Senior Quality Engineer
$98.4k - $147.6kMedtronic
We anticipate the application window for this opening will close on - 13 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 95000 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.
A Day in the Life
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.Primary Responsibilities
- 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.
Required Qualifications
- Bachelors degree in Engineering Science or technical field with 4 years of engineering and/or quality experience OR Masters degree in Engineering Science or technical field with 2 years of engineering and/or quality experience OR PhD.
Preferred Qualifications
- Bachelors 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.
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.
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.
U.S. Work Authorization & Sponsorship
At Medtronic we are committed to fostering an environment where employees can thrive and make a meaningful 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.
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 @ 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 .
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.
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:
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 addition Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
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.
Required Experience:
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