Medical Devices F-1 STEM OPT Sponsorship Jobs in Delaware
Medical devices F-1 STEM OPT sponsorship jobs in Delaware draw from a concentrated cluster of life sciences employers near Wilmington, including Incyte, AstraZeneca, and contract device manufacturers along the Route 202 corridor. Roles in biomedical engineering, quality systems, and regulatory affairs are common entry points for STEM OPT candidates at these organizations.
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Get Access To All JobsINTRODUCTION
Hologic is seeking a Systems Engineer to join our Research and Development team in Newark, Delaware. In this role, you will contribute to the development of advanced medical imaging systems and electromechanical subsystems that help improve clinical outcomes. This position requires regular onsite presence in Newark, DE to collaborate closely with cross‑functional engineering teams and support hands‑on system integration, testing, and troubleshooting.
You will work alongside electrical, mechanical, and software engineers, scientists, and product owners to support the design, integration, verification, and validation of medical imaging technologies.
KEY RESPONSIBILITIES
- Contribute to the specification, design, component selection, system integration, verification, and validation of medical imaging systems and electromechanical subsystems.
- Develop an in‑depth understanding of system architecture design and clinical use of medical imaging systems.
- Propose system definitions and specifications to meet customer requirements and user needs.
- Support concept development, specification, and design of new medical imaging products.
- Implement new electromechanical designs and modifications within defined cost, schedule, and performance targets.
- Maintain traceability between system requirements and subsystem requirements.
- Maintain traceability between product requirements, identified risks, and mitigation strategies.
- Perform hands‑on troubleshooting at system and subsystem levels.
- Support engineering teams and system quality assurance through concept, implementation, and verification phases.
- Collaborate with design engineers to define test methods and conditions.
- Complete design documentation and Engineering Change Orders in accordance with Hologic procedures and best practices.
- Create project schedules, track progress, and report status or issues to management and project teams.
- Support design transfer to manufacturing.
- Establish collaborative relationships with stakeholders across the division.
- Manage multiple projects concurrently under supervision.
- Continue to build technical expertise and professional development, contributing to innovative problem‑solving and product development.
QUALIFICATIONS
Education
- Bachelor’s degree in Systems Engineering, Biomedical Engineering, Electrical Engineering, Mechanical Engineering, Computer Science, or a related technical discipline.
Experience
Preferred minimum:
- 1–2 years of experience with a technical bachelor’s degree, or
- 0–2 years with a master’s degree.
Skills and Knowledge
- Understanding of systems engineering methodologies.
- Experience with electromechanical design and embedded software development, ideally within the medical device field.
- Experience with systems integration across electrical, mechanical, and software components.
- Knowledge across multiple engineering disciplines.
- Strong critical thinking, analytical, and problem‑solving skills.
- Familiarity with physical and mathematical modeling tools.
- Knowledge of medical device regulations and standards, including: FDA QSR, ISO 13485, ISO 14971, IEC 60601‑1 and IEC 60601‑1‑2, IEC 62304 (software lifecycle for medical devices).
- Experience with Product Lifecycle Management (PLM) systems.
- Strong communication, teamwork, and collaboration skills.
- Experience with technical documentation and presentations.
- Project management skills.
- SolidWorks experience is a plus.
COMPENSATION
- The annualized base salary range for this role $78,000 - $122,100 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, geography, education, business needs and market demand.
Agency and Third‑Party Recruiter Notice: Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition, Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered.
As part of our commitment to a fair and accurate evaluation of each candidate's qualifications, we require all applicants to refrain from using AI tools, such as generative AI or automated writing assistance, during any stage of the interview process. Responses influenced by AI may result in disqualification. We appreciate your understanding and cooperation in ensuring a transparent and equitable selection process.
Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans.
INTRODUCTION
Hologic is seeking a Systems Engineer to join our Research and Development team in Newark, Delaware. In this role, you will contribute to the development of advanced medical imaging systems and electromechanical subsystems that help improve clinical outcomes. This position requires regular onsite presence in Newark, DE to collaborate closely with cross‑functional engineering teams and support hands‑on system integration, testing, and troubleshooting.
You will work alongside electrical, mechanical, and software engineers, scientists, and product owners to support the design, integration, verification, and validation of medical imaging technologies.
KEY RESPONSIBILITIES
- Contribute to the specification, design, component selection, system integration, verification, and validation of medical imaging systems and electromechanical subsystems.
- Develop an in‑depth understanding of system architecture design and clinical use of medical imaging systems.
- Propose system definitions and specifications to meet customer requirements and user needs.
- Support concept development, specification, and design of new medical imaging products.
- Implement new electromechanical designs and modifications within defined cost, schedule, and performance targets.
- Maintain traceability between system requirements and subsystem requirements.
- Maintain traceability between product requirements, identified risks, and mitigation strategies.
- Perform hands‑on troubleshooting at system and subsystem levels.
- Support engineering teams and system quality assurance through concept, implementation, and verification phases.
- Collaborate with design engineers to define test methods and conditions.
- Complete design documentation and Engineering Change Orders in accordance with Hologic procedures and best practices.
- Create project schedules, track progress, and report status or issues to management and project teams.
- Support design transfer to manufacturing.
- Establish collaborative relationships with stakeholders across the division.
- Manage multiple projects concurrently under supervision.
- Continue to build technical expertise and professional development, contributing to innovative problem‑solving and product development.
QUALIFICATIONS
Education
- Bachelor’s degree in Systems Engineering, Biomedical Engineering, Electrical Engineering, Mechanical Engineering, Computer Science, or a related technical discipline.
Experience
Preferred minimum:
- 1–2 years of experience with a technical bachelor’s degree, or
- 0–2 years with a master’s degree.
Skills and Knowledge
- Understanding of systems engineering methodologies.
- Experience with electromechanical design and embedded software development, ideally within the medical device field.
- Experience with systems integration across electrical, mechanical, and software components.
- Knowledge across multiple engineering disciplines.
- Strong critical thinking, analytical, and problem‑solving skills.
- Familiarity with physical and mathematical modeling tools.
- Knowledge of medical device regulations and standards, including: FDA QSR, ISO 13485, ISO 14971, IEC 60601‑1 and IEC 60601‑1‑2, IEC 62304 (software lifecycle for medical devices).
- Experience with Product Lifecycle Management (PLM) systems.
- Strong communication, teamwork, and collaboration skills.
- Experience with technical documentation and presentations.
- Project management skills.
- SolidWorks experience is a plus.
COMPENSATION
- The annualized base salary range for this role $78,000 - $122,100 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, geography, education, business needs and market demand.
Agency and Third‑Party Recruiter Notice: Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition, Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered.
As part of our commitment to a fair and accurate evaluation of each candidate's qualifications, we require all applicants to refrain from using AI tools, such as generative AI or automated writing assistance, during any stage of the interview process. Responses influenced by AI may result in disqualification. We appreciate your understanding and cooperation in ensuring a transparent and equitable selection process.
Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans.
Medical Devices Job Roles in Delaware
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Search Medical Devices Jobs in DelawareMedical Devices Jobs in Delaware: Frequently Asked Questions
Which medical devices companies sponsor F-1 STEM OPT visas in Delaware?
Delaware's medical devices and life sciences sector includes employers such as Incyte, AstraZeneca's Wilmington operations, and contract development and manufacturing organizations along the Route 202 corridor. Device-adjacent firms in quality assurance, regulatory affairs, and biomedical engineering have a documented history of filing Labor Condition Applications for STEM-designated roles, making them worth prioritizing in your job search.
Which cities in Delaware have the most medical devices F-1 STEM OPT sponsorship jobs?
Wilmington concentrates the largest share of Delaware's medical devices and life sciences employment, particularly in the Brandywine Valley area where pharmaceutical and device companies cluster. Newark, home to the University of Delaware, also sees device-related hiring driven by proximity to research partnerships. Smaller pockets of device manufacturing activity exist in New Castle County, which borders the broader Philadelphia-area life sciences corridor.
How do I find medical devices F-1 STEM OPT sponsorship jobs in Delaware?
Migrate Mate lets you filter specifically for medical devices roles with F-1 STEM OPT sponsorship history in Delaware, surfacing employers that have previously filed Labor Condition Applications for STEM-eligible positions. This is more targeted than general job searches because it focuses on verified sponsorship activity rather than self-reported labels. Filtering by SOC code for biomedical engineers and quality engineers within Delaware narrows results to roles most likely to qualify for your STEM OPT authorization.
What types of medical devices roles typically qualify for F-1 STEM OPT sponsorship?
Roles that qualify for STEM OPT typically carry a STEM-designated SOC code and require a directly related STEM degree. In medical devices, this commonly includes biomedical engineering, quality systems engineering, regulatory affairs (with an engineering or science degree), manufacturing process engineering, and research and development positions. O*NET classifies most of these under engineering or biological science occupation groups that appear on the official STEM OPT designated degree program list maintained by ICE.
Are there state-specific considerations for F-1 STEM OPT sponsorship in Delaware's medical devices industry?
Delaware's medical devices employers must comply with federal E-Verify requirements for STEM OPT, which your employer and Designated School Official handle jointly through a formal training plan. Delaware has no state-level immigration filing requirements beyond federal obligations, but the state's proximity to FDA district offices in Philadelphia can influence how quickly device companies build compliance infrastructure. Employers already operating under FDA quality system regulations tend to have streamlined HR processes for sponsoring STEM OPT candidates.