Medical Devices F-1 STEM OPT Sponsorship Jobs in Tennessee
Medical devices F-1 STEM OPT sponsorship jobs in Tennessee are concentrated in Nashville, Memphis, and Knoxville, where companies like Medline Industries, Smith+Nephew, and Vanderbilt University Medical Center hire biomedical engineers, quality engineers, and regulatory affairs specialists. Tennessee's strong manufacturing base and research hospital network make it an active state for STEM OPT candidates in medical devices.
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Get Access To All JobsINTRODUCTION
Life Unlimited. At Smith+Nephew, we design and manufacture technology that takes the limits off living. As a Quality Engineer, you’ll play a critical role in ensuring our product integrity and driving continuous improvement in a fast-paced, production environment. This position offers the opportunity to apply your technical expertise to campus-wide digitization initiatives as we transition our business to Industry 4.0/5.0. Prospective candidates must have an eagerness to learn, foundational understanding of cGMP, strong communication skills, and keen attention to detail.
ROLE AND RESPONSIBILITIES
- The Quality Engineer will report to the Operations Quality Engineering Team. This role works cross-functionally with other departments to support daily production targets, transformational projects, and continuous improvement initiatives. This role is responsible for maintaining compliance to internal and external standards and regulations, both within the QMS and on the production floor.
-
Coordinates and leads countermeasure meetings to review processes, perform gap analyses, and implement new technologies.
-
Works with cross-functional teams in the resolution of quality problems, which may involve processing of NCRs, CAPAs, material dispositions, data trending and analysis, and presentation to internal customers and external vendors.
-
Develops, documents, and implements various inspection techniques and procedures to ensure product integrity to design specifications.
-
Coordinates with other Engineers and Metrology personnel on the review, design, development, and procurement of product gauging.
-
Coordinates development and implementation of digitized processes, which may include writing work instructions, app development, and case testing.
-
Trains Manufacturing and Quality Control associates on business processes and inspection techniques.
-
Works with Manufacturing Engineers to perform first article inspections, capability studies, validations (IQ, OQ, PQ), and engineering analyses to characterize products, processes, and materials.
-
Coordinates with Design Quality and Product Development on new product introductions, including the evaluation of critical features and proposed inspection techniques.
BASIC QUALIFICATIONS
- Education: Bachelor of Science in Mechanical, Manufacturing, Electrical, Biomedical, Industrial Engineering, or equivalent technical discipline required.
-
Licenses/Certifications: ASQ CQE and Six Sigma Green or Black Belt preferred.
-
Experience: 0-3 years in a quality, engineering, or manufacturing role preferred.
-
Foundational understanding of cGMP and quality systems in a regulated industry.
-
Strong analytical and problem solving skills with experience in data analysis and root cause methodologies.
-
Ability to read and interpret technical drawings, specifications, and GD&T.
-
Clear written and verbal communication skills with the ability to present to cross functional audiences.
-
Experience with statistical tools, software development, or digital manufacturing platforms preferred.
-
Familiarity with Tulip, Jira, and Agile methodologies preferred.
-
Ability to stand or sit for extended periods and perform hands on measurement using basic inspection tools.
Physical Requirements
- Ability to measure product using simple hand instruments, stand, or sit for extended periods.
- Vision must be excellent or corrected.
TRAVEL
- 0-10%
PREFERRED QUALIFICATIONS
- You. Unlimited. We believe in creating the greatest good for society. Our strongest investments are in our people and the patients we serve.
-
Inclusion and Belonging- Committed to Welcoming, Celebrating and Thriving on Inclusion and Belonging, Learn more about Employee Inclusion Groups on our website.
-
Your Future: 401k Matching Program, 401k Plus Program, Discounted Stock Purchase Plan, Tuition Reimbursement.
-
Work/Life Balance: Flexible Personal and Vacation Time Off, Paid Holidays, Flex Holidays, Paid Community Service Day.
-
Your Wellbeing: Medical, Dental, Vision, Health Savings Account with Employer Contribution, Employee Assistance Program, Parental Leave, Fertility and Adoption Assistance Program.
-
Flexibility: Hybrid Work Model for most professional roles.
-
Training: Hands On, Team Customized, Mentorship.
-
Extra Perks: Discounts on fitness clubs, travel and more.
Smith+Nephew provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability.
INTRODUCTION
Life Unlimited. At Smith+Nephew, we design and manufacture technology that takes the limits off living. As a Quality Engineer, you’ll play a critical role in ensuring our product integrity and driving continuous improvement in a fast-paced, production environment. This position offers the opportunity to apply your technical expertise to campus-wide digitization initiatives as we transition our business to Industry 4.0/5.0. Prospective candidates must have an eagerness to learn, foundational understanding of cGMP, strong communication skills, and keen attention to detail.
ROLE AND RESPONSIBILITIES
- The Quality Engineer will report to the Operations Quality Engineering Team. This role works cross-functionally with other departments to support daily production targets, transformational projects, and continuous improvement initiatives. This role is responsible for maintaining compliance to internal and external standards and regulations, both within the QMS and on the production floor.
-
Coordinates and leads countermeasure meetings to review processes, perform gap analyses, and implement new technologies.
-
Works with cross-functional teams in the resolution of quality problems, which may involve processing of NCRs, CAPAs, material dispositions, data trending and analysis, and presentation to internal customers and external vendors.
-
Develops, documents, and implements various inspection techniques and procedures to ensure product integrity to design specifications.
-
Coordinates with other Engineers and Metrology personnel on the review, design, development, and procurement of product gauging.
-
Coordinates development and implementation of digitized processes, which may include writing work instructions, app development, and case testing.
-
Trains Manufacturing and Quality Control associates on business processes and inspection techniques.
-
Works with Manufacturing Engineers to perform first article inspections, capability studies, validations (IQ, OQ, PQ), and engineering analyses to characterize products, processes, and materials.
-
Coordinates with Design Quality and Product Development on new product introductions, including the evaluation of critical features and proposed inspection techniques.
BASIC QUALIFICATIONS
- Education: Bachelor of Science in Mechanical, Manufacturing, Electrical, Biomedical, Industrial Engineering, or equivalent technical discipline required.
-
Licenses/Certifications: ASQ CQE and Six Sigma Green or Black Belt preferred.
-
Experience: 0-3 years in a quality, engineering, or manufacturing role preferred.
-
Foundational understanding of cGMP and quality systems in a regulated industry.
-
Strong analytical and problem solving skills with experience in data analysis and root cause methodologies.
-
Ability to read and interpret technical drawings, specifications, and GD&T.
-
Clear written and verbal communication skills with the ability to present to cross functional audiences.
-
Experience with statistical tools, software development, or digital manufacturing platforms preferred.
-
Familiarity with Tulip, Jira, and Agile methodologies preferred.
-
Ability to stand or sit for extended periods and perform hands on measurement using basic inspection tools.
Physical Requirements
- Ability to measure product using simple hand instruments, stand, or sit for extended periods.
- Vision must be excellent or corrected.
TRAVEL
- 0-10%
PREFERRED QUALIFICATIONS
- You. Unlimited. We believe in creating the greatest good for society. Our strongest investments are in our people and the patients we serve.
-
Inclusion and Belonging- Committed to Welcoming, Celebrating and Thriving on Inclusion and Belonging, Learn more about Employee Inclusion Groups on our website.
-
Your Future: 401k Matching Program, 401k Plus Program, Discounted Stock Purchase Plan, Tuition Reimbursement.
-
Work/Life Balance: Flexible Personal and Vacation Time Off, Paid Holidays, Flex Holidays, Paid Community Service Day.
-
Your Wellbeing: Medical, Dental, Vision, Health Savings Account with Employer Contribution, Employee Assistance Program, Parental Leave, Fertility and Adoption Assistance Program.
-
Flexibility: Hybrid Work Model for most professional roles.
-
Training: Hands On, Team Customized, Mentorship.
-
Extra Perks: Discounts on fitness clubs, travel and more.
Smith+Nephew provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability.
Medical Devices Job Roles in Tennessee
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Search Medical Devices Jobs in TennesseeMedical Devices Jobs in Tennessee: Frequently Asked Questions
Which medical devices companies sponsor F-1 STEM OPT visas in Tennessee?
Tennessee-based medical devices employers with documented STEM OPT hiring include Smith+Nephew in Memphis, which has a significant orthopedic manufacturing presence, Medline Industries, and device divisions affiliated with Vanderbilt University Medical Center in Nashville. Larger contract manufacturers and original equipment manufacturers in the state have also filed Labor Condition Applications for engineering and quality roles, which indicates a pattern of sponsoring international candidates.
Which cities in Tennessee have the most medical devices F-1 STEM OPT sponsorship jobs?
Nashville leads Tennessee for medical devices STEM OPT opportunities, driven by its hospital network and affiliated device suppliers. Memphis is a secondary hub anchored by orthopedic and surgical device companies, particularly around the medical corridor near the medical district. Knoxville and the Oak Ridge corridor attract candidates in biomedical instrumentation and materials science roles connected to research institutions and advanced manufacturing facilities in East Tennessee.
What types of medical devices roles typically qualify for F-1 STEM OPT sponsorship?
Roles that commonly qualify have a direct connection to a STEM degree. In Tennessee's medical devices sector, these include biomedical engineering, quality engineering, regulatory affairs, manufacturing process engineering, R&D engineering, and software development for embedded medical systems. The role must appear on an employer's E-Verify enrollment, the employer must sign a training plan through your DSO, and the position must align with your degree field for STEM OPT extension eligibility.
How do I find medical devices F-1 STEM OPT sponsorship jobs in Tennessee?
Migrate Mate filters job listings specifically by visa type and state, so you can search for medical devices F-1 STEM OPT roles in Tennessee without manually screening hundreds of postings. Because Migrate Mate surfaces DOL Labor Condition Application filing history, you can identify which Tennessee employers have actually sponsored international candidates in device engineering and quality roles, rather than relying on unverified claims in job descriptions.
Are there any Tennessee-specific considerations for F-1 STEM OPT sponsorship in medical devices?
Tennessee does not impose additional state-level work authorization requirements beyond federal STEM OPT rules, but medical devices roles in the state often involve FDA-regulated manufacturing environments where background checks and drug screenings are standard. Employers in Tennessee's device sector who hold FDA facility registrations are generally familiar with international hiring compliance. Confirming that a prospective employer is enrolled in E-Verify before accepting an offer is essential for STEM OPT extension eligibility.