Medical Devices STEM OPT Jobs in Utah
Utah's medical devices industry spans Salt Lake City, Provo, and the Wasatch Front corridor, with employers like Merit Medical Systems, Nelson Labs, and Natus Medical among active sponsors. F-1 STEM OPT candidates in biomedical engineering, quality systems, and regulatory affairs find consistent demand here, supported by Utah's dense concentration of FDA-registered device manufacturers.
Find Medical Devices JobsOverview
Showing 5 of 11+ Medical Devices STEM OPT Jobs in Utah
See all Medical Devices STEM OPT Jobs in Utah
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Medical Devices STEM OPT Jobs in Utah.
Get Access To All JobsINTRODUCTION
Imagine how your ideas and expertise can change a patient’s life. Our Global Operations & Quality team plays a central part in ensuring our products are delivered to patients with cardiovascular disease. You’ll partner cross-functionally with manufacturing operations and sales teams, delivering thoughtful solutions to complex challenges all while developing your knowledge of the medical device industry. Whether your work includes strategic inventory planning, labeling, warehouse management, material handling, or any of our other supply chain opportunities, you will be making a meaningful contribution to our team and to patients all over the world.
ROLE AND RESPONSIBILITIES
This Senior Engineer will support and sustain the manufacturing of THV delivery systems, with a strong emphasis on continuous improvement. This role involves leading and collaborating with various teams to enhance manufacturing processes, improve product quality, and ensure operational efficiency. Heavy focus will be put on lean manufacturing and continuous improvement.
How you'll make an impact:
- Identify and lead implementation of opportunities to optimize/improve manufacturing processes including using engineering methods (e.g., SIX Sigma and LEAN methods) employing technical design skills to re-design/design of and ensure equipment, tools, fixtures, etc are up to standards
- Develop complex experiments and tests (including writing and executing protocols) to qualify and validate manufacturing processes; analyze results, make recommendations, and develop reports
- Analyze and resolve complex Manufacturing and Compliance issues (e.g., CAPA, non-conformances, audit observations)
- Develop training and documentation materials (e.g., work instructions) for production to enable the seamless knowledge transfer of project and manufacturing processes
- Lead and establish project plans to ensure deliverables are completed to customer’s expectations, using project management tools (e.g., Project Plan, Risk Analysis, etc.)
- Lead and Oversee manufacturing support tasks; give instruction to technicians on conducting tests; train technicians and provide feedback; and coordinate technician work
- Other incidental duties assigned by Leadership
BASIC QUALIFICATIONS
- Bachelor's Degree in Engineering with a minimum of 4 years experience including either industry or industry/education OR
- Master's Degree or equivalent in Engineering with a minimum of 3 years experience including either industry or industry/education OR
- Ph.D. or equivalent in Engineering with industry experience or industry/education
PREFERRED QUALIFICATIONS
- Lean Six Sigma belt certification
- PMP certification
- Experience working in the medical device industry or another highly regulated manufacturing environment
- Experience with Root Cause Analysis (RCA), Nonconformance Reports (NCRs), and Corrective and Preventive Actions (CAPAs)
- Ability to manage multiple priorities and deliver results in a fast-paced manufacturing environment
- Proven ability to work independently and exercise sound engineering judgment
- Proficiency with Microsoft Office Suite, including Excel, PowerPoint, and Project
- Knowledge of applicable FDA regulations and quality system requirements
- Experience with CAPA systems, nonconformance investigations, audit support, change control, and risk management processes
- Experience applying Design of Experiments (DOE), statistical process control (SPC), process capability analysis, and hypothesis testing
- Experience supporting process validation and equipment qualification activities
- Experience leading cross-functional manufacturing improvement projects with measurable business impact
- Experience supporting new product transfers, equipment implementation, or manufacturing technology integration
- Experience working with complex manufacturing equipment and automated production systems
Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.
INTRODUCTION
Imagine how your ideas and expertise can change a patient’s life. Our Global Operations & Quality team plays a central part in ensuring our products are delivered to patients with cardiovascular disease. You’ll partner cross-functionally with manufacturing operations and sales teams, delivering thoughtful solutions to complex challenges all while developing your knowledge of the medical device industry. Whether your work includes strategic inventory planning, labeling, warehouse management, material handling, or any of our other supply chain opportunities, you will be making a meaningful contribution to our team and to patients all over the world.
ROLE AND RESPONSIBILITIES
This Senior Engineer will support and sustain the manufacturing of THV delivery systems, with a strong emphasis on continuous improvement. This role involves leading and collaborating with various teams to enhance manufacturing processes, improve product quality, and ensure operational efficiency. Heavy focus will be put on lean manufacturing and continuous improvement.
How you'll make an impact:
- Identify and lead implementation of opportunities to optimize/improve manufacturing processes including using engineering methods (e.g., SIX Sigma and LEAN methods) employing technical design skills to re-design/design of and ensure equipment, tools, fixtures, etc are up to standards
- Develop complex experiments and tests (including writing and executing protocols) to qualify and validate manufacturing processes; analyze results, make recommendations, and develop reports
- Analyze and resolve complex Manufacturing and Compliance issues (e.g., CAPA, non-conformances, audit observations)
- Develop training and documentation materials (e.g., work instructions) for production to enable the seamless knowledge transfer of project and manufacturing processes
- Lead and establish project plans to ensure deliverables are completed to customer’s expectations, using project management tools (e.g., Project Plan, Risk Analysis, etc.)
- Lead and Oversee manufacturing support tasks; give instruction to technicians on conducting tests; train technicians and provide feedback; and coordinate technician work
- Other incidental duties assigned by Leadership
BASIC QUALIFICATIONS
- Bachelor's Degree in Engineering with a minimum of 4 years experience including either industry or industry/education OR
- Master's Degree or equivalent in Engineering with a minimum of 3 years experience including either industry or industry/education OR
- Ph.D. or equivalent in Engineering with industry experience or industry/education
PREFERRED QUALIFICATIONS
- Lean Six Sigma belt certification
- PMP certification
- Experience working in the medical device industry or another highly regulated manufacturing environment
- Experience with Root Cause Analysis (RCA), Nonconformance Reports (NCRs), and Corrective and Preventive Actions (CAPAs)
- Ability to manage multiple priorities and deliver results in a fast-paced manufacturing environment
- Proven ability to work independently and exercise sound engineering judgment
- Proficiency with Microsoft Office Suite, including Excel, PowerPoint, and Project
- Knowledge of applicable FDA regulations and quality system requirements
- Experience with CAPA systems, nonconformance investigations, audit support, change control, and risk management processes
- Experience applying Design of Experiments (DOE), statistical process control (SPC), process capability analysis, and hypothesis testing
- Experience supporting process validation and equipment qualification activities
- Experience leading cross-functional manufacturing improvement projects with measurable business impact
- Experience supporting new product transfers, equipment implementation, or manufacturing technology integration
- Experience working with complex manufacturing equipment and automated production systems
Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.
STEM OPT Medical Devices Job Roles in Utah
See all Medical Devices STEM OPT Jobs in Utah
Sign up for free to filter by visa type, set job alerts, and find employers with verified sponsorship history.
Search Medical Devices Jobs in UtahMedical Devices STEM OPT Sponsorship Jobs in Utah: Frequently Asked Questions
Which medical devices companies sponsor F-1 STEM OPT visas in Utah?
Merit Medical Systems, based in South Jordan, is one of Utah's largest device manufacturers and has a history of hiring international engineering talent. Nelson Labs, Natus Medical, and Sarcos Technology also operate in the state. Smaller contract manufacturers and OEM suppliers along the Wasatch Front additionally hire STEM OPT candidates in quality, R&D, and manufacturing engineering roles. Sponsorship patterns vary by company size and role type.
Which cities in Utah have the most medical devices F-1 STEM OPT sponsorship jobs?
Salt Lake City and its southern suburbs, including South Jordan and Sandy, account for the highest concentration of medical devices employers in Utah. Provo and Orem in Utah County also host a growing cluster of device and life sciences companies tied to the Provo-Orem tech corridor. Ogden has some manufacturing-focused device employers as well. Most STEM OPT-eligible roles are concentrated in the Salt Lake metro area.
What types of medical devices roles typically qualify for F-1 STEM OPT sponsorship?
Roles requiring a STEM-designated degree are eligible for the 24-month STEM OPT extension. In medical devices, this commonly includes positions in biomedical engineering, mechanical engineering, electrical engineering, quality systems, regulatory affairs, and manufacturing process engineering. Software engineering roles embedded within device development teams may also qualify. The role must align with the student's degree field, and the employer must be enrolled in E-Verify to participate in STEM OPT.
How do I find medical devices F-1 STEM OPT sponsorship jobs in Utah?
Migrate Mate lets you filter specifically for medical devices roles in Utah that are open to F-1 STEM OPT candidates, using verified employer sponsorship data sourced from DOL Labor Condition Application filings. This means you can identify Utah device companies with an actual track record of sponsoring international workers, rather than applying broadly and asking about sponsorship during interviews. Filtering by role type and location helps narrow results to the Wasatch Front employers most active in STEM OPT hiring.
Are there any Utah-specific or industry-specific considerations for F-1 STEM OPT in medical devices?
Utah's medical devices sector is heavily regulated because most products require FDA clearance or approval, which means employers value candidates familiar with quality management systems and regulatory pathways such as 510(k) and PMA. STEM OPT authorization runs for 24 months and requires the employer to be E-Verify enrolled and to file a training plan with your DSO. Utah device manufacturers that sell internationally may also expect familiarity with ISO 13485 standards, which can strengthen a candidate's profile for sponsorship-eligible roles.