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Quality Engineer II.

Medtronic

Quality Engineer II.

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

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

  • Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product.
  • Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
  • Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.
  • Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.
  • Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.
  • May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality.

TECHNICAL SPECIALIST CAREER STREAM: An individual contributor with responsibility in our technical functions to advance existing technology or introduce new technology and therapies. Formulates, delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. The majority of time is spent delivering R&D, systems or initiatives related to new technologies or therapies – from design to implementation - while adhering to policies, using specialized knowledge and skills.

DIFFERENTIATING FACTORS

Autonomy: Established and productive individual contributor.
Works independently with general supervision on larger, moderately complex projects / assignments.

Organizational Impact: Sets objectives for own job area to meet the objectives of projects and assignments.
Contributes to the completion of project milestones.
May have some involvement in cross functional assignments.

Innovation and Complexity: Problems and issues faced are general, and may require understanding of broader set of issues or other job areas but typically are not complex.
Makes adjustments or recommends enhancements in systems and processes to solve problems or improve effectiveness of job area.

Communication and Influence: Communicates primarily and frequently with internal contacts.
External interactions are less complex or problem solving in nature.
Contacts others to share information, status, needs and issues in order to inform, gain input, and support decision-making.

Leadership and Talent Management: May provide guidance and assistance to entry level professionals and / or employee in Support Career Stream.

Required Knowledge and Experience:

  • Bachelor’s Degree in Industrial Engineering or similar
  • Experience in Medical Industry (+5 Years)
  • Experience in the Quality area (+3 Years)
  • ISO 13485 experience
  • Root Cause Analysis or other problem solving tools
  • Proficient with engineering changes and Equipment Validation
  • NCMR's, TMVS, CAPAs, Supplier Changes
  • Project Management
  • Experience managing high efficiency teams
  • Written and spoken English
  • Lean 6 Sigma knowledge

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

  • Tijuana, Baja California, Mexico

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

  • Root Cause Analysis or other problem solving toolsintermediate
  • Proficient with engineering changes and Equipment Validationintermediate
  • NCMR's, TMVS, CAPAs, Supplier Changesintermediate
  • Project Managementintermediate
  • Experience managing high efficiency teamsintermediate
  • Written and spoken Englishintermediate
  • Lean 6 Sigma knowledgeintermediate

Required Qualifications

  • Bachelor’s Degree in Industrial Engineering or similar (experience)
  • Experience in Medical Industry (+5 Years) (experience)
  • Experience in the Quality area (+3 Years) (experience)
  • ISO 13485 experience (experience)

Responsibilities

  • Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product
  • Collaborates with engineering and manufacturing functions to ensure quality standards are in place
  • Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment
  • Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications
  • Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements
  • May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality

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

Quality Engineer II.

Medtronic

Quality Engineer II.

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

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

  • Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product.
  • Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
  • Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.
  • Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.
  • Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.
  • May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality.

TECHNICAL SPECIALIST CAREER STREAM: An individual contributor with responsibility in our technical functions to advance existing technology or introduce new technology and therapies. Formulates, delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. The majority of time is spent delivering R&D, systems or initiatives related to new technologies or therapies – from design to implementation - while adhering to policies, using specialized knowledge and skills.

DIFFERENTIATING FACTORS

Autonomy: Established and productive individual contributor.
Works independently with general supervision on larger, moderately complex projects / assignments.

Organizational Impact: Sets objectives for own job area to meet the objectives of projects and assignments.
Contributes to the completion of project milestones.
May have some involvement in cross functional assignments.

Innovation and Complexity: Problems and issues faced are general, and may require understanding of broader set of issues or other job areas but typically are not complex.
Makes adjustments or recommends enhancements in systems and processes to solve problems or improve effectiveness of job area.

Communication and Influence: Communicates primarily and frequently with internal contacts.
External interactions are less complex or problem solving in nature.
Contacts others to share information, status, needs and issues in order to inform, gain input, and support decision-making.

Leadership and Talent Management: May provide guidance and assistance to entry level professionals and / or employee in Support Career Stream.

Required Knowledge and Experience:

  • Bachelor’s Degree in Industrial Engineering or similar
  • Experience in Medical Industry (+5 Years)
  • Experience in the Quality area (+3 Years)
  • ISO 13485 experience
  • Root Cause Analysis or other problem solving tools
  • Proficient with engineering changes and Equipment Validation
  • NCMR's, TMVS, CAPAs, Supplier Changes
  • Project Management
  • Experience managing high efficiency teams
  • Written and spoken English
  • Lean 6 Sigma knowledge

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

  • Tijuana, Baja California, Mexico

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

  • Root Cause Analysis or other problem solving toolsintermediate
  • Proficient with engineering changes and Equipment Validationintermediate
  • NCMR's, TMVS, CAPAs, Supplier Changesintermediate
  • Project Managementintermediate
  • Experience managing high efficiency teamsintermediate
  • Written and spoken Englishintermediate
  • Lean 6 Sigma knowledgeintermediate

Required Qualifications

  • Bachelor’s Degree in Industrial Engineering or similar (experience)
  • Experience in Medical Industry (+5 Years) (experience)
  • Experience in the Quality area (+3 Years) (experience)
  • ISO 13485 experience (experience)

Responsibilities

  • Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product
  • Collaborates with engineering and manufacturing functions to ensure quality standards are in place
  • Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment
  • Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications
  • Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements
  • May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality

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 "Quality Engineer II." , Medtronic

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

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

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

10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.