Medical Devices TN Sponsorship Jobs in New York
Medical devices TN visa sponsorship jobs in New York are concentrated around Manhattan's medical corridor, Long Island's device manufacturing clusters, and the Hudson Valley. Major employers like Stryker, Becton Dickinson, and Philips Healthcare have New York operations actively hiring Canadian and Mexican professionals in engineering, regulatory affairs, and clinical roles under TN status.
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Get Access To All JobsWe are the people who give possibilities purpose
BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.
We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you’ll be supported to learn, grow and become your best self. Become a maker of possible with us.
Job Summary:
Experienced engineering resource to lead engineering projects in support of plant and company goals. Ensures compliance with BD quality systems, policies, procedures and best practices, and all local, state, federal and BD safety regulations, policies and procedures. Improve the competitiveness of the organization in a performance-based team environment. Complete projects by utilizing technical and project management skills to lead multidisciplinary teams.
Job Responsibilities: (Primary Duties, Roles, and/or Authorities)
- Provides significant leadership in managing projects related to process equipment for new products, process improvements, and multi-site initiatives.
- Ability to lead simultaneous independent engineering projects to qualify and validate new materials and suppliers.
- Perform comprehensive project planning, including justification, specification development, and budgeting.
- Design, develop, qualify, and validate manufacturing processes and tooling/equipment.
- Conceptualize and drive initiatives for continuous improvement, improved safety, cost reductions and the introduction and implementation of new technologies.
- Perform mechanical/electrical testing and gauge repeatability and reproducibility (R&R) studies.
- Statistically analyze data, including process capability and Design of Experiments (DOE).
- Trouble-shoot processes, equipment, and quality systems and develop/implement corrective and preventive actions.
- Lead problem solving activities utilizing analysis tools to identify root cause and implement robust solutions.
- Author change requests, validation documentation, technical reports and capital requisitions.
- Serve as the engineering interface with manufacturing teams, providing technical guidance and authoring operational work instructions.
- Generate and submit new project ideas and cost savings initiatives.
- Organize and effectively lead meetings.
- Assist in the coaching and development of junior engineers through example and direct guidance.
- Perform other duties as assigned.
Education and Experience:
Bachelor’s degree in engineering or other technical field of study, plus a minimum of eight (8) years engineering experience in a manufacturing environment.
Knowledge and Skills:
Basic Qualifications:
- Ability to clearly articulate ideas and information both verbally and in writing.
- Proven ability to work collaboratively within a team and contribute to team-building efforts.
- Demonstrates initiative and the ability to think independently, driving tasks and projects forward with minimal oversight.
- Capable of negotiating and making informed and timely decisions, considering various factors and potential outcomes.
- Proficiency in machinery design, including understanding mechanical principles and engineering concepts.
- Strong skills in identifying issues and developing effective solutions to resolve them.
- Knowledge of safety standards and ergonomic practices to ensure a safe and comfortable working environment.
- Ability to plan, execute, and oversee projects, ensuring they are completed on time and within budget.
- Understanding of quality management systems and processes to maintain high standards of work.
- Skills in organizing and managing logistics, ensuring efficient planning and execution of tasks.
- Proficiency in using computer software Microsoft Office applications, statistical analysis, CAD (Solidworks preferred).
- Understanding of financial principles and the ability to manage budgets and financial resources effectively.
- A working knowledge of CFR 21 Part 821 Quality System requirements and other international standards, including experience writing protocols and reports.
- Able to travel as needed.
Preferred Qualifications:
- Six Sigma Certification.
- Experience in Lean Manufacturing.
- Experience in a regulated environment.
Training Requirements:
On-the-Job, SOP’s required for position, and GMP.
Physical Demands:
- Ability to safely perform area-specific gowning procedures. These may include but are not limited to: Donning a smock with zippers and/or snaps, sitting or standing (with a safety bar) to apply shoe covers over the top of shoes, applying gloves, walking over or around benches in the transition area, and bending, stooping, and reaching motions.
- Ability to lift and move 35 lbs. (over 35 lbs. with assistance).
- Ability to utilize all area-specific PPE including but not limited to: eye protection, respiratory protection and hearing protection as required.
Work Environment:
General office and medical device manufacturing environment. May require some exposure to chemicals used in manufacturing processes. Some minor physical inconvenience or discomfort occasionally present in the work situation (moderate noise, disagreeable odors, etc.). Appropriate Personal Protective Equipment (PPE) will be provided and must be maintained by the associate.
At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.
For certain roles at BD, employment is contingent upon the Company’s receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD’s Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.
Why Join Us?
A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It’s also a place where we help each other be great, we do what’s right, we hold each other accountable, and learn and improve every day.
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you’ll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place.
Primary Work Location
USA NY - Glens Falls
Work Shift
NA (United States of America)
At BD, we reward, support and develop our associates through our comprehensive Total Rewards program. We are committed to attracting and retaining high quality talent by providing reward and recognition opportunities that promote a performance-based culture, as well as a competitive package of compensation and benefits programs. You can learn more on our career site under "Our Commitment to You."
Our salary or hourly rate ranges reward associates fairly and competitively. We regularly review these ranges and factors, such as location, contribute to the range displayed.
Our pay is based on the role and the necessary skills and education to perform it successfully. The salary or hourly rate offered is determined by the role's specific requirements, including any applicable step rate pay system at the work location. Salary or hourly pay ranges are influenced by labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location which may also affect the workplace arrangement of the role.
Salary Range Information
$92,700.00 - $152,900.00 USD Annual
Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics.
We are the people who give possibilities purpose
BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.
We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you’ll be supported to learn, grow and become your best self. Become a maker of possible with us.
Job Summary:
Experienced engineering resource to lead engineering projects in support of plant and company goals. Ensures compliance with BD quality systems, policies, procedures and best practices, and all local, state, federal and BD safety regulations, policies and procedures. Improve the competitiveness of the organization in a performance-based team environment. Complete projects by utilizing technical and project management skills to lead multidisciplinary teams.
Job Responsibilities: (Primary Duties, Roles, and/or Authorities)
- Provides significant leadership in managing projects related to process equipment for new products, process improvements, and multi-site initiatives.
- Ability to lead simultaneous independent engineering projects to qualify and validate new materials and suppliers.
- Perform comprehensive project planning, including justification, specification development, and budgeting.
- Design, develop, qualify, and validate manufacturing processes and tooling/equipment.
- Conceptualize and drive initiatives for continuous improvement, improved safety, cost reductions and the introduction and implementation of new technologies.
- Perform mechanical/electrical testing and gauge repeatability and reproducibility (R&R) studies.
- Statistically analyze data, including process capability and Design of Experiments (DOE).
- Trouble-shoot processes, equipment, and quality systems and develop/implement corrective and preventive actions.
- Lead problem solving activities utilizing analysis tools to identify root cause and implement robust solutions.
- Author change requests, validation documentation, technical reports and capital requisitions.
- Serve as the engineering interface with manufacturing teams, providing technical guidance and authoring operational work instructions.
- Generate and submit new project ideas and cost savings initiatives.
- Organize and effectively lead meetings.
- Assist in the coaching and development of junior engineers through example and direct guidance.
- Perform other duties as assigned.
Education and Experience:
Bachelor’s degree in engineering or other technical field of study, plus a minimum of eight (8) years engineering experience in a manufacturing environment.
Knowledge and Skills:
Basic Qualifications:
- Ability to clearly articulate ideas and information both verbally and in writing.
- Proven ability to work collaboratively within a team and contribute to team-building efforts.
- Demonstrates initiative and the ability to think independently, driving tasks and projects forward with minimal oversight.
- Capable of negotiating and making informed and timely decisions, considering various factors and potential outcomes.
- Proficiency in machinery design, including understanding mechanical principles and engineering concepts.
- Strong skills in identifying issues and developing effective solutions to resolve them.
- Knowledge of safety standards and ergonomic practices to ensure a safe and comfortable working environment.
- Ability to plan, execute, and oversee projects, ensuring they are completed on time and within budget.
- Understanding of quality management systems and processes to maintain high standards of work.
- Skills in organizing and managing logistics, ensuring efficient planning and execution of tasks.
- Proficiency in using computer software Microsoft Office applications, statistical analysis, CAD (Solidworks preferred).
- Understanding of financial principles and the ability to manage budgets and financial resources effectively.
- A working knowledge of CFR 21 Part 821 Quality System requirements and other international standards, including experience writing protocols and reports.
- Able to travel as needed.
Preferred Qualifications:
- Six Sigma Certification.
- Experience in Lean Manufacturing.
- Experience in a regulated environment.
Training Requirements:
On-the-Job, SOP’s required for position, and GMP.
Physical Demands:
- Ability to safely perform area-specific gowning procedures. These may include but are not limited to: Donning a smock with zippers and/or snaps, sitting or standing (with a safety bar) to apply shoe covers over the top of shoes, applying gloves, walking over or around benches in the transition area, and bending, stooping, and reaching motions.
- Ability to lift and move 35 lbs. (over 35 lbs. with assistance).
- Ability to utilize all area-specific PPE including but not limited to: eye protection, respiratory protection and hearing protection as required.
Work Environment:
General office and medical device manufacturing environment. May require some exposure to chemicals used in manufacturing processes. Some minor physical inconvenience or discomfort occasionally present in the work situation (moderate noise, disagreeable odors, etc.). Appropriate Personal Protective Equipment (PPE) will be provided and must be maintained by the associate.
At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.
For certain roles at BD, employment is contingent upon the Company’s receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD’s Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.
Why Join Us?
A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It’s also a place where we help each other be great, we do what’s right, we hold each other accountable, and learn and improve every day.
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you’ll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place.
Primary Work Location
USA NY - Glens Falls
Work Shift
NA (United States of America)
At BD, we reward, support and develop our associates through our comprehensive Total Rewards program. We are committed to attracting and retaining high quality talent by providing reward and recognition opportunities that promote a performance-based culture, as well as a competitive package of compensation and benefits programs. You can learn more on our career site under "Our Commitment to You."
Our salary or hourly rate ranges reward associates fairly and competitively. We regularly review these ranges and factors, such as location, contribute to the range displayed.
Our pay is based on the role and the necessary skills and education to perform it successfully. The salary or hourly rate offered is determined by the role's specific requirements, including any applicable step rate pay system at the work location. Salary or hourly pay ranges are influenced by labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location which may also affect the workplace arrangement of the role.
Salary Range Information
$92,700.00 - $152,900.00 USD Annual
Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics.
TN Medical Devices Job Roles in New York
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Search Medical Devices Jobs in New YorkMedical Devices TN Sponsorship Jobs in New York: Frequently Asked Questions
Which medical devices companies sponsor TN visas in New York?
Becton Dickinson (headquartered in Franklin Lakes, NJ, with significant New York operations), Stryker, Philips Healthcare, and Integra LifeSciences are among the larger medical device employers with a New York presence that have sponsored TN visas. Smaller contract manufacturers and device startups on Long Island and in the Hudson Valley also hire under TN status, particularly for engineering and quality assurance roles.
Which cities in New York have the most medical devices TN sponsorship jobs?
New York City, particularly the Manhattan and Brooklyn medical device corridors near hospital systems, sees the highest concentration of TN-eligible roles. Long Island, including Hauppauge and Melville, hosts a strong device manufacturing and R&D cluster. The Capital Region around Albany has growing regulatory and biomedical engineering activity, and the Hudson Valley has attracted device manufacturing operations tied to academic medical centers.
What types of medical devices roles typically qualify for TN sponsorship?
Roles that qualify for TN sponsorship in medical devices typically require a degree in a recognized specialty occupation field. Engineers (biomedical, mechanical, electrical, software), regulatory affairs specialists, quality engineers, and clinical application scientists are commonly approved categories. The position must require at least a bachelor's degree in a relevant discipline, and the job duties must align with the TN occupation category listed in the USMCA agreement.
How do I find medical devices TN sponsorship jobs in New York?
Migrate Mate lists medical devices jobs in New York where employers are open to TN visa sponsorship, making it easier to filter specifically for Canadian and Mexican professionals. Rather than sifting through general job postings, you can search by visa type, state, and industry on Migrate Mate to surface relevant openings at device companies with a demonstrated sponsorship history in the New York market.
Are there any New York-specific considerations for TN sponsorship in medical devices?
New York's medical devices sector is closely tied to its hospital systems and academic medical centers, which means many TN-sponsored roles involve direct collaboration with clinical environments subject to New York State Department of Health regulations. Employers in regulated device categories may require familiarity with FDA 21 CFR Part 820 quality system requirements. Canadian professionals entering at JFK or other New York ports of entry present their TN documentation directly to CBP at the port.