Medical Devices TN Sponsorship Jobs in Texas
Texas is one of the strongest states for medical devices TN visa sponsorship jobs, anchored by major employers like Medtronic, Abbott, and Becton Dickinson across the Dallas-Fort Worth metroplex, Austin, and Houston. Canadian and Mexican professionals in engineering, science, and technical roles will find a dense concentration of device manufacturers, contract research organizations, and regional headquarters actively hiring.
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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.
Sr. Staff Design Quality Engineer – Flower Mound, Texas
You’ll partner with product development teams to deliver design quality for complex electromechanical medical devices and consumables. This role focuses on translating user needs into design requirements, guiding risk and test strategies, and ensuring design documentation and verification align with global medical device standards. You lead technical problem solving, mentor others, and collaborate across functions to advance products through design, development, and launch.
You will support the Urology portfolio, including legacy products and a recently launched product integrating capital equipment, visualization platforms, and fluid management technologies.
What you will do
- Lead design quality activities for electrical components, subsystems, and system-level designs on complex electromechanical medical devices and consumables.
- Support products in the midst of launch and post-market stabilization, navigating evolving priorities while maintaining design control rigor and risk-based decision making.
- Translate user needs into design inputs/specifications and maintain traceability through design outputs, verification, and validation deliverables.
- Define and execute advanced prototyping, test methods, and verification strategies aligned to applicable standards (e.g., IEC 60601, IEC 62304) and project plans.
- Identify and resolve complex product design issues by driving root cause investigations, design tradeoff decisions, and design changes with documented rationale.
- Create and refine regulated design documentation (including Design History File content) and mentor teams on good documentation practices and required technical evidence.
- Apply and coach risk management, corrective and preventive action, audit readiness, and statistical methods within design and development activities.
- Partner with cross-functional stakeholders (Quality, Manufacturing, Regulatory, Clinical, Marketing, and Project Management) to plan and deliver design reviews, milestones, and release readiness.
- Support direct customer and surgeon engagement, including voice-of-customer activities, field feedback, and quality events or complaints tied to design or usability, translating real-world use into design improvements.
What you will need
Required
- Bachelor’s degree in Science, Engineering, or a related discipline.
- Minimum 6 years of experience in medical device product development and/or design quality engineering.
- Experience working within highly regulated industries with formal quality systems and design documentation practices (e.g., ISO 13485 or comparable industry standards).
- Experience with design controls, risk management, and verification/validation planning for electro-mechanical products.
Preferred
- A master’s degree in a relevant discipline and certifications such as Certified Quality Engineer (CQE), Certified Reliability Engineer (CRE), or Six Sigma Green or Black Belt.
- Experience supporting new product launches and post-market design improvements for complex electromechanical medical devices and consumables.
- Experience with medical device design and software lifecycle standards (e.g., IEC 60601, IEC 62304).
-
Hands-on experience evaluating and testing:
-
Software code (C, C++, C#)
- Electronic designs, including printed circuit board assemblies and subsystems
- Mechanical designs and technical drawings
US10: $129,800 - $216,400 USD Annual
View the U.S. work location and transparency guide to find the pay range for your location.
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.
Sr. Staff Design Quality Engineer – Flower Mound, Texas
You’ll partner with product development teams to deliver design quality for complex electromechanical medical devices and consumables. This role focuses on translating user needs into design requirements, guiding risk and test strategies, and ensuring design documentation and verification align with global medical device standards. You lead technical problem solving, mentor others, and collaborate across functions to advance products through design, development, and launch.
You will support the Urology portfolio, including legacy products and a recently launched product integrating capital equipment, visualization platforms, and fluid management technologies.
What you will do
- Lead design quality activities for electrical components, subsystems, and system-level designs on complex electromechanical medical devices and consumables.
- Support products in the midst of launch and post-market stabilization, navigating evolving priorities while maintaining design control rigor and risk-based decision making.
- Translate user needs into design inputs/specifications and maintain traceability through design outputs, verification, and validation deliverables.
- Define and execute advanced prototyping, test methods, and verification strategies aligned to applicable standards (e.g., IEC 60601, IEC 62304) and project plans.
- Identify and resolve complex product design issues by driving root cause investigations, design tradeoff decisions, and design changes with documented rationale.
- Create and refine regulated design documentation (including Design History File content) and mentor teams on good documentation practices and required technical evidence.
- Apply and coach risk management, corrective and preventive action, audit readiness, and statistical methods within design and development activities.
- Partner with cross-functional stakeholders (Quality, Manufacturing, Regulatory, Clinical, Marketing, and Project Management) to plan and deliver design reviews, milestones, and release readiness.
- Support direct customer and surgeon engagement, including voice-of-customer activities, field feedback, and quality events or complaints tied to design or usability, translating real-world use into design improvements.
What you will need
Required
- Bachelor’s degree in Science, Engineering, or a related discipline.
- Minimum 6 years of experience in medical device product development and/or design quality engineering.
- Experience working within highly regulated industries with formal quality systems and design documentation practices (e.g., ISO 13485 or comparable industry standards).
- Experience with design controls, risk management, and verification/validation planning for electro-mechanical products.
Preferred
- A master’s degree in a relevant discipline and certifications such as Certified Quality Engineer (CQE), Certified Reliability Engineer (CRE), or Six Sigma Green or Black Belt.
- Experience supporting new product launches and post-market design improvements for complex electromechanical medical devices and consumables.
- Experience with medical device design and software lifecycle standards (e.g., IEC 60601, IEC 62304).
-
Hands-on experience evaluating and testing:
-
Software code (C, C++, C#)
- Electronic designs, including printed circuit board assemblies and subsystems
- Mechanical designs and technical drawings
US10: $129,800 - $216,400 USD Annual
View the U.S. work location and transparency guide to find the pay range for your location.
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 Texas
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Search Medical Devices Jobs in TexasMedical Devices TN Sponsorship Jobs in Texas: Frequently Asked Questions
Which medical devices companies sponsor TN visas in Texas?
Texas hosts several large medical devices employers with established TN visa sponsorship track records, including Medtronic, Abbott Laboratories, Becton Dickinson, and Stryker, which maintain significant operations in the Dallas-Fort Worth area and Austin. Smaller contract manufacturers and medical technology firms in the Texas Medical Center in Houston also hire TN workers, particularly for engineering and scientific roles. Sponsorship practices vary by company and hiring team.
Which cities in Texas have the most medical devices TN sponsorship jobs?
Dallas-Fort Worth is the leading hub, home to regional headquarters and manufacturing sites for several global device companies. Austin has grown substantially as a medical technology and health tech center, attracting engineering-focused employers. Houston's Texas Medical Center, the largest medical complex in the world, supports a range of device and diagnostics companies. San Antonio also has a smaller but active cluster of medical device and healthcare technology employers.
What types of medical devices roles typically qualify for TN sponsorship?
TN visa eligibility requires that the role falls within an approved USMCA occupation category and that the applicant holds a qualifying degree. In medical devices, roles that commonly meet this standard include biomedical engineers, electrical and mechanical engineers working on device development, quality assurance scientists, regulatory affairs professionals with scientific backgrounds, and clinical research associates. Purely sales or administrative positions generally do not qualify unless they have a clear scientific or engineering component.
How do I find medical devices TN sponsorship jobs in Texas?
Migrate Mate is built specifically for TN visa holders and applicants, listing medical devices roles in Texas from employers with documented sponsorship activity. Because TN sponsorship is managed at the border or port of entry rather than through a lengthy USCIS petition process, some employers are more open to it than they would be to H-1B visa sponsorship. Searching Migrate Mate by state and visa type lets you filter directly for Texas medical devices TN opportunities without sorting through roles that do not sponsor.
Are there any Texas-specific considerations for TN sponsorship in medical devices?
Texas has several land border crossings with Mexico, which matters for Mexican nationals seeking TN status: Laredo, El Paso, and Brownsville are all active TN processing ports of entry. Canadian nationals typically process at airports. Texas also has no state income tax, which affects overall compensation calculations. Medical devices roles in Texas often require familiarity with FDA quality system regulations, and employers may ask for evidence of relevant credentials or professional licenses during the hiring process.