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New · posted Oct 27

Medtronic · Medical Devices

Senior Quality Engineer

  • West Valley, UT
  • On-site
  • Full-time
  • Senior & Principal
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EmploymentFull-time
DeadlineCloses Nov 2, 2026

The role

We anticipate the application window for this opening will close on - 2 Nov 2026

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.

What you need

Required Qualifications

  • Bachelor's degree in Engineering, Science, or technical field with 4+ years of engineering and/or quality experience OR Master's degree in Engineering, Science, or technical field with 2+ years of engineering and/or quality experience OR PhD.

Preferred Qualificationsnice to have

  • Bachelor's degree in Chemical Engineering, Biomedical Engineering, Mechanical Engineering, or related engineering discipline; advanced degree preferred.
  • Experience leading process validation activities for complex manufacturing processes in regulated environments.
  • Experience with FDA-regulated medical device or pharmaceutical manufacturing.
  • Experience using statistical analysis tools such as Minitab to support process improvement and quality decision making.
  • Knowledge of Code of Federal Regulations (CFR) requirements, engineering drawings, machining, chemical processing, packaging, and sterilization processes.
  • ASQ Certified Quality Engineer (CQE), Lean Six Sigma certification, or similar quality certification.
  • 2+ years of experience executing process validation activities across the full validation lifecycle.

For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required.

What you'll do

The Operations Quality team partners with manufacturing, engineering, and technical functions to ensure compliance, process capability, product quality, and continuous improvement across manufacturing operations.

This position is based in West Valley, Utah and requires an onsite work schedule five (5) days per week at the manufacturing facility.

As a Senior Quality Engineer, you will provide quality engineering support for manufacturing operations with a primary focus on process validation and quality system execution. This role partners closely with engineering and manufacturing teams to ensure compliant, effective, and sustainable manufacturing processes while driving product quality, process reliability, and regulatory compliance within a highly regulated medical device environment.

  • Lead process validation activities across the full validation lifecycle, including planning, protocol development, execution, analysis, reporting, and ongoing process monitoring.
  • Partner with manufacturing and engineering teams to develop, implement, and maintain quality standards, controls, and manufacturing process requirements.
  • Drive root cause investigations, corrective and preventive actions (CAPA), and nonconforming material (NCMR) activities to resolve quality issues and prevent recurrence.
  • Analyze quality and process performance data using statistical methods to support risk-based decision making and continuous improvement initiatives.
  • Develop and implement inspection, testing, and evaluation methods to verify product quality and manufacturing process capability.
  • Support qualification and validation of manufacturing equipment, processes, and test methods.
  • Ensure quality documentation, validation records, and manufacturing practices comply with applicable regulatory and quality system requirements.
  • Mentor quality and engineering colleagues and provide technical leadership on complex quality and validation projects.

Pay and benefits

$98,400 – $147,600 a year

Employer provided
How this compares

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.

Salary ranges for U.S (excl. PR) locations (USD):$98,400.00 - $147,600.00

This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).

The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).

The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).

Regular employees are those who are not temporary, such as interns.  Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.

Further details are available at the link below:

Medtronic benefits and compensation plans

If you are applying to perform work for Medtronic, Inc. (“Medtronic”) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.

  • Health, dental and vision insurance

  • 401(k) with employer contribution and match

  • Paid time off and paid holidays

  • Employee Stock Purchase Plan

  • Tuition assistance/reimbursement

  • Medtronic Incentive Plan (short-term incentive)

Where you'll work

West Valley, UTOn-siteOpen in Maps (opens in a new tab)

More jobs in West Valley, UT

Working conditions

U.S. Work Authorization & Sponsorship

At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.

Equal opportunity, accessibility and legal noticesMedtronic's statements, word for word

Recruitment Fraud Alert

We are aware of phishing scams targeting job seekers. Please keep the following in mind:

Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.

Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.

If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.

If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at [email protected].

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.

The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.

It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.

Job intelligence

The context around this role

Live data · October 28, 2026

Salary intelligence

How the pay compares

This role's midpoint is 2% above the US median for Validation & CQV roles at this level.

This roleEmployer provided

$98,400 to $147,600 a year

Senior & Principal roles in the US56 roles publishing pay

Middle half $105,375 to $132,250, median $121,000
Annual base pay
Annual base payLowMedianHigh
This role$98,400—$147,600
All US$105,375$121,000$132,250

This role: Medtronic's own published range. Comparisons: the base pay employers published on open Validation & CQV roles at the same level on Regulatory Jobs, October 28, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Validation & CQV

The general path across 123 open Validation & CQV roles on Regulatory Jobs, with the titles they carry most. Not Medtronic's own promotion track.

  1. One step back

    Associate & Specialist

    Often: Associate QA Validation Specialist · Validation Analyst

    $81K median31 open
  2. This role

    Senior & Principal

    Often: Senior Validation Engineer · Engineer III, Validation

    $121K median72 open
  3. Next step

    Manager

    Often: Validation Manager · Manager Quality Assurance Validation

    $135K median13 open
  4. Later

    Director

    Often: Associate Director · Associate Director, Validation

  5. Later

    VP & Executive

    Often: Head of Validation · Head of Validation & Risk Management

Skills DNA

What this role leans on

How many of the posting's 22 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 4 linesLab testing and methods: 3 linesDocumentation and SOPs: 1 lineInvestigations and CAPA: 1 lineValidation and qualification: 7 linesQuality systems and risk: 5 linesCollaboration and leadership: 6 linesGMPLab testingDocumentationInvestigationsValidationQuality systemsTeamwork
  • Validation and qualification7
  • Collaboration and leadership6
  • Quality systems and risk5
  • GMP and compliance4
  • Lab testing and methods3
  • Documentation and SOPs1
  • Investigations and CAPA1

Company hiring pulse

Medtronic on Regulatory Jobs

21
Open roles
17
Distinct roles
11
Locations

By discipline

  • Quality14 67%
  • Regulatory7 33%

By level

  • Senior & Principal15 71%
  • Manager3 14%
  • Associate & Specialist3 14%
See all 21 Medtronic roles

More roles at Medtronic

All 21 Medtronic roles

Similar Validation & CQV roles elsewhere

Senior Quality Engineer at Medtronic

Applications close November 2. $98K–$148K a year, employer provided.

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