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Manufacturing Operations Quality Engineer

Medtronic

Engineering Jobs

Manufacturing Operations Quality Engineer

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

As a Quality Engineer in Manufacturing, you will play a key role in ensuring that products are manufactured in compliance with internal quality standards, regulatory requirements, and Medtronic’s commitment to patient safety and product excellence. This position partners closely with Manufacturing, Operations, R&D, and Supply Chain to drive quality improvements and support continuous improvement initiatives on the production floor.

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

  • Provide quality engineering support for manufacturing operations and engineering.
  • Support production, engineering, validation activities including training, reviewing and approving documentation, work instructions, SOPs , supporting risk assessments, to ensure compliance with regulatory and quality system requirements.
  • Lead and support investigations of nonconformances, deviations, and CAPAs, including root cause analysis and implementation of corrective and preventive actions.
  • Collaborate with cross-functional teams to identify, assess, and mitigate quality risks in manufacturing processes.
  • Support internal and external audits, including preparation, participation, and follow-up on audit findings.
  • Drive continuous improvement initiatives using quality and lean methodologies.
  • Ensure effective implementation and monitoring of process controls and quality metrics.
  • Support change management activities ensuring requirements are identified and executed when applicable.
  • Participate in Management Review and Quality Metrics reporting.

Required Knowledge and Experience:

  • Bachelor’s degree in Engineering, Biotechnology, Life Sciences, or a related field.
  • Minimum of 7 years of experience in quality engineering or quality assurance of production in medical devices or pharmaceuticals.
  • Knowledge of quality systems and regulatory requirements (e.g., ISO 13485, FDA QMSR, MDR).
  • Strong analytical and problem-solving skills.
  • Ability to work effectively in a cross-functional, fast-paced manufacturing environment.
  • Hands-on experience with ECO’s, nonconformance management, CAPA, and root cause analysis tools.
  • Familiarity with statistical tools and data analysis.
  • Experience supporting audits and inspections.
  • Knowledge of Lean, Six Sigma, or continuous improvement methodologies- advantage.
  • Strong communication skills in English, both written and verbal.

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

  • Yoqneam Illit, North, Israel

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

  • Strong analytical and problem-solving skillsintermediate
  • Ability to work effectively in a cross-functional, fast-paced manufacturing environmentintermediate
  • Hands-on experience with ECO’s, nonconformance management, CAPA, and root cause analysis toolsintermediate
  • Familiarity with statistical tools and data analysisintermediate
  • Experience supporting audits and inspectionsintermediate
  • Knowledge of Lean, Six Sigma, or continuous improvement methodologiesintermediate
  • Strong communication skills in English, both written and verbalintermediate

Required Qualifications

  • Bachelor’s degree in Engineering, Biotechnology, Life Sciences, or a related field (experience)
  • Minimum of 7 years of experience in quality engineering or quality assurance of production in medical devices or pharmaceuticals (experience)
  • Knowledge of quality systems and regulatory requirements (e.g., ISO 13485, FDA QMSR, MDR) (experience)

Responsibilities

  • Provide quality engineering support for manufacturing operations and engineering
  • Support production, engineering, validation activities including training, reviewing and approving documentation, work instructions, SOPs, supporting risk assessments, to ensure compliance with regulatory and quality system requirements
  • Lead and support investigations of nonconformances, deviations, and CAPAs, including root cause analysis and implementation of corrective and preventive actions
  • Collaborate with cross-functional teams to identify, assess, and mitigate quality risks in manufacturing processes
  • Support internal and external audits, including preparation, participation, and follow-up on audit findings
  • Drive continuous improvement initiatives using quality and lean methodologies
  • Ensure effective implementation and monitoring of process controls and quality metrics
  • Support change management activities ensuring requirements are identified and executed when applicable
  • Participate in Management Review and Quality Metrics reporting

Benefits

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

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Medtronic logo

Manufacturing Operations Quality Engineer

Medtronic

Engineering Jobs

Manufacturing Operations Quality Engineer

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

As a Quality Engineer in Manufacturing, you will play a key role in ensuring that products are manufactured in compliance with internal quality standards, regulatory requirements, and Medtronic’s commitment to patient safety and product excellence. This position partners closely with Manufacturing, Operations, R&D, and Supply Chain to drive quality improvements and support continuous improvement initiatives on the production floor.

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

  • Provide quality engineering support for manufacturing operations and engineering.
  • Support production, engineering, validation activities including training, reviewing and approving documentation, work instructions, SOPs , supporting risk assessments, to ensure compliance with regulatory and quality system requirements.
  • Lead and support investigations of nonconformances, deviations, and CAPAs, including root cause analysis and implementation of corrective and preventive actions.
  • Collaborate with cross-functional teams to identify, assess, and mitigate quality risks in manufacturing processes.
  • Support internal and external audits, including preparation, participation, and follow-up on audit findings.
  • Drive continuous improvement initiatives using quality and lean methodologies.
  • Ensure effective implementation and monitoring of process controls and quality metrics.
  • Support change management activities ensuring requirements are identified and executed when applicable.
  • Participate in Management Review and Quality Metrics reporting.

Required Knowledge and Experience:

  • Bachelor’s degree in Engineering, Biotechnology, Life Sciences, or a related field.
  • Minimum of 7 years of experience in quality engineering or quality assurance of production in medical devices or pharmaceuticals.
  • Knowledge of quality systems and regulatory requirements (e.g., ISO 13485, FDA QMSR, MDR).
  • Strong analytical and problem-solving skills.
  • Ability to work effectively in a cross-functional, fast-paced manufacturing environment.
  • Hands-on experience with ECO’s, nonconformance management, CAPA, and root cause analysis tools.
  • Familiarity with statistical tools and data analysis.
  • Experience supporting audits and inspections.
  • Knowledge of Lean, Six Sigma, or continuous improvement methodologies- advantage.
  • Strong communication skills in English, both written and verbal.

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

  • Yoqneam Illit, North, Israel

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

  • Strong analytical and problem-solving skillsintermediate
  • Ability to work effectively in a cross-functional, fast-paced manufacturing environmentintermediate
  • Hands-on experience with ECO’s, nonconformance management, CAPA, and root cause analysis toolsintermediate
  • Familiarity with statistical tools and data analysisintermediate
  • Experience supporting audits and inspectionsintermediate
  • Knowledge of Lean, Six Sigma, or continuous improvement methodologiesintermediate
  • Strong communication skills in English, both written and verbalintermediate

Required Qualifications

  • Bachelor’s degree in Engineering, Biotechnology, Life Sciences, or a related field (experience)
  • Minimum of 7 years of experience in quality engineering or quality assurance of production in medical devices or pharmaceuticals (experience)
  • Knowledge of quality systems and regulatory requirements (e.g., ISO 13485, FDA QMSR, MDR) (experience)

Responsibilities

  • Provide quality engineering support for manufacturing operations and engineering
  • Support production, engineering, validation activities including training, reviewing and approving documentation, work instructions, SOPs, supporting risk assessments, to ensure compliance with regulatory and quality system requirements
  • Lead and support investigations of nonconformances, deviations, and CAPAs, including root cause analysis and implementation of corrective and preventive actions
  • Collaborate with cross-functional teams to identify, assess, and mitigate quality risks in manufacturing processes
  • Support internal and external audits, including preparation, participation, and follow-up on audit findings
  • Drive continuous improvement initiatives using quality and lean methodologies
  • Ensure effective implementation and monitoring of process controls and quality metrics
  • Support change management activities ensuring requirements are identified and executed when applicable
  • Participate in Management Review and Quality Metrics reporting

Benefits

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

Target Your Resume for "Manufacturing Operations Quality Engineer" , Medtronic

Get personalized recommendations to optimize your resume specifically for Manufacturing Operations Quality Engineer. Takes only 15 seconds!

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

Check Your ATS Score for "Manufacturing Operations Quality Engineer" , 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 Manufacturing Operations Quality Engineer @ Medtronic.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.