Medical Devices STEM OPT Jobs in Virginia
Medical devices F-1 STEM OPT sponsorship jobs in Virginia are concentrated around Northern Virginia's health tech corridor and the Richmond area, with employers including Philips, Siemens Healthineers, and Becton Dickinson actively hiring engineers and specialists. Virginia's proximity to federal health agencies and a strong biomedical research base makes it a competitive market for STEM OPT candidates in this industry.
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Location: Stuarts Draft
Department:
The salary range for this role is dependent on education & experience. $65,000-$115,000
Support the plant manufacturing facility in assuring quality products by meeting all regulatory compliance requirements of the Quality System, performing process capability studies, determining process improvements, instituting corrective action for process & Quality System deficiencies and partnering with operations in achieving both plant and GQM objectives compatible with Hollister’s Mission and Vision.
Responsibilities:
- Act as Quality Resource to help facilitate completion of assigned Change Controls.
- Lead and perform pFMEA and products/process qualifications.
- Review, evaluate and disposition non-conforming materials.
- Respond to assigned CAPAs and QNs for investigation, root cause analysis and implement solutions.
- Plan, coordinate, execute and document process capability, validation studies, and process improvement studies.
- Create, execute and conclude results for protocols, including final reports and summaries.
- Support Operations and GQM strategic plans in leading or supporting projects.
- Plan, coordinate, and document Quality Plans and work instructions.
- Conduct training on defect awareness.
- Work collaboratively with Value Stream Process Engineers to identify, investigate and solve quality issues.
- Responsible for achieving competency in all identified skill requirements outlined in associated training profile for position.
Other duties and tasks as assigned.
Essential Functions of the Role:
- Prolonged periods of sitting
- Ability to interface with a computer for long periods of time
- Frequent movement over large manufacturing floor areas
- Occasionally move products/parts from production floor into testing area, up to 20 pounds
- Travel requirements
- Ability to train/facilitate
- Flexible work schedule with start/stop times across all shifts
- Communication skills, both written and oral
Work Experience Requirements
- Number of Overall Years Necessary: 0-5 years
- Experience in Quality Engineering or equivalent industry disciplines preferred
- Experience in medical device manufacturing regarding Quality System requirements per 21 CFR 820 and/or ISO 13485 preferred
Education Requirements
- Bachelor’s Degree in Science (Engineering, Math, Natural Sciences, or related study preferred)
Specialized Skills/Technical Knowledge:
- Knowledge and application of basic statistics and experimental design preferred
- Knowledge and experience in statistical software packages preferred (ex. Minitab)
- Technical writing skill preferred.
- Experience working with self-directed work teams preferred
- Experience performing internal/external audits and evaluations preferred
- Experience with product design and product design related regulatory requirements preferred
- Knowledge and implementation of medical device Quality System requirements (FDA and ISO) preferred
- ASQ Certified Quality Engineer preferred
- Knowledge of Lean and Six Sigma Black Belt principles preferred
- Basic technical writing skills required, advanced technical writing skills preferred
- Knowledge of SAP/ERP Systems a plus
- Knowledge of Microsoft Office Products (Word, Excel, Project, Access, PowerPoint)
Local Specifications (English and Local Language):
- English
About Hollister Incorporated
Hollister Incorporated is an independent, employee-owned company that develops, manufactures and markets healthcare products worldwide. The company spearheads the advancement of innovative products for ostomy care, continence care and critical care, and also creates educational support materials for patients and healthcare professionals. Headquartered in Libertyville, Illinois, Hollister has manufacturing and distribution centers on three continents and sells in nearly 80 countries. Hollister is a wholly owned subsidiary of The Firm of John Dickinson Schneider, Inc., and is guided both by its Mission to make life more rewarding and dignified for people who use our products and services, as well as its Vision to grow and prosper as an independent, employee-owned company, and in the process, to become better human beings.
EOE Statement
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
Job Req ID: 36490
We Make Life More Rewarding and Dignified
Location: Stuarts Draft
Department:
The salary range for this role is dependent on education & experience. $65,000-$115,000
Support the plant manufacturing facility in assuring quality products by meeting all regulatory compliance requirements of the Quality System, performing process capability studies, determining process improvements, instituting corrective action for process & Quality System deficiencies and partnering with operations in achieving both plant and GQM objectives compatible with Hollister’s Mission and Vision.
Responsibilities:
- Act as Quality Resource to help facilitate completion of assigned Change Controls.
- Lead and perform pFMEA and products/process qualifications.
- Review, evaluate and disposition non-conforming materials.
- Respond to assigned CAPAs and QNs for investigation, root cause analysis and implement solutions.
- Plan, coordinate, execute and document process capability, validation studies, and process improvement studies.
- Create, execute and conclude results for protocols, including final reports and summaries.
- Support Operations and GQM strategic plans in leading or supporting projects.
- Plan, coordinate, and document Quality Plans and work instructions.
- Conduct training on defect awareness.
- Work collaboratively with Value Stream Process Engineers to identify, investigate and solve quality issues.
- Responsible for achieving competency in all identified skill requirements outlined in associated training profile for position.
Other duties and tasks as assigned.
Essential Functions of the Role:
- Prolonged periods of sitting
- Ability to interface with a computer for long periods of time
- Frequent movement over large manufacturing floor areas
- Occasionally move products/parts from production floor into testing area, up to 20 pounds
- Travel requirements
- Ability to train/facilitate
- Flexible work schedule with start/stop times across all shifts
- Communication skills, both written and oral
Work Experience Requirements
- Number of Overall Years Necessary: 0-5 years
- Experience in Quality Engineering or equivalent industry disciplines preferred
- Experience in medical device manufacturing regarding Quality System requirements per 21 CFR 820 and/or ISO 13485 preferred
Education Requirements
- Bachelor’s Degree in Science (Engineering, Math, Natural Sciences, or related study preferred)
Specialized Skills/Technical Knowledge:
- Knowledge and application of basic statistics and experimental design preferred
- Knowledge and experience in statistical software packages preferred (ex. Minitab)
- Technical writing skill preferred.
- Experience working with self-directed work teams preferred
- Experience performing internal/external audits and evaluations preferred
- Experience with product design and product design related regulatory requirements preferred
- Knowledge and implementation of medical device Quality System requirements (FDA and ISO) preferred
- ASQ Certified Quality Engineer preferred
- Knowledge of Lean and Six Sigma Black Belt principles preferred
- Basic technical writing skills required, advanced technical writing skills preferred
- Knowledge of SAP/ERP Systems a plus
- Knowledge of Microsoft Office Products (Word, Excel, Project, Access, PowerPoint)
Local Specifications (English and Local Language):
- English
About Hollister Incorporated
Hollister Incorporated is an independent, employee-owned company that develops, manufactures and markets healthcare products worldwide. The company spearheads the advancement of innovative products for ostomy care, continence care and critical care, and also creates educational support materials for patients and healthcare professionals. Headquartered in Libertyville, Illinois, Hollister has manufacturing and distribution centers on three continents and sells in nearly 80 countries. Hollister is a wholly owned subsidiary of The Firm of John Dickinson Schneider, Inc., and is guided both by its Mission to make life more rewarding and dignified for people who use our products and services, as well as its Vision to grow and prosper as an independent, employee-owned company, and in the process, to become better human beings.
EOE Statement
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
Job Req ID: 36490
STEM OPT Medical Devices Job Roles in Virginia
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Search Medical Devices Jobs in VirginiaMedical Devices STEM OPT Sponsorship Jobs in Virginia: Frequently Asked Questions
Which medical devices companies sponsor F-1 STEM OPT visas in Virginia?
Virginia-based medical devices employers with documented F-1 STEM OPT hiring patterns include Philips North America, Siemens Healthineers, Becton Dickinson, Stryker, and Medtronic, which maintain engineering and R&D operations across Northern Virginia and the Richmond corridor. Smaller contract manufacturers and health tech startups in the Dulles Technology Corridor also participate in STEM OPT programs, though sponsorship availability varies by role and business cycle.
Which cities in Virginia have the most medical devices F-1 STEM OPT sponsorship jobs?
Northern Virginia cities including McLean, Herndon, and Reston hold the highest concentration of medical devices STEM OPT roles, driven by proximity to federal health agencies and established health IT infrastructure. Richmond and Charlottesville also offer opportunities tied to academic medical centers and regional device manufacturers. Roanoke has a smaller but active cluster linked to Carilion Clinic's medical technology partnerships.
What types of medical devices roles typically qualify for F-1 STEM OPT sponsorship?
Roles qualifying for STEM OPT in medical devices generally fall under STEM-designated Classification of Instructional Programs codes, covering biomedical engineering, electrical engineering, mechanical engineering, computer science, and quality systems. Common titles include biomedical engineer, regulatory affairs specialist, hardware design engineer, software engineer for embedded systems, and quality assurance engineer. Employers must verify the role's CIP code alignment with your degree before activating STEM OPT authorization through your DSO.
How do I find medical devices F-1 STEM OPT sponsorship jobs in Virginia?
Migrate Mate filters medical devices job listings in Virginia specifically for employers with F-1 STEM OPT sponsorship history, so you can identify companies that have actively supported STEM OPT extensions rather than searching generically. Use the platform to target roles matching your degree's CIP code, then cross-reference with OFLC Wage Search to confirm prevailing wage levels for your target title and Virginia county before applying.
Are there any Virginia-specific or industry-specific considerations for F-1 STEM OPT sponsorship in medical devices?
Virginia medical devices employers subject to federal contracting requirements must be enrolled in E-Verify, which is also a mandatory condition for STEM OPT sponsorship under USCIS rules. This alignment means federally contracted device firms in Northern Virginia are structurally set up to support STEM OPT. Virginia has no state-level work authorization requirements beyond federal standards, but employers in regulated device categories may require additional background screening that can affect onboarding timelines relative to your STEM OPT start date.