Medical Devices F-1 STEM OPT Sponsorship Jobs in Pennsylvania
Pennsylvania's medical devices sector spans the Philadelphia suburbs, Pittsburgh, and the Lehigh Valley, with employers like Siemens Healthineers, West Pharmaceutical Services, and Integra LifeSciences filing F-1 STEM OPT extensions for engineers, quality specialists, and R&D scientists. The state's concentration of device manufacturers and research hospitals makes it a strong market for OPT students seeking STEM OPT sponsorship.
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Get Access To All JobsDate: May 1, 2026
Location: Wyomissing, PA, US
Company: Teleflex
Expected Travel: Up to 25%
Requisition ID: 13761
About Teleflex Incorporated
As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare.
Teleflex is the home of Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ – trusted brands united by a common sense of purpose.
At Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com.
Vascular & Emergency Medicine
Built on a legacy of innovation and clinical excellence, the Vascular & Emergency Medicine business at Teleflex develops and delivers advanced medical technologies that empower clinicians to help improve patient outcomes and optimize healthcare efficiency. Our trusted Arrow™, EZ-IO™, and QuikClot™ brands set the standard for vascular access and emergency medicine, offering proven solutions to enhance patient outcomes. From technically advanced vascular access devices – including central venous and arterial catheters, PICCs, and sheath introducers with antimicrobial protection – to life-saving intraosseous access systems and hemostatic technologies used by hospitals, EMS, and military teams worldwide, our portfolio embodies precision, reliability, and performance. As part of a high-performing, purpose-driven organization, we are united by a commitment to clinical differentiation, innovation, and excellence. Join a dynamic, growth-focused team that offers advanced medical technology solutions that make a lasting impact on healthcare.
Position Summary
Teleflex is a global provider of medical technologies designed to improve the health and quality of people’s lives. We apply purpose driven innovation – a relentless pursuit of identifying unmet clinical needs – to benefit patients and healthcare providers. Our portfolio is diverse, with solutions in the fields of vascular and interventional access, surgical, cardiac care, emergency medicine and respiratory care. Teleflex employees worldwide are united in the understanding that what we do every day makes a difference.
This position is responsible for the project management of new product development initiatives through a methodical approach of planning, executing and controlling projects from start to finish. The PM demonstrates program ownership and guides teams through project execution process while translating strategic objectives to an execution level. The PM ensures consistent and compliant practices throughout all phases of the project life cycle and across functional teams. Use professional project management concepts and frameworks in accordance with company objectives to solve complex problems in a creative and effective way. Exercise a balance of independent judgment and group organization in developing methods, techniques, and evaluation criteria for obtaining results.
Principal Responsibilities
- Lead either Sustaining, New Product Development, or some combination of opportunities defined by business need
- Responsible for planning and managing global and/or local product development initiatives of medical devices for the Vascular business unit.
- Effectively lead and drive project teams in a collaborative environment, completing project deliverables per target timelines and requirements.
- Maintain and monitor project budgets, directing the efficient use of resources to effectively complete projects.
- Lead project-related activities of project team members, providing guidance on conformance to established design control procedures.
- Provide leadership for the project team by building and motivating team members to meet project goals and milestones.
- Lead, coordinate and facilitate weekly meetings, action items, and follow-up with subject matter experts on expected deliverables.
- Prepare project summary reports, develop project plans, identifies risk and communicates mitigation activities.
- Prepare and deliver project status presentations to Management regularly.
- Partner with Technical and Marketing leads for portfolio management of specific product family management.
- Lead business gating process for projects under his/her responsibility.
- Lead and/or participate in all phases of development, starting with concept through post-market surveillance.
- Negotiate and resolve any conflicts and drive decisions among team / functional members to accomplish project and business goals.
- Define project resource requirements and negotiate with functional managers to obtain resources necessary to support assigned programs.
- Adhere to all regulatory agency standards, company quality standards and corporate policies.
- Must be able to travel domestically and internationally as business needs demand.
Education / Experience Requirements
- BS in technical discipline (i.e. engineering, bio-science), advanced degree preferred.
- Minimum of 3 (preferred 5+) years of demonstrated experience in project/program management working in a technical discipline, medical device and/or engineering preferred.
- PMP certified is desirable.
- Proficient in the development process and standards of medical devices, at a minimum proficiency with design control standards is required.
- Demonstrated experience leading projects of complex systems with multiple partners.
- Proficiency in Microsoft Office, specifically Microsoft Project, Powerpoint, Sharepoint/MS Teams.
- Proficiency in Smartsheet is desirable.
Specialized Skills / Other Requirements
- Knowledgable of lifecycle management planning, requirements and implementation.
- Demonstrated customer relations, presentation, problem solving, and negotiation skills.
- Excellent leadership and communication skills a MUST.
- Self-starter with strong proactive work ethic, well-organized and detail-oriented.
- Proven ability to influence across functions, drive collaboration, and lead change.
- Knowledgable of software development and experience with Agile and Scrum project methodology desired.
- Technical aptitude and displayed ability to grasp general knowledge of multiple disciplines and technologies.
- Ability to support multiple projects and balance priorities, work independently or collaboratively to determine and develop solutions.
Working Conditions / Physical Demands
TRAVEL REQUIRED: 15%
WORKING ENVIRONMENT:
- Office/Professional Plant/Manufacturing Remote/Field Laboratory
At Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front.
Teleflex Incorporated is an equal opportunity employer. Applicants will be considered without regard to age, race, religion, color, national origin, ancestry, sexual orientation, disability, nationality, sex, or veteran status. If you require accommodation to apply for a position, please contact us at: 877-880-8588 or Talent@Teleflex.com.
Teleflex, the Teleflex logo, Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries.
© 2026 Teleflex Incorporated. All rights reserved.
Date: May 1, 2026
Location: Wyomissing, PA, US
Company: Teleflex
Expected Travel: Up to 25%
Requisition ID: 13761
About Teleflex Incorporated
As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare.
Teleflex is the home of Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ – trusted brands united by a common sense of purpose.
At Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com.
Vascular & Emergency Medicine
Built on a legacy of innovation and clinical excellence, the Vascular & Emergency Medicine business at Teleflex develops and delivers advanced medical technologies that empower clinicians to help improve patient outcomes and optimize healthcare efficiency. Our trusted Arrow™, EZ-IO™, and QuikClot™ brands set the standard for vascular access and emergency medicine, offering proven solutions to enhance patient outcomes. From technically advanced vascular access devices – including central venous and arterial catheters, PICCs, and sheath introducers with antimicrobial protection – to life-saving intraosseous access systems and hemostatic technologies used by hospitals, EMS, and military teams worldwide, our portfolio embodies precision, reliability, and performance. As part of a high-performing, purpose-driven organization, we are united by a commitment to clinical differentiation, innovation, and excellence. Join a dynamic, growth-focused team that offers advanced medical technology solutions that make a lasting impact on healthcare.
Position Summary
Teleflex is a global provider of medical technologies designed to improve the health and quality of people’s lives. We apply purpose driven innovation – a relentless pursuit of identifying unmet clinical needs – to benefit patients and healthcare providers. Our portfolio is diverse, with solutions in the fields of vascular and interventional access, surgical, cardiac care, emergency medicine and respiratory care. Teleflex employees worldwide are united in the understanding that what we do every day makes a difference.
This position is responsible for the project management of new product development initiatives through a methodical approach of planning, executing and controlling projects from start to finish. The PM demonstrates program ownership and guides teams through project execution process while translating strategic objectives to an execution level. The PM ensures consistent and compliant practices throughout all phases of the project life cycle and across functional teams. Use professional project management concepts and frameworks in accordance with company objectives to solve complex problems in a creative and effective way. Exercise a balance of independent judgment and group organization in developing methods, techniques, and evaluation criteria for obtaining results.
Principal Responsibilities
- Lead either Sustaining, New Product Development, or some combination of opportunities defined by business need
- Responsible for planning and managing global and/or local product development initiatives of medical devices for the Vascular business unit.
- Effectively lead and drive project teams in a collaborative environment, completing project deliverables per target timelines and requirements.
- Maintain and monitor project budgets, directing the efficient use of resources to effectively complete projects.
- Lead project-related activities of project team members, providing guidance on conformance to established design control procedures.
- Provide leadership for the project team by building and motivating team members to meet project goals and milestones.
- Lead, coordinate and facilitate weekly meetings, action items, and follow-up with subject matter experts on expected deliverables.
- Prepare project summary reports, develop project plans, identifies risk and communicates mitigation activities.
- Prepare and deliver project status presentations to Management regularly.
- Partner with Technical and Marketing leads for portfolio management of specific product family management.
- Lead business gating process for projects under his/her responsibility.
- Lead and/or participate in all phases of development, starting with concept through post-market surveillance.
- Negotiate and resolve any conflicts and drive decisions among team / functional members to accomplish project and business goals.
- Define project resource requirements and negotiate with functional managers to obtain resources necessary to support assigned programs.
- Adhere to all regulatory agency standards, company quality standards and corporate policies.
- Must be able to travel domestically and internationally as business needs demand.
Education / Experience Requirements
- BS in technical discipline (i.e. engineering, bio-science), advanced degree preferred.
- Minimum of 3 (preferred 5+) years of demonstrated experience in project/program management working in a technical discipline, medical device and/or engineering preferred.
- PMP certified is desirable.
- Proficient in the development process and standards of medical devices, at a minimum proficiency with design control standards is required.
- Demonstrated experience leading projects of complex systems with multiple partners.
- Proficiency in Microsoft Office, specifically Microsoft Project, Powerpoint, Sharepoint/MS Teams.
- Proficiency in Smartsheet is desirable.
Specialized Skills / Other Requirements
- Knowledgable of lifecycle management planning, requirements and implementation.
- Demonstrated customer relations, presentation, problem solving, and negotiation skills.
- Excellent leadership and communication skills a MUST.
- Self-starter with strong proactive work ethic, well-organized and detail-oriented.
- Proven ability to influence across functions, drive collaboration, and lead change.
- Knowledgable of software development and experience with Agile and Scrum project methodology desired.
- Technical aptitude and displayed ability to grasp general knowledge of multiple disciplines and technologies.
- Ability to support multiple projects and balance priorities, work independently or collaboratively to determine and develop solutions.
Working Conditions / Physical Demands
TRAVEL REQUIRED: 15%
WORKING ENVIRONMENT:
- Office/Professional Plant/Manufacturing Remote/Field Laboratory
At Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front.
Teleflex Incorporated is an equal opportunity employer. Applicants will be considered without regard to age, race, religion, color, national origin, ancestry, sexual orientation, disability, nationality, sex, or veteran status. If you require accommodation to apply for a position, please contact us at: 877-880-8588 or Talent@Teleflex.com.
Teleflex, the Teleflex logo, Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries.
© 2026 Teleflex Incorporated. All rights reserved.
Medical Devices Job Roles in Pennsylvania
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Search Medical Devices Jobs in PennsylvaniaMedical Devices Jobs in Pennsylvania: Frequently Asked Questions
Which medical devices companies sponsor F-1 STEM OPT visas in Pennsylvania?
Pennsylvania-based medical devices employers with documented F-1 STEM OPT sponsorship activity include Siemens Healthineers in Malvern, West Pharmaceutical Services in Exton, Integra LifeSciences in Princeton Pike corridor facilities, and several contract manufacturers in the Philadelphia suburbs. Large device companies with established immigration programs and E-Verify enrollment are generally better positioned to support STEM OPT extensions, though sponsorship decisions vary by role, department, and headcount at the time of hiring.
Which cities in Pennsylvania have the most medical devices F-1 STEM OPT sponsorship jobs?
The Philadelphia metropolitan area, including Chester County suburbs like Malvern, Exton, and Wayne, concentrates the highest density of medical devices employers in Pennsylvania. Pittsburgh supports biomedical device roles tied to UPMC and Carnegie Mellon University spin-offs. The Lehigh Valley, particularly Allentown and Bethlehem, hosts contract device manufacturers. Students targeting STEM OPT sponsorship typically find the broadest hiring activity in the southeastern Pennsylvania corridor.
What types of medical devices roles typically qualify for F-1 STEM OPT sponsorship?
Roles that regularly qualify include biomedical engineering, mechanical engineering, electrical engineering, quality assurance engineering, regulatory affairs, manufacturing engineering, and R&D scientist positions. These roles typically carry SOC codes classified as STEM occupations under the DHS STEM Designated Degree Program List, which is the eligibility criterion for STEM OPT extension. Roles that are primarily administrative, sales, or non-technical generally do not qualify, so confirming your specific job title and SOC code with your DSO before accepting an offer is important.
How do I find medical devices F-1 STEM OPT sponsorship jobs in Pennsylvania?
Migrate Mate filters job listings specifically by visa type and industry, making it straightforward to search for medical devices roles in Pennsylvania where employers have F-1 STEM OPT sponsorship history. You can narrow results to Pennsylvania locations and STEM-eligible positions rather than manually screening general postings. Supplementing your search by reviewing DOL Labor Condition Application filings through OFLC Wage Search can also confirm which Pennsylvania device employers have recent sponsorship activity for STEM roles.
Are there any Pennsylvania-specific or medical devices industry considerations for F-1 STEM OPT sponsorship?
Pennsylvania medical devices employers are subject to FDA device manufacturing regulations, which creates demand for quality and regulatory roles but also means many positions require familiarity with QMS frameworks like ISO 13485 and 21 CFR Part 820. Employers must be enrolled in E-Verify to sponsor STEM OPT extensions, and larger device companies in the state with established HR and immigration compliance teams tend to have more predictable onboarding processes for OPT students. Pennsylvania has no state-level immigration requirements beyond federal STEM OPT rules.