Medical Devices H-1B Sponsorship Jobs in Tennessee
Tennessee's medical devices sector spans Nashville, Memphis, and the greater Knoxville area, with major employers like Medtronic, Smith+Nephew, and Symmetry Medical regularly filing H-1B visa petitions for engineers, regulatory specialists, and R&D professionals. The state's manufacturing base and proximity to Vanderbilt and UT research institutions make it a genuine hub for international talent seeking H-1B sponsorship in medical devices.
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Get Access To All JobsWe anticipate the application window for this opening will close on - 7 Nov 2026
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.
A Day in the Life
The Cranial and Spinal Technologies (CST) Operating Unit develops and delivers technologies for treating spinal and cranial conditions. The organization partners with healthcare professionals worldwide to support procedural planning, navigation, biologics, implants, and enabling technologies designed to improve patient outcomes.
The Regulatory Affairs function supports product compliance and regulatory strategy throughout the product lifecycle by coordinating submissions, registrations, renewals, and regulatory documentation. This team collaborates with cross-functional stakeholders to help ensure products, processes, and labeling activities meet applicable regulatory requirements while supporting business objectives within the CST portfolio.
This position is based in Memphis, Tennessee, and is an on-site role. No travel is required.
Job Description field
The Associate Regulatory Affairs Specialist supports regulatory activities for the Cranial and Spinal Technologies portfolio by coordinating documentation, preparing submission materials, maintaining regulatory records, and assisting with compliance initiatives. This role partners with cross-functional teams to help ensure timely and accurate regulatory submissions while supporting regulatory inspections, audits, and ongoing business operations.
Primary Responsibilities
- Coordinate the preparation, assembly, and maintenance of regulatory submission packages and supporting documentation.
- Compile materials required for regulatory submissions, license renewals, annual registrations, and related filings.
- Support internal and external audits, inspections, and regulatory inquiries by gathering and organizing requested documentation.
- Review regulatory documentation and recommend updates to labeling, manufacturing processes, marketing materials, and clinical protocols to support compliance requirements.
- Maintain and improve systems used to track regulatory submissions, commitments, approvals, and records.
- Monitor regulatory requirements, guidance updates, and procedural changes to support ongoing compliance activities.
- Collaborate with cross-functional teams to ensure regulatory deliverables are completed accurately and according to established timelines.
- Support regulatory strategies and activities associated with obtaining and maintaining product approvals and registrations.
Required Qualifications
Bachelor's degree
Preferred Qualifications
- Experience supporting regulatory submissions, registrations, renewals, or regulatory compliance activities.
- 1+ year of experience in Regulatory Affairs, Quality, Clinical, Medical Device, Life Sciences, Healthcare, or another regulated environment.
- Knowledge of United States and/or international regulatory requirements and regulatory documentation practices.
- Experience using Microsoft Office applications, including Word, Excel, Outlook, and PowerPoint.
- Experience using regulatory information management, document control, or quality management systems.
For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required.
Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.
U.S. Work Authorization & Sponsorship
At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.
Recruitment Fraud Alert
We are aware of phishing scams targeting job seekers. Please keep the following in mind:
Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.
Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.
If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.
If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com.
Benefits & Compensation
Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
Salary ranges for U.S (excl. PR) locations (USD): $60,800.00 - $91,200.00
The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others). The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).
The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).
Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.
Further details are available at the link below:
Medtronic benefits and compensation plans
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
If you are applying to perform work for Medtronic, Inc. (“Medtronic”) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
We anticipate the application window for this opening will close on - 7 Nov 2026
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.
A Day in the Life
The Cranial and Spinal Technologies (CST) Operating Unit develops and delivers technologies for treating spinal and cranial conditions. The organization partners with healthcare professionals worldwide to support procedural planning, navigation, biologics, implants, and enabling technologies designed to improve patient outcomes.
The Regulatory Affairs function supports product compliance and regulatory strategy throughout the product lifecycle by coordinating submissions, registrations, renewals, and regulatory documentation. This team collaborates with cross-functional stakeholders to help ensure products, processes, and labeling activities meet applicable regulatory requirements while supporting business objectives within the CST portfolio.
This position is based in Memphis, Tennessee, and is an on-site role. No travel is required.
Job Description field
The Associate Regulatory Affairs Specialist supports regulatory activities for the Cranial and Spinal Technologies portfolio by coordinating documentation, preparing submission materials, maintaining regulatory records, and assisting with compliance initiatives. This role partners with cross-functional teams to help ensure timely and accurate regulatory submissions while supporting regulatory inspections, audits, and ongoing business operations.
Primary Responsibilities
- Coordinate the preparation, assembly, and maintenance of regulatory submission packages and supporting documentation.
- Compile materials required for regulatory submissions, license renewals, annual registrations, and related filings.
- Support internal and external audits, inspections, and regulatory inquiries by gathering and organizing requested documentation.
- Review regulatory documentation and recommend updates to labeling, manufacturing processes, marketing materials, and clinical protocols to support compliance requirements.
- Maintain and improve systems used to track regulatory submissions, commitments, approvals, and records.
- Monitor regulatory requirements, guidance updates, and procedural changes to support ongoing compliance activities.
- Collaborate with cross-functional teams to ensure regulatory deliverables are completed accurately and according to established timelines.
- Support regulatory strategies and activities associated with obtaining and maintaining product approvals and registrations.
Required Qualifications
Bachelor's degree
Preferred Qualifications
- Experience supporting regulatory submissions, registrations, renewals, or regulatory compliance activities.
- 1+ year of experience in Regulatory Affairs, Quality, Clinical, Medical Device, Life Sciences, Healthcare, or another regulated environment.
- Knowledge of United States and/or international regulatory requirements and regulatory documentation practices.
- Experience using Microsoft Office applications, including Word, Excel, Outlook, and PowerPoint.
- Experience using regulatory information management, document control, or quality management systems.
For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required.
Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.
U.S. Work Authorization & Sponsorship
At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.
Recruitment Fraud Alert
We are aware of phishing scams targeting job seekers. Please keep the following in mind:
Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.
Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.
If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.
If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com.
Benefits & Compensation
Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
Salary ranges for U.S (excl. PR) locations (USD): $60,800.00 - $91,200.00
The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others). The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).
The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).
Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.
Further details are available at the link below:
Medtronic benefits and compensation plans
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
If you are applying to perform work for Medtronic, Inc. (“Medtronic”) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
H-1B Medical Devices Job Roles in Tennessee
See all 117+ Medical Devices H-1B Jobs in Tennessee
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Search Medical Devices Jobs in TennesseeMedical Devices H-1B Sponsorship Jobs in Tennessee: Frequently Asked Questions
Which medical devices companies sponsor H-1B visas in Tennessee?
Medtronic has a significant manufacturing and engineering presence in Tennessee and has historically filed H-1B visa petitions. Smith+Nephew operates facilities in Memphis. Other active filers in the state's medical devices space include Symmetry Medical and smaller contract manufacturers concentrated around Nashville and the I-40 corridor. Filing history varies year to year, so checking DOL LCA disclosure data for specific employers is the most reliable approach.
Which cities in Tennessee have the most medical devices H-1B sponsorship jobs?
Nashville is Tennessee's primary hub for medical devices H-1B roles, driven by its concentration of healthcare corporations and device manufacturers. Memphis is a secondary center, particularly for manufacturing and supply chain positions tied to orthopedic and surgical device companies. Knoxville sees activity connected to University of Tennessee research partnerships and regional manufacturers, though at lower volume than Nashville or Memphis.
What types of medical devices roles typically qualify for H-1B sponsorship?
Roles that qualify for H-1B sponsorship must meet the specialty occupation standard, requiring at least a bachelor's degree in a specific field directly related to the position. In medical devices, this commonly covers quality engineers, regulatory affairs specialists, biomedical engineers, R&D scientists, manufacturing process engineers, and software engineers working on device software or embedded systems. General production or assembly roles typically do not meet the specialty occupation threshold.
How do I find medical devices H-1B sponsorship jobs in Tennessee?
Migrate Mate is built specifically for international job seekers and filters medical devices H-1B sponsorship jobs in Tennessee by employer, role type, and visa category. Because sponsorship willingness varies significantly by company and hiring cycle, having a focused search tool matters. Migrate Mate surfaces roles from employers with documented H-1B filing history, reducing time spent on applications where sponsorship is unlikely.
Are there state-specific considerations for H-1B sponsorship in Tennessee's medical devices industry?
Tennessee has no state income tax on wages, which affects total compensation structuring but does not change federal H-1B requirements. Employers must still file a Labor Condition Application with the DOL certifying that the offered wage meets the prevailing wage for the role and location. Medical devices roles in Tennessee often fall under FDA-regulated environments, so regulatory affairs and quality positions may require additional credentials that employers factor into their hiring and sponsorship decisions.
What is the prevailing wage for H-1B medical devices jobs in Tennessee?
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.