salarial /Fascia retributiva / Tranche de salaire / Gehaltsband / Salaribereik:  Ireland: 62,320.00 EUR - 93,480.00 EUR | 

 

This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

About Medtronic

We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people. 
We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.

Learn more about our business, mission, and our commitment to diversity here  
 

Locations

  • Galway, County Galway, Ireland

Salary

62,320 - 93,480 EUR / yearly

Skills Required

  • Good verbal and written communication skills through English, including protocol / report development and reviewintermediate
  • Experience in ISO 13485intermediate
  • Experience in Risk Management ISO 14971intermediate
  • Working knowledge of IEC standardsintermediate
  • Familiar with IEC 60601 and product specific industry standardsintermediate
  • Experience of EU-MDR regulationsintermediate
  • Experience of verification/validation test plan developmentintermediate
  • Experience with CAPA and root cause failure analysisintermediate

Required Qualifications

  • 4+ years of Quality experience with a Bachelors Degree (experience)
  • 2+ years of Quality experience with a Masters Degree (experience)
  • Experience in the Medical Device Industry or a similar role (experience)

Responsibilities

  • Critically review new and modified product designs to determine their impact to existing or new product requirements and their effect on, patient safety, standards compliance, and reliability
  • Ensure that design changes to existing products are conducted in compliance with Medtronic’s QMS, ISO13485, EU-MDR and the FDA Quality System Regulations
  • Lead cross-functional teams to develop product risk management files (risk management plan, risk assessments, dFMEA, and risk management report)
  • Assist in the creation of verification and validation test plans, protocols and reports
  • Review testing and analysis for standards and product requirements compliance

Benefits

  • general: competitive Salary
  • general: flexible Benefits Package
  • general: wide range of benefits, resources, and competitive compensation plans
  • general: Medtronic Incentive Plan (MIP)

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Medtronic logo

Senior Design Quality Engineer - RPE - Mervue

Medtronic

Engineering Jobs

Senior Design Quality Engineer - RPE - Mervue

full-timePosted: Jan 15, 2026

Job Description

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

A Day in the Life

Medtronic

At Medtronic, we value what makes you unique. Be part of a company that thinks differently to solve problems, make progress, and deliver meaningful innovations.

Our Purpose

The Sr. Design Quality Engineer position, supporting Released Product Engineering [RPE] for the Acute Care & Monitoring [ACM] Operating Unit, is one of development, improvement, and innovation, through technical excellence and cross functional collaboration.

If you pride yourself on your problem-solving skills, meticulous attention to detail and passion for quality this may be the role for you. You will be tasked to provide quality engineering support in design and development of medical device products across the Acute Care and Monitoring [ACM] portfolio of products. Facilitating the application of design controls, Risk Management and Change Control processes in the evaluation and release of product changes.

Come for a job, stay for a career!

A Day in The Life Of:

  • Critically review new and modified product designs to determine their impact to existing or new product requirements and their effect on, patient safety, standards compliance, and reliability.
  • Ensure that design changes to existing products are conducted in compliance with Medtronic’s QMS, ISO13485, EU-MDR and the FDA Quality System Regulations.
  • Lead cross-functional teams to develop product risk management files (risk management plan, risk assessments, dFMEA, and risk management report).
  • Assist in the creation of verification and validation test plans, protocols and reports. Review testing and analysis for standards and product requirements compliance.

Key Skills & Experience

  • 4+ years of Quality experience with a Bachelors Degree
  • 2+ years of Quality experience with a Masters Degree
  • Experience in the Medical Device Industry or a similar role.
  • Good verbal and written communication skills through English, including protocol / report development and review.
  • Experience in ISO 13485
  • Experience in Risk Management ISO 14971
  • Working knowledge of IEC standards.
  • Familiar with IEC 60601 and product specific industry standards.
  • Experience of EU-MDR regulations.
  • Experience of verification/validation test plan development.
  • Experience with CAPA and root cause failure analysis.

Nice to have

  • Previous experience in Electronic, PCB design, Hardware.
  • Working knowledge of Electronic Schematics, circuit simulation and analysis, PCB Assembly Drawings.
  • Comparative Statistical techniques, sampling plans, GR&R, K-factor, hypothesis testing, ANOVA, parametric and non-parametric analysis.
  • Familiar with statistical software tools (Minitab, Stat Graphics, Statistical),
  • Stability, Biocompatibility, Sterilization, Ship Testing, HALT/HASS.
  • Familiar with DMAIC or DMADV(DFSS) methodologies.
  • DFSS / Lean Green Belt or Black Belt.

Medtronic offer a competitive salary and flexible Benefits Package

#IJA

Physical Job Requirements

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. 

Benefits & Compensation

Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create.  We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
 

 

Pay range / Rango salarial / Intervalo salarial /Fascia retributiva / Tranche de salaire / Gehaltsband / Salaribereik:  Ireland: 62,320.00 EUR - 93,480.00 EUR | 

 

This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

About Medtronic

We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people. 
We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.

Learn more about our business, mission, and our commitment to diversity here  
 

Locations

  • Galway, County Galway, Ireland

Salary

62,320 - 93,480 EUR / yearly

Skills Required

  • Good verbal and written communication skills through English, including protocol / report development and reviewintermediate
  • Experience in ISO 13485intermediate
  • Experience in Risk Management ISO 14971intermediate
  • Working knowledge of IEC standardsintermediate
  • Familiar with IEC 60601 and product specific industry standardsintermediate
  • Experience of EU-MDR regulationsintermediate
  • Experience of verification/validation test plan developmentintermediate
  • Experience with CAPA and root cause failure analysisintermediate

Required Qualifications

  • 4+ years of Quality experience with a Bachelors Degree (experience)
  • 2+ years of Quality experience with a Masters Degree (experience)
  • Experience in the Medical Device Industry or a similar role (experience)

Responsibilities

  • Critically review new and modified product designs to determine their impact to existing or new product requirements and their effect on, patient safety, standards compliance, and reliability
  • Ensure that design changes to existing products are conducted in compliance with Medtronic’s QMS, ISO13485, EU-MDR and the FDA Quality System Regulations
  • Lead cross-functional teams to develop product risk management files (risk management plan, risk assessments, dFMEA, and risk management report)
  • Assist in the creation of verification and validation test plans, protocols and reports
  • Review testing and analysis for standards and product requirements compliance

Benefits

  • general: competitive Salary
  • general: flexible Benefits Package
  • general: wide range of benefits, resources, and competitive compensation plans
  • general: Medtronic Incentive Plan (MIP)

Target Your Resume for "Senior Design Quality Engineer - RPE - Mervue" , Medtronic

Get personalized recommendations to optimize your resume specifically for Senior Design Quality Engineer - RPE - Mervue. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Senior Design Quality Engineer - RPE - Mervue" , Medtronic

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Answer 10 quick questions to check your fit for Senior Design Quality Engineer - RPE - Mervue @ Medtronic.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.