Medical Devices TN Sponsorship Jobs in Massachusetts
Massachusetts is one of the top states for medical devices TN visa sponsorship, anchored by major employers like Boston Scientific, Stryker, and Medtronic across the Greater Boston corridor and MetroWest region. Canadian and Mexican professionals in engineering, regulatory affairs, and scientific roles will find concentrated opportunities in a state that houses hundreds of device and diagnostics companies.
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Get Access To All JobsRecruiter: Spencer Gregory Hale
Senior Supplier Quality Engineer – External Operations Acquisition
Remote Eligible: Hybrid
Onsite Location(s): Marlborough, MA; Minneapolis, MN
About the role:
The External Operations (ExOps) organization at Boston Scientific is a global, passionate team that oversees a diverse network of suppliers which manufacture finished devices for BSC distribution. The Senior Supplier Quality Engineer will demonstrate a primary commitment to patient safety and collaborate with cross-functional internal/external resources to continually improve our supplier’s manufacturing processes. In this role, you will support Sourced Finished Medical Device (SFMD) products within a newly acquired company within the Neuromodulation division, with a primary focus on Single-Use Devices and capital equipment.
Your responsibilities include:
Sustaining Engineering:
- Evaluates and communicates quality issues to suppliers and applies sound, systematic problem-solving methodologies in identifying, prioritizing, and resolving quality issues. Reviews and approves supplier corrective action plans and verification of effectiveness documentation.
- Proactively assesses supplier capabilities through direct on-site visits and technical discussions. Coordinates the evaluation of proposed changes at suppliers.
- Plans and leads supplier audits to assess compliance with regulatory standards and Boston Scientific requirements, including audit scheduling investigation, and evaluation of audit observation and findings, reporting, follow-up, and confirmation of follow-up actions.
- Manages sustaining quality issues, process change impacts, and design change implementations for suppliers within the Acquired Entity Quality system, the hybridized BSC-Acquired Entity Quality System, and in the BSC Quality System after products are successfully integrated.
- Investigates and solves non-conformances due to incoming inspection at BSC Distribution Centers.
- Supports Design Quality Assurance with Field Action and Product Inquiry Reports by performing investigations on supplier-related or supplier-caused quality issues.
- Investigates complaints and manages NCEPs at OEM suppliers and CM suppliers where the issue is manufacturing-related.
- Supports Supplier Change Impact Assessments for process changes at suppliers.
- Supports and performs Finished Good Documentation changes in support of ongoing design changes or labeling updates.
- Leads projects and consistently hits project milestones. Creates crisp and clear project plans and develops strong contingency plans as part of project planning process.
New Product Development:
- Lead strategy and execute initial onboarding deliverables to support initial distribution of Acquired Entity’s products through BSC Distribution Centers.
- Lead the execution of SFMD quality deliverables and collaborate with cross-functional new product development teams to onboard finished medical device suppliers.
- Generate and review quality plans, agreements, product specifications, component qualifications, design verification/validations, and process validations.
Quality System Champion:
- Supports Material Controls external regulatory body audits requests as required.
- Collaborates with corporate and regional supplier quality organizations on policy, procedure, and guideline development. Includes generation, review, and implementation of these documents.
- Identifies and advises management on potential improvements to quality systems and processes in the company.
- Champions 100% compliance to company policies and SOP’s.
What we’re looking for in you:
Minimal Qualifications:
- BS degree in engineering or technical field with minimum of 5 years of relevant experience in quality engineering.
- Experience in medical device, automotive, aeronautical, semiconductor, or other regulated industry.
- Project management: ability to influence cross functional global teams spanning Quality, Operations, R&D, and Sourcing.
- Experience in process validation, design controls, risk management, CAPA, SCAR.
- Ability to work independently; organized and self-driven.
- Articulate communicator; adept at packaging and appropriately scaling information to the intended audience.
- Ability to rapidly learn and use new software applications (e.g., PLM, ERP).
- Domestic and international travel up to 25%.
Preferred Qualifications:
- 7+ years of medical device engineering experience preferred.
- Medical Device Industry experience.
- Problem Solving and Project Management experience.
- Leadership experience on a materials or service commodity team.
- Lead auditor of quality systems experience (ISO 13485 or similar).
- ASQ certification (CQE, CBA, SSGB, SSBB) desired.
Requisition ID: 632059
Minimum Salary: $ 89200
Maximum Salary: $ 169500
The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) – see www.bscbenefitsconnect.com—will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above.
Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).
Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).
For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.
Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.
Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.
Recruiter: Spencer Gregory Hale
Senior Supplier Quality Engineer – External Operations Acquisition
Remote Eligible: Hybrid
Onsite Location(s): Marlborough, MA; Minneapolis, MN
About the role:
The External Operations (ExOps) organization at Boston Scientific is a global, passionate team that oversees a diverse network of suppliers which manufacture finished devices for BSC distribution. The Senior Supplier Quality Engineer will demonstrate a primary commitment to patient safety and collaborate with cross-functional internal/external resources to continually improve our supplier’s manufacturing processes. In this role, you will support Sourced Finished Medical Device (SFMD) products within a newly acquired company within the Neuromodulation division, with a primary focus on Single-Use Devices and capital equipment.
Your responsibilities include:
Sustaining Engineering:
- Evaluates and communicates quality issues to suppliers and applies sound, systematic problem-solving methodologies in identifying, prioritizing, and resolving quality issues. Reviews and approves supplier corrective action plans and verification of effectiveness documentation.
- Proactively assesses supplier capabilities through direct on-site visits and technical discussions. Coordinates the evaluation of proposed changes at suppliers.
- Plans and leads supplier audits to assess compliance with regulatory standards and Boston Scientific requirements, including audit scheduling investigation, and evaluation of audit observation and findings, reporting, follow-up, and confirmation of follow-up actions.
- Manages sustaining quality issues, process change impacts, and design change implementations for suppliers within the Acquired Entity Quality system, the hybridized BSC-Acquired Entity Quality System, and in the BSC Quality System after products are successfully integrated.
- Investigates and solves non-conformances due to incoming inspection at BSC Distribution Centers.
- Supports Design Quality Assurance with Field Action and Product Inquiry Reports by performing investigations on supplier-related or supplier-caused quality issues.
- Investigates complaints and manages NCEPs at OEM suppliers and CM suppliers where the issue is manufacturing-related.
- Supports Supplier Change Impact Assessments for process changes at suppliers.
- Supports and performs Finished Good Documentation changes in support of ongoing design changes or labeling updates.
- Leads projects and consistently hits project milestones. Creates crisp and clear project plans and develops strong contingency plans as part of project planning process.
New Product Development:
- Lead strategy and execute initial onboarding deliverables to support initial distribution of Acquired Entity’s products through BSC Distribution Centers.
- Lead the execution of SFMD quality deliverables and collaborate with cross-functional new product development teams to onboard finished medical device suppliers.
- Generate and review quality plans, agreements, product specifications, component qualifications, design verification/validations, and process validations.
Quality System Champion:
- Supports Material Controls external regulatory body audits requests as required.
- Collaborates with corporate and regional supplier quality organizations on policy, procedure, and guideline development. Includes generation, review, and implementation of these documents.
- Identifies and advises management on potential improvements to quality systems and processes in the company.
- Champions 100% compliance to company policies and SOP’s.
What we’re looking for in you:
Minimal Qualifications:
- BS degree in engineering or technical field with minimum of 5 years of relevant experience in quality engineering.
- Experience in medical device, automotive, aeronautical, semiconductor, or other regulated industry.
- Project management: ability to influence cross functional global teams spanning Quality, Operations, R&D, and Sourcing.
- Experience in process validation, design controls, risk management, CAPA, SCAR.
- Ability to work independently; organized and self-driven.
- Articulate communicator; adept at packaging and appropriately scaling information to the intended audience.
- Ability to rapidly learn and use new software applications (e.g., PLM, ERP).
- Domestic and international travel up to 25%.
Preferred Qualifications:
- 7+ years of medical device engineering experience preferred.
- Medical Device Industry experience.
- Problem Solving and Project Management experience.
- Leadership experience on a materials or service commodity team.
- Lead auditor of quality systems experience (ISO 13485 or similar).
- ASQ certification (CQE, CBA, SSGB, SSBB) desired.
Requisition ID: 632059
Minimum Salary: $ 89200
Maximum Salary: $ 169500
The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) – see www.bscbenefitsconnect.com—will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above.
Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).
Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).
For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.
Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.
Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.
TN Medical Devices Job Roles in Massachusetts
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Search Medical Devices Jobs in MassachusettsMedical Devices TN Sponsorship Jobs in Massachusetts: Frequently Asked Questions
Which medical devices companies sponsor TN visas in Massachusetts?
Massachusetts hosts a deep concentration of medical device employers with documented TN visa sponsorship activity. Boston Scientific (headquartered in Marlborough), Stryker, Hologic, Insulet, and Haemonetics are among the larger employers in the state. Many mid-size and startup device companies in the Route 128 and Route 495 corridors also sponsor TN workers, particularly in engineering, quality assurance, and regulatory affairs functions.
Which cities in Massachusetts have the most medical devices TN sponsorship jobs?
Greater Boston and the MetroWest suburbs account for the majority of medical devices TN roles in Massachusetts. Marlborough, Natick, Waltham, Woburn, and Burlington have significant device company footprints, while Boston and Cambridge attract roles tied to hospital systems and medtech startups. Tewksbury and Billerica also have established device manufacturing and R&D operations with recurring hiring needs.
What types of medical devices roles typically qualify for TN sponsorship?
TN-eligible roles in medical devices generally fall under occupational categories recognized in the USMCA, including engineers (mechanical, electrical, biomedical, software), scientific professionals (chemists, biologists), computer systems analysts, and management consultants. Roles in regulatory affairs, quality systems, and clinical applications may qualify depending on the specific job duties and the applicant's degree field. Each petition is assessed on its own facts, so the job description and educational credentials both matter.
How do I find medical devices TN sponsorship jobs in Massachusetts?
Migrate Mate is purpose-built for international job seekers who need TN visa sponsorship and filters specifically for roles where employers have sponsored TN workers before. To find medical devices TN jobs in Massachusetts, browse Migrate Mate's filtered listings by state, visa type, and industry. This saves time compared to manually screening general job postings where sponsorship willingness is rarely stated upfront.
Are there any Massachusetts-specific considerations for TN sponsorship in medical devices?
Massachusetts has strong state-level employment protections, including non-compete restrictions that are narrower than in many other states, which can matter when evaluating offer letters. The state's large academic medical center network (Mass General Brigham, Beth Israel Deaconess) sometimes creates hybrid device and clinical roles where TN eligibility depends closely on how the position is classified. Device employers in Massachusetts tend to be familiar with TN processes given the high concentration of Canadian engineering talent in the region.