Medical Devices TN Sponsorship Jobs in Tennessee
Tennessee's medical devices sector spans manufacturing hubs in Memphis and Nashville, with major employers like Medline, Smith+Nephew, and Symmetry Medical operating across the state. Canadian and Mexican professionals in engineering, regulatory affairs, and quality assurance can pursue TN visa sponsorship through qualifying specialty occupations, making Tennessee a strong destination for international medical devices talent.
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Get Access To All JobsWhy join Stryker?
Looking for a place that values your unique talents? Discover Stryker's award-winning culture.
We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific.
Job description
We are excited to be named one of the World’s Best Workplaces by Fortune Magazine! We are proud to offer you 12 paid holidays annually. For an overview of our benefits and time off, please follow this link to learn more: US Stryker employee benefits. Stryker is hiring a Staff Chemical Process Engineer. In this role, you will develop and modify chemical process formulations, methods, and controls to meet quality standards, while recommending and implementing improvements to documentation. They will also review product development requirements to ensure compatibility with processing methods and integrate equipment and material capabilities to meet target specifications, costs, and schedules. This is an onsite role in Arlington, TN.
What you will do:
- Provide engineering support and leadership for product and process introductions, ensuring that all activities are completed and documented in accordance with the Stryker product procedures
- Ensure quality of process and product as defined in the appropriate operation and material specifications
- Lead the specification, development and implementation of manufacturing equipment based on analysis of specifications, reliability and regulatory requirements
- Analyze equipment and processes to establish operating data and conduct experimental test and result analysis
- Lead and participate in process review meetings
- Evaluate process layouts in terms of supporting new process integration while ensuring best utilization of floor space ensuring optimum process flow
- Lead and participate in process failure mode and effect analysis (PFMEA), control plan, standard operating procedures (SOP) and production part approval process (PPAP) generation associated with product transfers and launches
- Conduct process validations and measurement systems analysis (MSA) studies for new products and new processes
- Review and approve validation documentation
- Drive and execute effective communication with all stakeholders to enable project success
- Be proficient with and mentor others in usage of industry standards, including design requirements and test strategies per applicable regulations
- Lead creation and refinement of engineering documentation
- Provide training for manufacturing team members
- Ensure adherence to good manufacturing practices (GMP) and safety procedures
What you need:
Required:
- B.S. in Chemical, Mechanical, Manufacturing Engineering or related technical discipline
- 4+ years of manufacturing engineering or automation experience
Preferred qualifications:
- M.S. in Chemical Engineering
- FDA-regulated manufacturing/industry environment experience
- Knowledge of chemical processes for surface treatment
- Demonstrated experience in the field of formulations mixing (industrial process engineering)
- Custom automation experience
- Demonstrated experience writing and executing validations (IQ, OQ, PV, etc.)
- Demonstrated experience owning and resolving quality non-conformances and CAPAs
Compensation
- Salary Range: $89,300 - $148,800 USD Annual
Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&D insurance, and short-term disability insurance. Stryker offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Depending on customer requirements employees and new hires in sales and field roles that require access to customer accounts as a function of the job may be required to obtain various vaccinations as an essential function of their role.
Why join Stryker?
Looking for a place that values your unique talents? Discover Stryker's award-winning culture.
We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific.
Job description
We are excited to be named one of the World’s Best Workplaces by Fortune Magazine! We are proud to offer you 12 paid holidays annually. For an overview of our benefits and time off, please follow this link to learn more: US Stryker employee benefits. Stryker is hiring a Staff Chemical Process Engineer. In this role, you will develop and modify chemical process formulations, methods, and controls to meet quality standards, while recommending and implementing improvements to documentation. They will also review product development requirements to ensure compatibility with processing methods and integrate equipment and material capabilities to meet target specifications, costs, and schedules. This is an onsite role in Arlington, TN.
What you will do:
- Provide engineering support and leadership for product and process introductions, ensuring that all activities are completed and documented in accordance with the Stryker product procedures
- Ensure quality of process and product as defined in the appropriate operation and material specifications
- Lead the specification, development and implementation of manufacturing equipment based on analysis of specifications, reliability and regulatory requirements
- Analyze equipment and processes to establish operating data and conduct experimental test and result analysis
- Lead and participate in process review meetings
- Evaluate process layouts in terms of supporting new process integration while ensuring best utilization of floor space ensuring optimum process flow
- Lead and participate in process failure mode and effect analysis (PFMEA), control plan, standard operating procedures (SOP) and production part approval process (PPAP) generation associated with product transfers and launches
- Conduct process validations and measurement systems analysis (MSA) studies for new products and new processes
- Review and approve validation documentation
- Drive and execute effective communication with all stakeholders to enable project success
- Be proficient with and mentor others in usage of industry standards, including design requirements and test strategies per applicable regulations
- Lead creation and refinement of engineering documentation
- Provide training for manufacturing team members
- Ensure adherence to good manufacturing practices (GMP) and safety procedures
What you need:
Required:
- B.S. in Chemical, Mechanical, Manufacturing Engineering or related technical discipline
- 4+ years of manufacturing engineering or automation experience
Preferred qualifications:
- M.S. in Chemical Engineering
- FDA-regulated manufacturing/industry environment experience
- Knowledge of chemical processes for surface treatment
- Demonstrated experience in the field of formulations mixing (industrial process engineering)
- Custom automation experience
- Demonstrated experience writing and executing validations (IQ, OQ, PV, etc.)
- Demonstrated experience owning and resolving quality non-conformances and CAPAs
Compensation
- Salary Range: $89,300 - $148,800 USD Annual
Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&D insurance, and short-term disability insurance. Stryker offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Depending on customer requirements employees and new hires in sales and field roles that require access to customer accounts as a function of the job may be required to obtain various vaccinations as an essential function of their role.
TN Medical Devices Job Roles in Tennessee
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Search Medical Devices Jobs in TennesseeMedical Devices TN Sponsorship Jobs in Tennessee: Frequently Asked Questions
Which medical devices companies sponsor TN visas in Tennessee?
Tennessee hosts several established medical devices employers with a history of sponsoring TN visas for Canadian and Mexican professionals. Companies like Smith+Nephew, which has significant operations in Memphis, along with contract manufacturers and device distributors in the Nashville and Knoxville corridors, regularly hire for roles that qualify under TN specialty occupation categories such as engineering and scientific positions.
Which cities in Tennessee have the most medical devices TN sponsorship jobs?
Memphis is the dominant medical devices hub in Tennessee, home to a concentration of orthopedic and surgical device companies. Nashville follows closely, supported by the broader healthcare industry anchored there. Knoxville and the Tri-Cities region also have manufacturing and quality operations for device companies. Candidates looking for TN-eligible roles are most likely to find openings in Memphis and Nashville.
What types of medical devices roles typically qualify for TN sponsorship?
Roles that commonly qualify for TN status in the medical devices industry include mechanical and biomedical engineers, manufacturing engineers, quality engineers, regulatory affairs specialists with a science or engineering background, and research scientists. The position must require a bachelor's degree or higher in a specific field directly related to the job. General management or sales roles without a technical degree requirement typically do not qualify.
How do I find medical devices TN sponsorship jobs in Tennessee?
Migrate Mate is the most direct way to find medical devices jobs in Tennessee where employers are open to TN visa sponsorship. The platform filters specifically for TN-eligible roles, so you are not sorting through listings from employers unfamiliar with the visa category. Searching by the medical devices industry tag within Tennessee surfaces relevant openings in cities like Memphis and Nashville where device company hiring is most active.
Are there any Tennessee-specific considerations for TN visa sponsorship in medical devices?
Tennessee does not impose state-level work authorization requirements beyond federal standards, so TN visa holders can work for qualifying employers without additional state permits. However, roles in medical devices often involve FDA-regulated environments, meaning employers may require specific degree credentials that must align precisely with TN occupation categories. Candidates should confirm that their job title and degree field match a recognized TN specialty occupation before accepting an offer.