About the role#
As a Urology R&D Software Engineering Co-op, you will gain hands-on experience designing, developing, and testing software for next-generation medical devices. You will work within our Urology division on Class II and Class III devices, including advanced capital equipment and active implantable technologies. This role provides exposure to the full software development life cycle, from system architecture and requirements definition to implementation and testing. You will collaborate with cross-functional teams, including Research and Development, Quality, Manufacturing, Regulatory, and Clinical, to solve technical challenges and advance new products toward commercial launch.
What you'll do#
- Contribute to the architecture, development, and deployment of software and system solutions.
- Support efficient, maintainable software development processes, tools, and workflows.
- Participate in new product development activities to advance technologies toward regulatory approval.
- Evaluate technical challenges, analyze data, and recommend solutions.
- Prepare technical reports and documentation to communicate engineering findings.
- Assist in troubleshooting product and process challenges related to software design and manufacturing.
- Support the development and execution of test procedures.
- Assist in training technicians and operators in new processes.
- Contribute to new product concepts and submit innovative ideas.
- Collaborate with Process Development, Quality, Manufacturing, Regulatory, Clinical, and Marketing teams.
- Participate in engineering projects aligned with business needs and your technical interests.
What you'll need#
- Currently pursuing a bachelor's or graduate degree in software, electrical, systems, or biomedical engineering.
- Expected graduation date between Fall/Winter 2027 and Spring 2030.
- Eligibility to work in the U.S. without company sponsorship.
- Available for the full co-op duration from Jan. 11 through Aug. 6 or Aug. 13, 2027.
- Experience with safety-critical software development life cycles.
- Experience collaborating with project managers to plan activities and execute milestones.
- Familiarity with AI productivity tools like Microsoft 365 Copilot, ChatGPT, Claude Code, or GitHub Copilot.
- Professional experience using at least one programming language such as C, C++, C#, or Python.
- Familiarity with medical device risk assessment methodologies, including DFMEA and hazard analysis.
- Experience with source control, CI/CD, and requirements management tools like Git, Bitbucket, Jira, Jenkins, and Cockpit.
- Familiarity with medical device cybersecurity activities, including threat modeling, vulnerability assessments, and penetration testing.
Location & details#
- Locations: Maple Grove, Minnesota, or Marlborough, Massachusetts.
- Modality: Hybrid (requires being in the local office at least three to four days per week).
- Status: Paid, full-time co-op.
- Note: This role is deemed safety-sensitive and requires a prohibited substance test.
About Boston Scientific
Boston Scientific manufactures medical devices and technologies for patients globally. The company develops tools for diagnosing and treating conditions in areas such as cardiovascular, respiratory, and neurological health. It operates as a public company with over 54,000 employees. The headquarters is located in Marlborough, Massachusetts.
How to get in at Boston Scientific
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