Manufacturing Associate Visa Sponsorship Jobs in Utah
Utah's manufacturing sector spans medical devices, aerospace components, and semiconductor production, with major employers like Merit Medical Systems, Northrop Grumman, and Autoliv operating facilities across Salt Lake City, Ogden, and Provo. International candidates pursuing manufacturing associate roles in Utah will find a growing base of employers with established visa sponsorship programs, particularly in precision manufacturing and life sciences.
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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.
Manufacturing Associate Job Roles in Utah
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Search Manufacturing Associate Jobs in UtahManufacturing Associate Jobs in Utah: Frequently Asked Questions
Which companies sponsor visas for manufacturing associates in Utah?
Merit Medical Systems, Autoliv, Northrop Grumman, and L3Harris are among Utah manufacturers with established international hiring. Medical device companies concentrated along the Wasatch Front tend to sponsor H-1B visa and other work visas for associates with specialized technical backgrounds. Sponsorship availability varies by role complexity, with positions requiring specific engineering or quality control credentials receiving the most consideration.
Which visa types are most common for manufacturing associate roles in Utah?
H-1B is the most frequently used visa for manufacturing associates in Utah, particularly for roles tied to engineering, quality systems, or process development that require a relevant bachelor's degree. TN visas apply to Canadian and Mexican nationals in qualifying technical occupations. Candidates already holding OPT or STEM OPT through Utah universities sometimes transition into full H-1B sponsorship through their manufacturing employers.
Which cities in Utah have the most manufacturing associate sponsorship jobs?
Salt Lake City and its surrounding suburbs, including Murray, West Valley City, and Sandy, concentrate the largest share of Utah manufacturing employment. Ogden supports aerospace and defense manufacturing through Hill Air Force Base-adjacent contractors. Provo and the broader Utah County corridor host semiconductor and medical device operations, making it a secondary hub for internationally sponsored manufacturing associate positions.
How to find manufacturing associate visa sponsorship jobs in Utah?
Migrate Mate filters manufacturing associate jobs in Utah specifically by visa sponsorship, so you're not sorting through postings that won't support international candidates. The platform aggregates roles from Utah employers in medical devices, aerospace, and electronics manufacturing. Searching by city, such as Salt Lake City or Ogden, helps narrow results to regions with the highest concentration of active sponsoring manufacturers.
Are there state-specific considerations for manufacturing associate visa sponsorship in Utah?
Utah's right-to-work status and relatively low unionization rate in manufacturing mean employers have more flexibility in hiring structures, which can streamline sponsorship decisions. The University of Utah and Brigham Young University supply engineering and materials science graduates who sometimes convert student visa status to employer sponsorship. Utah's growing life sciences corridor also means Department of Labor prevailing wage requirements for manufacturing associates can vary meaningfully between medical device and general industrial employers.
What is the prevailing wage for sponsored manufacturing associate 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.