Medical Devices Green Card Sponsorship Jobs in Utah
Utah's medical devices sector is anchored by companies like Merit Medical Systems, Natus Medical, and BD (Becton Dickinson) operating across Salt Lake City, South Jordan, and Ogden. These employers regularly sponsor Green Cards for engineers, regulatory specialists, and quality professionals, making Utah one of the more active states for medical devices immigration sponsorship.
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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.
Green Card Medical Devices Job Roles in Utah
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Search Medical Devices Jobs in UtahMedical Devices Green Card Sponsorship Jobs in Utah: Frequently Asked Questions
Which medical devices companies sponsor Green Card visas in Utah?
Merit Medical Systems, headquartered in South Jordan, is one of Utah's largest medical devices employers and has a history of sponsoring Green Cards for skilled foreign nationals. BD (Becton Dickinson), Natus Medical, and various contract manufacturers along the Wasatch Front have also filed Green Card petitions. Sponsorship availability depends on the role, the employer's immigration policy, and current business needs.
Which cities in Utah have the most medical devices Green Card sponsorship jobs?
Salt Lake City and its suburbs, particularly South Jordan and Sandy, concentrate the highest number of medical devices employers in the state. Ogden and Provo also have a meaningful presence, with manufacturers and R&D operations operating along the I-15 corridor. Most Green Card sponsorship activity follows this same geographic pattern, as it tracks where the largest employers and most specialized roles are located.
What types of medical devices roles typically qualify for Green Card sponsorship?
Roles requiring a bachelor's degree or higher in a specific technical field are most commonly sponsored. This includes regulatory affairs specialists, quality engineers, mechanical and electrical engineers focused on device design, software engineers building embedded or connected medical systems, and clinical or R&D scientists. Positions where a specialized degree is a genuine requirement, rather than a preference, are generally the strongest candidates for employer-sponsored Green Card petitions.
How do I find medical devices Green Card sponsorship jobs in Utah?
Migrate Mate is built specifically for international job seekers and filters medical devices jobs in Utah that include Green Card sponsorship. Rather than sorting through thousands of general postings, you can search directly for roles where employers have indicated willingness to sponsor. This is particularly useful in Utah's medical devices sector, where sponsorship availability varies significantly from one company to the next even within the same city or product category.
Are there any Utah-specific considerations for Green Card sponsorship in the medical devices industry?
Utah's medical devices industry is heavily concentrated around the Wasatch Front, which means most sponsoring employers are mid-size manufacturers rather than large multinationals. These companies sometimes have less established immigration infrastructure than major corporations, so it's worth confirming early in the hiring process whether a company has previously filed Green Card petitions. Roles tied to FDA-regulated product development or manufacturing tend to have clearer sponsorship precedents within this segment of the industry.
What is the prevailing wage for Green Card medical devices jobs in Utah?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.