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.
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INTRODUCTION
Ultradent Products Inc, a 47-year dental manufacturing company is seeking out a Quality Engineer I. This person is responsible for ensuring that products meet established quality standards while minimizing quality costs and maximizing customer satisfaction. This role supports product and process quality throughout development, validation, manufacturing, and post-market activities. The Quality Engineer I assists in identifying, documenting, tracking, and resolving quality issues while ensuring compliance with applicable procedures, regulations, and industry standards. This position collaborates cross-functionally with Engineering, Manufacturing, Quality, and Supplier partners to support continuous improvement initiatives, risk management activities, process development, validation efforts, and root cause investigations. The Quality Engineer I compiles and analyzes technical data, prepares reports, and presents findings to stakeholders at all levels of the organization. This position requires onsite presence Monday-Friday in the South Jordan location and will report to the Quality Engineering Manager.
ESSENTIAL DUTIES AND RESPONSIBILITIES
- Participate in product design and process development projects to ensure design controls and manufacturing processes meet quality and regulatory requirements.
- Develop, execute, and document process validations, method validations, and related qualification activities.
- Assist in the design and development of manufacturing processes, inspection methods, measurement systems, and testing tools.
- Support supplier quality initiatives by collaborating with suppliers and Supplier Quality Engineers to improve quality performance and assist with supplier qualification and validation activities.
- Participate in investigations related to customer complaints, corrective and preventive actions (CAPA), nonconformance reports (NCRs), and other quality events.
- Conduct root cause analyses and support implementation of effective corrective actions.
- Assist with internal and external audits as requested by Quality Engineering leadership.
- Partner with Engineering and Manufacturing teams to develop data-driven process controls and identify critical process variables for continuous improvement initiatives.
- Analyze quality and manufacturing data using statistical methods and present findings through technical reports and presentations.
- Support risk management activities and assist senior Quality Engineers with process development and quality improvement projects.
- Complete ongoing technical and quality system training to maintain compliance and professional development.
- Assist in establishing, tracking, and reporting quality metrics and objectives across the organization.
- Support compliance with applicable regulatory and quality system requirements.
REQUIRED KNOWLEDGE AND SKILLS
- Knowledge of quality systems and regulatory requirements, including:
- cGMP
- 21 CFR Parts 210, 211, and 820
- ISO 13485
- ISO 14971
- MDD, MDR, and MDSAP
- Understanding of quality system development, documentation, implementation, and maintenance.
- Basic knowledge of manufacturing statistics and quality engineering tools, including:
- Statistical Process Control (SPC)
- Control Charts
- Root Cause Analysis
- Design of Experiments (DOE)
- Gauge R&R
- Proficiency with Microsoft Office applications.
- Familiarity with Oracle, Agile, Adobe, and Minitab or similar systems.
- Working knowledge of, or willingness to learn, one or more programming languages such as Python, R, SQL, or C++.
- Strong analytical and problem-solving skills.
- Excellent organizational, project management, and time management abilities.
- Ability to work independently while managing multiple priorities.
- Strong written and verbal communication skills, including technical writing and presentation skills.
- Ability to adapt quickly in a dynamic and collaborative environment.
EDUCATION AND EXPERIENCE
Preferred: Bachelor's degree in Engineering, Data Science, Physical Sciences, Life Sciences, or a related technical field from an accredited university.
Academic or professional experience involving technical writing, statistical analysis, and presentation of technical data.
PREFERRED TECHNICAL DISCIPLINES
Candidates should demonstrate proficiency in one or more of the following areas:
- Physics
- Electronics
- Measurement Sciences
- Physical Chemistry
- Analytical Chemistry
- Chemical Engineering
- Electrical Engineering
- Mechanical Engineering
- Data Science
WHAT YOU'LL BRING
- A passion for quality and continuous improvement.
- Curiosity and a data-driven mindset.
- The ability to collaborate effectively across multiple departments.
- A proactive approach to problem-solving and process improvements.
Ultradent is an Equal Opportunity Employer. We are a global culture where differences and perspectives are sought after, welcomed, and embraced. We consider all qualified applicants fairly, based on their experience, skills, and potential to contribute to our team. Our core values – Integrity, care, quality, innovation, and hard work – guide us daily. These values, when balanced, shape our workplace culture and ensure that we remain focused on our vision while maintaining a professional and inclusive environment.
VEVRAA Federal Contractor: For more information please contact us at Recruiting@ultradent.com
STEM OPT Medical Devices Job Roles in Utah
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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.