Medical Devices Jobs in North Carolina with F-1 OPT Sponsorship
North Carolina's medical devices sector spans the Research Triangle Park corridor, with companies like Becton Dickinson, Teleflex, and Hologic maintaining significant operations in the state. F-1 OPT candidates with engineering, biomedical science, or regulatory backgrounds will find active hiring in Raleigh, Durham, and the Charlotte metro area.
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Get Access To All JobsDate: Apr 1, 2026
Location: Morrisville, NC, US
Company: Teleflex
Expected Travel: None
Requisition ID: 13593
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.
Position Summary
Review and critique documentation for new, revised, custom, and foreign products for complete official documentation records required to manufacture medical products.
Principal Responsibilities
Responsibilities may include the following as they apply to ASK and EASK:
- Serve as Change Analyst and/or Artwork Data Manager and/or Data Steward within the PLM, VERACITI, ERP/MDG, and UDI database systems - Agile, SAP/MDG, DSD (Lansa), and VERACITI (Kallik).
- In coordination with the Engineering team, prepare new and revised product DMR and MM configurations and documentation using the required PLM, ERP/MDG, and UDI database systems - Agile, SAP/MDG, DSD.
- Manage Pilot/Prototype ECOs, Production ECOs/ECRs, Sustaining Change ECOs/ECRs, MCOs, ADCs, DMR review, SAP/Pre-Checks (MM Forms/Lansa Input Forms), SAP review, IPN and GTIN management, DSD registrations/publications.
- Review DMR-related documents and attachment files submitted for creation or changes. Standardize format, proofread for errors/clarity, and verify configuration.
- Submit documents for approval signatures, coordinate corrections and changes by approvers, and issue documentation package(s). Update appropriate personnel on open projects as required.
- Assist and communicate with Engineering, Marketing, and Regulatory in the preparation of new or revised product documentation packages. Assist in formalizing documentation, as required.
- Generate product labeling in VERACITI. Perform proofreading of product labeling in coordination with the labeling team, to ensure adherence to internal labeling procedures, accuracy, completeness, and formatting.
- Import and maintain current, accurate files for figures, graphics, and scanned images required for product labeling.
- Follow regulatory requirements, internal procedures, and the most recent and best practice guidance available in the areas of Design Control, DMR, change management, and inspection.
- Process electronic DHF documents in the PLM database. Review documents for formatting, clarity, and adherence to GDP.
- Provide other department support as required by manager.
- Adhere to and ensure the compliance of Teleflex' Code of Ethics, all Company policies, rules, procedures, and housekeeping standards.
Education / Experience Requirements
- High School Diploma or equivalent required. Bachelor’s degree preferred.
- 2+ years relevant experience. A combination of education and experience will be considered.
- Experience in regulated industry highly preferred.
- Experience with PLM (eg: Agile), ERP (eg: SAP, MDG), VERACITI (Kallik), and/or UDI (eg: Lansa) systems a plus.
Specialized Skills / Other Requirements
- Intermediate knowledge of Microsoft Suite, specifically Word and Excel.
- Solid organizational skills and attention to detail.
- Proven ability to learn and retain working knowledge of new systems and processes.
- Proven consistent performance with accuracy.
- Effective communication skills, both verbal and written.
- Proven team player and customer service oriented.
- Demonstrated sense of urgency.
- Solid and consistent ability to work in a fast-paced dynamic environment.
- Strong adaptation skills to changing priorities.
- Ability to multitask and effectively work with competing priorities with solid accuracy.
TRAVEL REQUIRED: 0 %
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: Apr 1, 2026
Location: Morrisville, NC, US
Company: Teleflex
Expected Travel: None
Requisition ID: 13593
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.
Position Summary
Review and critique documentation for new, revised, custom, and foreign products for complete official documentation records required to manufacture medical products.
Principal Responsibilities
Responsibilities may include the following as they apply to ASK and EASK:
- Serve as Change Analyst and/or Artwork Data Manager and/or Data Steward within the PLM, VERACITI, ERP/MDG, and UDI database systems - Agile, SAP/MDG, DSD (Lansa), and VERACITI (Kallik).
- In coordination with the Engineering team, prepare new and revised product DMR and MM configurations and documentation using the required PLM, ERP/MDG, and UDI database systems - Agile, SAP/MDG, DSD.
- Manage Pilot/Prototype ECOs, Production ECOs/ECRs, Sustaining Change ECOs/ECRs, MCOs, ADCs, DMR review, SAP/Pre-Checks (MM Forms/Lansa Input Forms), SAP review, IPN and GTIN management, DSD registrations/publications.
- Review DMR-related documents and attachment files submitted for creation or changes. Standardize format, proofread for errors/clarity, and verify configuration.
- Submit documents for approval signatures, coordinate corrections and changes by approvers, and issue documentation package(s). Update appropriate personnel on open projects as required.
- Assist and communicate with Engineering, Marketing, and Regulatory in the preparation of new or revised product documentation packages. Assist in formalizing documentation, as required.
- Generate product labeling in VERACITI. Perform proofreading of product labeling in coordination with the labeling team, to ensure adherence to internal labeling procedures, accuracy, completeness, and formatting.
- Import and maintain current, accurate files for figures, graphics, and scanned images required for product labeling.
- Follow regulatory requirements, internal procedures, and the most recent and best practice guidance available in the areas of Design Control, DMR, change management, and inspection.
- Process electronic DHF documents in the PLM database. Review documents for formatting, clarity, and adherence to GDP.
- Provide other department support as required by manager.
- Adhere to and ensure the compliance of Teleflex' Code of Ethics, all Company policies, rules, procedures, and housekeeping standards.
Education / Experience Requirements
- High School Diploma or equivalent required. Bachelor’s degree preferred.
- 2+ years relevant experience. A combination of education and experience will be considered.
- Experience in regulated industry highly preferred.
- Experience with PLM (eg: Agile), ERP (eg: SAP, MDG), VERACITI (Kallik), and/or UDI (eg: Lansa) systems a plus.
Specialized Skills / Other Requirements
- Intermediate knowledge of Microsoft Suite, specifically Word and Excel.
- Solid organizational skills and attention to detail.
- Proven ability to learn and retain working knowledge of new systems and processes.
- Proven consistent performance with accuracy.
- Effective communication skills, both verbal and written.
- Proven team player and customer service oriented.
- Demonstrated sense of urgency.
- Solid and consistent ability to work in a fast-paced dynamic environment.
- Strong adaptation skills to changing priorities.
- Ability to multitask and effectively work with competing priorities with solid accuracy.
TRAVEL REQUIRED: 0 %
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.
Job Roles in Medical Devices in North Carolina
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Get Access To All JobsFrequently Asked Questions
Which medical devices companies sponsor F-1 OPT visas in North Carolina?
North Carolina hosts several established medical devices employers with histories of hiring F-1 OPT candidates, including Becton Dickinson in Sumter, Teleflex in Morrisville, and Hologic in Marlborough. Larger companies generally have structured international hiring processes, while mid-sized contract manufacturers in the Research Triangle Park area also hire OPT candidates in engineering and quality roles. Sponsorship availability varies by role and department.
Which cities in North Carolina have the most medical devices F-1 OPT sponsorship jobs?
Raleigh, Durham, and Research Triangle Park collectively represent the highest concentration of medical devices F-1 OPT jobs in North Carolina, driven by the density of life sciences companies and proximity to NC State, Duke, and UNC-Chapel Hill. Charlotte is a secondary market with growing activity in device manufacturing and regulatory affairs. Morrisville and Cary also have notable employer presence.
What types of medical devices roles typically qualify for F-1 OPT sponsorship?
Roles that align closely with a STEM degree field are the strongest candidates for F-1 OPT authorization in medical devices. These commonly include biomedical engineering, quality engineering, regulatory affairs, R&D, manufacturing engineering, and software engineering for embedded or device systems. Positions requiring a bachelor's or higher in a directly related technical field tend to be most straightforward for OPT work authorization alignment.
How do I find medical devices F-1 OPT sponsorship jobs in North Carolina?
Migrate Mate is built specifically for international students and filters jobs by visa type and state, making it straightforward to browse medical devices roles in North Carolina that employers have indicated as OPT-eligible. Rather than sorting through general job boards, Migrate Mate surfaces sponsorship-relevant postings so you can focus on companies actively open to F-1 OPT candidates in the state's medical devices sector.
Are there any state-specific or industry-specific considerations for F-1 OPT in North Carolina's medical devices sector?
North Carolina has a concentrated life sciences ecosystem around Research Triangle Park, which means many employers are familiar with international hiring and OPT work authorization. STEM OPT extension eligibility is a key consideration, as medical devices roles in engineering and science fields commonly qualify for the 24-month STEM extension beyond the standard 12 months. Students should confirm their degree and role align with the STEM OPT designated degree list before applying.
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