Medical Devices F-1 STEM OPT Sponsorship 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.
See All Medical Devices JobsOverview
Showing 5 of 8+ Medical Devices F-1 STEM OPT Sponsorship Jobs in Utah
Have you applied for this role?
Have you applied for this role?
Have you applied for this role?
Have you applied for this role?
Have you applied for this role?
See all Medical Devices F-1 STEM OPT Sponsorship Jobs in Utah
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Medical Devices F-1 STEM OPT Sponsorship Jobs in Utah.
Get Access To All JobsWe are the people who give possibilities purpose
BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.
Job Description
Summary
The R&D team is seeking an exceptionally talented and passionate individual to help us identify and implement innovative solutions to address current and future health care needs in the Vascular Access markets. Within BD Medication Delivery Solutions (MDS) Research & Development, the associate in this position will be part of the Salt Lake City R&D team. Our R&D Engineers are responsible for developing and implementing new product designs, product improvements, and critical component changes for disposable and durable medical devices. This position assists the R&D Engineering Teams in designing, developing, and implementing new products, processes, test methods and equipment. This position is also responsible for system development and improvement, along with managing projects with divisional impact.
The preferred candidate will have strong technical design skills with excellent technical judgment, professional written and oral skills, and team-oriented with great leadership abilities. This candidate should possess a strong ability to interpret and ensure compliance with all local, state, federal and BD safety regulations, quality policies, best practices, and procedures through appropriate communication. Having a diverse technical background along with strong interpersonal skills will be key for success in this role.
Job Responsibilities (Primary Duties, Roles, and/or Authorities)
- Consultant/Division expert; Division Technical expert.
- Develops innovative ideas for the organization.
- Broad business and technical understanding.
- Influences and directs others across the organization; coaches/mentors.
- Critical decision maker in areas of engineering and business needs.
- Leads new product development projects.
- Initiates new or revised documentation and tracks through appropriate approval cycles and implementation.
- Participates in and leads cross-functional teams and/or projects.
- Provides technical support on components, material methods, systems, processes, and/or equipment.
- Develops physical and functional test requirements to assure specifications and regulations are met.
- Writes and approves protocols, reports, and data.
- Manages testing outlined in protocols and test methods.
- Manages and develops validation studies on equipment and processes.
- Conducts and/or supports product complaint investigations.
- Understands and follows company procedures and regulatory requirements.
- Participates in and provides input to training on department and division procedures and policies.
- Manages project planning, budgeting, scheduling, and tracking.
- Analyzes problems in design, process, and/or test development; recommends and implements solutions.
- Prepares and presents oral and written project updates and technical discussions.
- Develops and implements procedures and policies.
- Develops and implements manufacturing procedures.
The duties and responsibilities are intended to be representative of the work performed by the incumbent(s) in this position and are not all-inclusive. The omission of a specific duty or responsibility will not preclude it from the position.
Minimum Requirements:
- Bachelor’s degree in STEM (Science, Technology, Engineering, Math)
- 6 years of engineering experience within the medical device or equivalent regulated industry.
- Experience having ownership of making and present engineering decisions.
- Experience managing multiple projects from initiation through closing phases (Determine and communicate project deliverables, develop a work breakdown structure and estimates, develop a viable schedule and management plans, Execute and control the project through closure).
- Experience training (creating, and critiquing training).
- Experience applying comparative statistics, as required.
- Extensive Software application skills.
- Experience creating, reviewing, and coordinating test protocols and reports.
- Experience generating engineering proposals.
Preferred Knowledge and Qualification Skills:
- Master's degree in STEM with at least 4 years of engineering experience within the medical device or equivalent regulated industry.
- Experience with specific specialized engineering skills (Creating engineering cost analysis. Basic tooling design and drafting knowledge, Analyze and optimize existing processes and create new processes. Create, analyze, and optimize relevant manufacturing and quality systems).
- Deep Knowledge in Material Science.
- Well versed in Bioengineering principles.
- Understanding of disciplined product development processes and quality requirements.
- Understanding and ability to design for high-volume manufacturing and/or durable electro/mechanical medical devices.
- Experience with specific tools and methods, such as statistical tools and Design of Experiments (DOE), computer analysis, and engineering fundamentals to support sound engineering judgment.
- SolidWorks, Minitab, and FEA (Abaqus/Fluent) experience.
- Knowledge of regulatory and quality requirements (21 CFR 820.30).
- Understanding of failure theory and modes for plastics, elastomers, and metals due to static and time-variable loading conditions.
- Experience with clinical studies, human physiology, and simulated product use studies.
- Experience with contact and non-contact metrology.
- Knowledge of high-volume manufacturing and assembly processes, particularly those of plastic injection molding, metal stamping, and automated assembly techniques, including solvent bonding, adhesive bonding, ultrasonic welding, and interference-fitting.
- Experience with manufacturing process validation, including strategy development, First Article Inspection, and Factory Acceptance Testing.
- Comprehensive understanding of the regulatory environment.
- Experience creating and controlling a budget.
- Strong fit with BD values.
Physical Demands
This position is in an office and laboratory environment and requires the incumbent to sit, stand and perform general office functions. The incumbent may also be required to lift up to twenty-five pounds occasionally. The incumbent may be required to stand for extended periods. Bending, stooping, and reaching are also frequently required.
At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.
For certain roles at BD, employment is contingent upon the Company’s receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD’s Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.
Why Join Us?
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you’ll discover a culture in which you can learn, grow and thrive.
We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.
Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.
Required Skills
New Product Development, Product Design, Product Development, Product Development Projects
Optional Skills
Design of Experiments (DOE), Medical Device Industry, Medical Devices, Regulated Industries
Primary Work Location
USA UT - Sandy
Additional Locations
USA UT - Salt Lake City
Work Shift
We are the people who give possibilities purpose
BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.
Job Description
Summary
The R&D team is seeking an exceptionally talented and passionate individual to help us identify and implement innovative solutions to address current and future health care needs in the Vascular Access markets. Within BD Medication Delivery Solutions (MDS) Research & Development, the associate in this position will be part of the Salt Lake City R&D team. Our R&D Engineers are responsible for developing and implementing new product designs, product improvements, and critical component changes for disposable and durable medical devices. This position assists the R&D Engineering Teams in designing, developing, and implementing new products, processes, test methods and equipment. This position is also responsible for system development and improvement, along with managing projects with divisional impact.
The preferred candidate will have strong technical design skills with excellent technical judgment, professional written and oral skills, and team-oriented with great leadership abilities. This candidate should possess a strong ability to interpret and ensure compliance with all local, state, federal and BD safety regulations, quality policies, best practices, and procedures through appropriate communication. Having a diverse technical background along with strong interpersonal skills will be key for success in this role.
Job Responsibilities (Primary Duties, Roles, and/or Authorities)
- Consultant/Division expert; Division Technical expert.
- Develops innovative ideas for the organization.
- Broad business and technical understanding.
- Influences and directs others across the organization; coaches/mentors.
- Critical decision maker in areas of engineering and business needs.
- Leads new product development projects.
- Initiates new or revised documentation and tracks through appropriate approval cycles and implementation.
- Participates in and leads cross-functional teams and/or projects.
- Provides technical support on components, material methods, systems, processes, and/or equipment.
- Develops physical and functional test requirements to assure specifications and regulations are met.
- Writes and approves protocols, reports, and data.
- Manages testing outlined in protocols and test methods.
- Manages and develops validation studies on equipment and processes.
- Conducts and/or supports product complaint investigations.
- Understands and follows company procedures and regulatory requirements.
- Participates in and provides input to training on department and division procedures and policies.
- Manages project planning, budgeting, scheduling, and tracking.
- Analyzes problems in design, process, and/or test development; recommends and implements solutions.
- Prepares and presents oral and written project updates and technical discussions.
- Develops and implements procedures and policies.
- Develops and implements manufacturing procedures.
The duties and responsibilities are intended to be representative of the work performed by the incumbent(s) in this position and are not all-inclusive. The omission of a specific duty or responsibility will not preclude it from the position.
Minimum Requirements:
- Bachelor’s degree in STEM (Science, Technology, Engineering, Math)
- 6 years of engineering experience within the medical device or equivalent regulated industry.
- Experience having ownership of making and present engineering decisions.
- Experience managing multiple projects from initiation through closing phases (Determine and communicate project deliverables, develop a work breakdown structure and estimates, develop a viable schedule and management plans, Execute and control the project through closure).
- Experience training (creating, and critiquing training).
- Experience applying comparative statistics, as required.
- Extensive Software application skills.
- Experience creating, reviewing, and coordinating test protocols and reports.
- Experience generating engineering proposals.
Preferred Knowledge and Qualification Skills:
- Master's degree in STEM with at least 4 years of engineering experience within the medical device or equivalent regulated industry.
- Experience with specific specialized engineering skills (Creating engineering cost analysis. Basic tooling design and drafting knowledge, Analyze and optimize existing processes and create new processes. Create, analyze, and optimize relevant manufacturing and quality systems).
- Deep Knowledge in Material Science.
- Well versed in Bioengineering principles.
- Understanding of disciplined product development processes and quality requirements.
- Understanding and ability to design for high-volume manufacturing and/or durable electro/mechanical medical devices.
- Experience with specific tools and methods, such as statistical tools and Design of Experiments (DOE), computer analysis, and engineering fundamentals to support sound engineering judgment.
- SolidWorks, Minitab, and FEA (Abaqus/Fluent) experience.
- Knowledge of regulatory and quality requirements (21 CFR 820.30).
- Understanding of failure theory and modes for plastics, elastomers, and metals due to static and time-variable loading conditions.
- Experience with clinical studies, human physiology, and simulated product use studies.
- Experience with contact and non-contact metrology.
- Knowledge of high-volume manufacturing and assembly processes, particularly those of plastic injection molding, metal stamping, and automated assembly techniques, including solvent bonding, adhesive bonding, ultrasonic welding, and interference-fitting.
- Experience with manufacturing process validation, including strategy development, First Article Inspection, and Factory Acceptance Testing.
- Comprehensive understanding of the regulatory environment.
- Experience creating and controlling a budget.
- Strong fit with BD values.
Physical Demands
This position is in an office and laboratory environment and requires the incumbent to sit, stand and perform general office functions. The incumbent may also be required to lift up to twenty-five pounds occasionally. The incumbent may be required to stand for extended periods. Bending, stooping, and reaching are also frequently required.
At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.
For certain roles at BD, employment is contingent upon the Company’s receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD’s Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.
Why Join Us?
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you’ll discover a culture in which you can learn, grow and thrive.
We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.
Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.
Required Skills
New Product Development, Product Design, Product Development, Product Development Projects
Optional Skills
Design of Experiments (DOE), Medical Device Industry, Medical Devices, Regulated Industries
Primary Work Location
USA UT - Sandy
Additional Locations
USA UT - Salt Lake City
Work Shift
Medical Devices Job Roles in Utah
See all Medical Devices 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 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.