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Quality System Specialist

Medtronic

Quality System Specialist

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

Join Medtronic as a Quality Systems Specialist, based in Rolo, Italy and be part of a company dedicated to enhancing people's lives. In this role you will be responsible for ensuring overall implementation of the Quality Management System and compliance within distribution (internal Medtronic and supplier managed).

Medtronic is committed to revolutionizing healthcare to meet the diverse needs of people worldwide. Together, we accelerate the advancement of meaningful innovations, but our success hinges on assembling the right individuals for our team. This is your perfect opportunity to join us and contribute to our mission of engineering the extraordinary.

Responsibilities may include the following and other duties may be assigned:

  • First point of contact on quality topics for processes performed in the local distribution center.
  • Support local stakeholders by building quality knowledge, support detailed process implementation, and use project management / quality tools for continuous improvement of processes.  
  • Manage ISO (International Organization for Standardization) certification activities for the applicable ISO 13485:2016 and provide expertise and guidance in interpreting policies, regulatory and/or governmental regulations, and internal regulations to assure compliance.
  • Use Key Performance Indicators to drive actions and continuous improvement initiatives.
  • Perform internal audits or Gemba Walks to verify process implementation and compliance, working together with operational teams to drive continuous improvement.  
  • Increase awareness on Quality topics and embed a Quality mindset in the organization to put patients first.

Required Knowledge and Experience:

  • Bachelor’s degree in engineering, business management, or similar.
  • Min 2 years of relevant work experience in a highly regulated environment (for example: Pharmaceutical, Medical Technology, Automotive or in a Logistical operational environment).
  • Knowledge and experience with ISO standards (ISO9001 - ISO 13485).
  • Good communication and collaboration skills. 
  • Command of the Italian and English language both verbal and written.

Desirable would be Master’s degree in Engineering, Business Management, or similar.
Also experience in the Medical Device or Pharmaceutical industries would be beneficial.

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.
 

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

  • Rolo, Emilia Romagna, Italy

Salary

Estimated Salary Rangemedium confidence

85,000 - 135,000 USD / yearly

Source: AI Estimation

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Good communication and collaboration skillsintermediate
  • Knowledge and experience with ISO standards (ISO9001 - ISO 13485)intermediate
  • Use project management / quality toolsintermediate
  • Perform internal audits or Gemba Walksintermediate
  • Use Key Performance Indicatorsintermediate

Required Qualifications

  • Bachelor’s degree in engineering, business management, or similar (experience)
  • Min 2 years of relevant work experience in a highly regulated environment (Pharmaceutical, Medical Technology, Automotive or Logistical operational environment) (experience)
  • Command of the Italian and English language both verbal and written (experience)
  • Desirable: Master’s degree in Engineering, Business Management, or similar (experience)
  • Desirable: Experience in the Medical Device or Pharmaceutical industries (experience)

Responsibilities

  • First point of contact on quality topics for processes performed in the local distribution center
  • Support local stakeholders by building quality knowledge, support detailed process implementation, and use project management / quality tools for continuous improvement of processes
  • Manage ISO certification activities for ISO 13485:2016
  • Provide expertise and guidance in interpreting policies, regulatory and/or governmental regulations, and internal regulations to assure compliance
  • Use Key Performance Indicators to drive actions and continuous improvement initiatives
  • Perform internal audits or Gemba Walks to verify process implementation and compliance, working together with operational teams to drive continuous improvement
  • Increase awareness on Quality topics and embed a Quality mindset in the organization to put patients first
  • Ensuring overall implementation of the Quality Management System and compliance within distribution (internal Medtronic and supplier managed)

Benefits

  • general: Competitive Salary
  • general: Flexible Benefits Package
  • general: Wide range of benefits, resources, and competitive compensation plans
  • general: Eligible for short-term incentive called the Medtronic Incentive Plan (MIP)

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Medtronic logo

Quality System Specialist

Medtronic

Quality System Specialist

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

Join Medtronic as a Quality Systems Specialist, based in Rolo, Italy and be part of a company dedicated to enhancing people's lives. In this role you will be responsible for ensuring overall implementation of the Quality Management System and compliance within distribution (internal Medtronic and supplier managed).

Medtronic is committed to revolutionizing healthcare to meet the diverse needs of people worldwide. Together, we accelerate the advancement of meaningful innovations, but our success hinges on assembling the right individuals for our team. This is your perfect opportunity to join us and contribute to our mission of engineering the extraordinary.

Responsibilities may include the following and other duties may be assigned:

  • First point of contact on quality topics for processes performed in the local distribution center.
  • Support local stakeholders by building quality knowledge, support detailed process implementation, and use project management / quality tools for continuous improvement of processes.  
  • Manage ISO (International Organization for Standardization) certification activities for the applicable ISO 13485:2016 and provide expertise and guidance in interpreting policies, regulatory and/or governmental regulations, and internal regulations to assure compliance.
  • Use Key Performance Indicators to drive actions and continuous improvement initiatives.
  • Perform internal audits or Gemba Walks to verify process implementation and compliance, working together with operational teams to drive continuous improvement.  
  • Increase awareness on Quality topics and embed a Quality mindset in the organization to put patients first.

Required Knowledge and Experience:

  • Bachelor’s degree in engineering, business management, or similar.
  • Min 2 years of relevant work experience in a highly regulated environment (for example: Pharmaceutical, Medical Technology, Automotive or in a Logistical operational environment).
  • Knowledge and experience with ISO standards (ISO9001 - ISO 13485).
  • Good communication and collaboration skills. 
  • Command of the Italian and English language both verbal and written.

Desirable would be Master’s degree in Engineering, Business Management, or similar.
Also experience in the Medical Device or Pharmaceutical industries would be beneficial.

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.
 

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

  • Rolo, Emilia Romagna, Italy

Salary

Estimated Salary Rangemedium confidence

85,000 - 135,000 USD / yearly

Source: AI Estimation

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Good communication and collaboration skillsintermediate
  • Knowledge and experience with ISO standards (ISO9001 - ISO 13485)intermediate
  • Use project management / quality toolsintermediate
  • Perform internal audits or Gemba Walksintermediate
  • Use Key Performance Indicatorsintermediate

Required Qualifications

  • Bachelor’s degree in engineering, business management, or similar (experience)
  • Min 2 years of relevant work experience in a highly regulated environment (Pharmaceutical, Medical Technology, Automotive or Logistical operational environment) (experience)
  • Command of the Italian and English language both verbal and written (experience)
  • Desirable: Master’s degree in Engineering, Business Management, or similar (experience)
  • Desirable: Experience in the Medical Device or Pharmaceutical industries (experience)

Responsibilities

  • First point of contact on quality topics for processes performed in the local distribution center
  • Support local stakeholders by building quality knowledge, support detailed process implementation, and use project management / quality tools for continuous improvement of processes
  • Manage ISO certification activities for ISO 13485:2016
  • Provide expertise and guidance in interpreting policies, regulatory and/or governmental regulations, and internal regulations to assure compliance
  • Use Key Performance Indicators to drive actions and continuous improvement initiatives
  • Perform internal audits or Gemba Walks to verify process implementation and compliance, working together with operational teams to drive continuous improvement
  • Increase awareness on Quality topics and embed a Quality mindset in the organization to put patients first
  • Ensuring overall implementation of the Quality Management System and compliance within distribution (internal Medtronic and supplier managed)

Benefits

  • general: Competitive Salary
  • general: Flexible Benefits Package
  • general: Wide range of benefits, resources, and competitive compensation plans
  • general: Eligible for short-term incentive called the Medtronic Incentive Plan (MIP)

Target Your Resume for "Quality System Specialist" , Medtronic

Get personalized recommendations to optimize your resume specifically for Quality System Specialist. Takes only 15 seconds!

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

Check Your ATS Score for "Quality System Specialist" , 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
Quiz Challenge

Answer 10 quick questions to check your fit for Quality System Specialist @ Medtronic.

10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.