Staff Software Engineer, Medical Devices & Healthcare Integration

About Analog Devices

Analog Devices, Inc. (NASDAQ: ADI) is a global semiconductor leader that bridges the physical and digital worlds to enable breakthroughs at the Intelligent Edge. ADI combines analog, digital, AI, and software technologies into solutions that combat climate change, reliably connect humans and the world, and help drive advancements in automation and robotics, mobility, healthcare, energy and data centers. With revenue of more than $11 billion in FY25, ADI ensures today's innovators stay Ahead of What's Possible. Learn more at www.analog.com and on LinkedIn and X.

Software Engineer, Medical Devices & Healthcare Integration

A rapid research and development group within Analog Devices, Inc. is seeking a Software Engineer to develop next-generation medical devices, diagnostic platforms, and clinical laboratory systems.

This role requires hands-on experience developing software for laboratory or diagnostic equipment that integrates with LIS/LIMS systems. Candidates without this specific experience will not be considered.

The ideal candidate has experience taking connected medical or diagnostic products from development through verification, validation, and deployment in regulated healthcare environments. You will work closely with engineers, scientists, clinicians, and healthcare stakeholders to turn new concepts into production-ready technologies.

Key Responsibilities

• Design and develop software for medical devices, diagnostic instruments, laboratory equipment, and connected healthcare systems.
• Develop integrations between instruments and LIS/LIMS platforms, including bidirectional workflows for orders, specimens, instrument communication, and results.
• Implement healthcare interoperability standards such as HL7, FHIR, ASTM, and DICOM.
• Develop software for instrument control, sensor integration, data acquisition, analytics, APIs, and clinical or laboratory workflows.
• Collaborate with engineering, clinical, laboratory, and healthcare IT teams to define requirements and deploy solutions.
• Support regulated software development activities including requirements, risk analysis, design reviews, verification, validation, traceability, and change control.

Required Qualifications

• 5+ years of software development experience in medical devices, diagnostics, laboratory instrumentation, or related regulated healthcare products.
• Demonstrated experience developing software for laboratory or diagnostic equipment that communicates with LIS/LIMS systems.
• Hands-on experience with bidirectional LIS/LIMS integration, including workflows such as order ingestion, specimen management, instrument communication, and results transmission.
• Experience with healthcare interoperability protocols and standards such as HL7 v2.x, FHIR, ASTM, and/or DICOM.
• Strong Python development skills and experience with modern frameworks such as FastAPI, Pydantic, SQLModel, PyTorch, or comparable technologies.
• Experience with instrumentation software, device communications, embedded interfaces, or hardware/software integration.
• Experience developing software within FDA-regulated medical device processes, including software verification and validation.
• Working knowledge of relevant standards and quality processes such as IEC 62304, ISO 13485, ISO 14971, FDA Design Controls, and medical-device cybersecurity requirements.

Preferred Qualifications

• Experience integrating instruments with platforms such as Epic Beaker, Oracle Cerner, MEDITECH, Sunquest, SCC Soft, Orchard, Mirth/NextGen Connect, or similar laboratory systems.
• Experience developing commercial IVD products, laboratory automation, digital pathology, or diagnostic systems.
• Experience supporting FDA 510(k), PMA, CE Mark, or other regulatory submissions.
• Experience with embedded Linux, C/C++, Go, or Rust.
• Experience with machine learning applications in diagnostics, pathology, imaging, or laboratory analytics.
• Experience deploying products within hospitals, reference laboratories, academic medical centers, or healthcare networks.

Additional Requirements

• Willingness to live in Massachusetts and work onsite as required.
• Strong collaboration, problem-solving, and communication skills.
• Ability to work independently in a multidisciplinary R&D environment.

For positions requiring access to technical data, Analog Devices, Inc. may have to obtain export licensing approval from the U.S. Department of Commerce - Bureau of Industry and Security and/or the U.S. Department of State - Directorate of Defense Trade Controls. As such, applicants for this position – except US Citizens, US Permanent Residents, and protected individuals as defined by 8 U.S.C. 1324b(a)(3) – may have to go through an export licensing review process.

Analog Devices is an equal opportunity employer. We foster a culture where everyone has an opportunity to succeed regardless of their race, color, religion, age, ancestry, national origin, social or ethnic origin, sex, sexual orientation, gender, gender identity, gender expression, marital status, pregnancy, parental status, disability, medical condition, genetic information, military or veteran status, union membership, and political affiliation, or any other legally protected group.

EEO is the Law: Notice of Applicant Rights Under the Law.

• Actual wage offered may vary depending on work location, experience, education, training, external market data, internal pay equity, or other bona fide factors.

• This position qualifies for a discretionary performance-based bonus which is based on personal and company factors.

• This position includes medical, vision and dental coverage, 401k, paid vacation, holidays, and sick time, and other benefits.

From the posting on Analog Devices's job site. Read the original before you apply.