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Medical Device Software Engineer Jobs in Washington

Alarm.com

Principal Software Engineer

Tysons Corner, VA

$135K - $182K/yr

Alarm.com combines the product breadth and technical scale of a mature connected-device platform ... The package includes medical plans with company subsidies, a Health Savings Account (HSA) with a ...

Maverc Technologies

Software Engineer

Laurel, MD · On-site

Experience with Linux and Windows internals and device driver development * Experience with embedded software development * Experience leading engineering teams from concept through operations and ...

REDLattice

Software Engineer

Chantilly, VA

Software Engineer Location: Northern Virginia (multiple locations) At REDLattice, we are a global ... Exposure to software development frameworks, mobile application tooling, or embedded device ...

REDLattice

Software Engineer

Chantilly, VA

Software Engineer Location: Northern Virginia (multiple locations) At REDLattice, we are a global ... Exposure to software development frameworks, mobile application tooling, or embedded device ...

REDLattice

Software Engineer

Chantilly, VA · On-site

Software Engineer Location: Northern Virginia (multiple locations) At REDLattice, we are a global ... Exposure to software development frameworks, mobile application tooling, or embedded device ...

REDLattice

Software Engineer

Chantilly, VA

Software Engineer Location: Northern Virginia (multiple locations) At REDLattice, we are a global ... Exposure to software development frameworks, mobile application tooling, or embedded device ...

Fusion Innovation

Senior Software Engineer

Reston, VA

$127K - $168K/yr

This role will also lead technical engagement with peripheral vendors, device middleware providers ... Partner with Software Architecture, Platform Engineering, Security, Field Engineering, Operations ...

NTT America

IoT / Edge Software Engineer

Bethesda, MD · Remote

$68K - $141K/yr

Develop and maintain secure device authentication, data encryption, and remote firmware update ... This position is eligible for company benefits including medical, dental, and vision insurance with ...

Navstar

Software Engineer

Annapolis Junction, MD · On-site +1

$150K - $210K/yr

... device development, and cryptographic/secure frameworks. Deep, hands-on Java experience is ... Comprehensive medical, dental, and vision plans. * Retirement Plan: 401(k) with company match.

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All JobsMedical Device Software Engineer JobsMedical Device Software Engineer Jobs in Washington

Medical Device Software Engineer information

See Washington salary details

$71.9K

$167.1K

$232.7K

How much do medical device software engineer jobs pay per year?

As of Jun 17, 2026, the average yearly pay for medical device software engineer in Washington is $167,085.00, according to ZipRecruiter salary data. Most workers in this role earn between $135,900.00 and $195,900.00 per year, depending on experience, location, and employer.

Who is eligible for Medi-Cal?

Medi-Cal is California's Medicaid program, providing health coverage to low-income individuals and families, including pregnant women, seniors, persons with disabilities, and those meeting income and asset requirements. Eligibility depends on income level, household size, and specific circumstances, and applicants often need to provide proof of income and residency. Medical device software engineers should verify their eligibility if seeking coverage for health-related needs or benefits related to employment.

What are the key skills and qualifications needed to thrive in the Medical Device Software Engineer position, and why are they important?

To thrive as a Medical Device Software Engineer, you need a solid background in software development, embedded systems, and biomedical engineering, often supported by a degree in computer science, electrical engineering, or a related field. Experience with programming languages like C/C++, knowledge of real-time operating systems, and familiarity with medical device regulatory standards such as IEC 62304 are typically required. Strong problem-solving skills, attention to detail, and effective communication are essential soft skills for this position. These skills ensure high-quality, compliant software that contributes to safe and reliable medical devices, which are critical for patient health.

What is a Medical Device Software Engineer job?

A Medical Device Software Engineer is responsible for designing, developing, testing, and maintaining software used in medical devices. They ensure compliance with regulatory standards like FDA and IEC 62304 while working on embedded systems, user interfaces, or cloud-based healthcare applications. Their role involves collaborating with cross-functional teams, including hardware engineers and regulatory specialists, to ensure patient safety and product effectiveness.

What does medical mean?

In the context of a Medical Device Software Engineer, 'medical' refers to products, devices, or software used for healthcare purposes, such as diagnosis, treatment, or monitoring of patients. These products are regulated to ensure safety and effectiveness and often require compliance with standards like FDA or ISO. The role involves developing software that meets strict quality and safety requirements specific to healthcare environments.

Is Medi-Cal the same as Medicaid?

Medical Device Software Engineers should understand that Medi-Cal and Medicaid are related but not identical; Medi-Cal is California's Medicaid program, which provides health coverage to low-income residents, while Medicaid is a federal and state program serving similar purposes across the U.S. Differences may include specific benefits, eligibility criteria, and administration. Knowledge of healthcare policies can be important when developing compliant medical software for different regions.

What are some typical daily responsibilities of a Medical Device Software Engineer?

Medical Device Software Engineers typically spend their days designing, coding, and testing software for medical devices in compliance with health regulations. They collaborate closely with hardware engineers, quality assurance teams, and regulatory specialists to ensure that the software integrates seamlessly with device hardware and meets performance and safety standards. Documenting development processes, participating in code reviews, and addressing feedback from cross-functional teams are also common aspects of the role. This position often requires troubleshooting issues in both simulated and real clinical environments to ensure the reliability and safety of the device.

What's the difference between Medicare and Medi-Cal?

Medicare is a federal health insurance program primarily for people aged 65 and older or with certain disabilities, while Medi-Cal is California's Medicaid program providing free or low-cost health coverage for low-income individuals. As a Medical Device Software Engineer, understanding these programs can be relevant when designing compliant healthcare software and ensuring accessibility for diverse patient populations.
What are the most commonly searched types of Medical Device Software Engineer jobs in Washington? The most popular types of Medical Device Software Engineer jobs in Washington are:
What are popular job titles related to Medical Device Software Engineer jobs in Washington? For Medical Device Software Engineer jobs in Washington, the most frequently searched job titles are:
What job categories do people searching Medical Device Software Engineer jobs in Washington look for? The top searched job categories for Medical Device Software Engineer jobs in Washington are:
What cities in Washington are hiring for Medical Device Software Engineer jobs? Cities in Washington with the most Medical Device Software Engineer job openings:
Medical Device Software Engineer jobs near you

Medical Device QMS Auditor

The British Standards Institution (BSI)

Reston, VA • On-site

$98K - $123K/yr

Full-time

Medical, Dental, Life, Retirement, PTO

Posted 27 days ago

Job description

We exist to create positive change for people and the planet. Join us and make a difference too!
Job Title: Medical Device QMS Auditor
Location: Candidates must reside in one of the following states: IL, MN, WI, IN, NJ, MA, PA, OH.
BSI (British Standards Institution) is the global business standards company that equips businesses with the solutions to turn standards of best practice into habits of excellence.
Our Medical Devices (or Regulatory Services) team ensures patient safety while supporting timely market access for our clients' medical device products globally. BSI is an accredited ISO 13485 Certification Body recognized in many global markets.
This is a travel based position with extensive travel to medical device manufacutering sites. Candidate must be comfortable with overnight travel of 13-15 days out of every month.
Essential Responsibilities
  • Analyze and assess quality management systems with emphasis on design controls, manufacturing controls, production processes, process validation, verification/validation, and testing activities, ensuring compliance with ISO 13485, CE Marking, and MDSAP schemes.
  • Assess manufacturing processes including production controls, process validation, risk management, supplier controls, and design transfer activities.
  • Prepare assessment reports and communicate findings to clients, providing clear direction for corrective actions where appropriate.
  • Recommend the issue, re-issue, or withdrawal of certificates in accordance with BSI policies and procedures.
  • Lead assessment teams, ensuring quality of service and effective working relationships with clients and team members.

Education & Technical Qualifications
  • Technical degree (Bachelor's, or higher) in Engineering, Science, or a related technical discipline required. Relevant fields include Biomedical, Mechanical, Electrical, or Chemical Engineering; Materials Science; Biology; Microbiology; Chemistry; or related technical fields applicable to medical devices, SaMDs, or IVDs.
  • Minimum of 4 years' experience in the medical device, SaMD, or IVD fields with direct, hands-on involvement in designing, manufacturing, validating, inspecting, testing, or clinically evaluating devices. Candidates must have personally worked with devices, specifications, or code, indicate the types and classifications of devices, and demonstrate their level of involvement on their CV. Regulatory or audit experience only is insufficient.
  • Detailed hands-on experience with design and manufacturing/production controls, including process validation (IQ/OQ/PQ), risk management, supplier controls, CAPA, nonconforming product management, and change control.
  • Knowledge of regulatory requirements and quality management standards including ISO 13485, MDSAP, FDA QSR (21 CFR 820), and EU MDR/IVDR are a plus

Core Competencies
  • Strong verbal and written communication skills, and attention to detail.
  • Ability to work under pressure and meet deadlines.
  • Self-motivated, flexible, and excellent time management/planning skills.
  • Willingness to travel extensively.
  • Enthusiastic, committed team player.
  • Business development and public speaking skills are considered advantageous.

Preferred Qualifications
  • Experience with process validation, equipment qualification, and manufacturing process development.
  • Experience in design and development activities, including design controls and design transfer.
  • Hands-on experience with software-controlled medical devices, SaMD, or automated manufacturing systems.
  • Experience auditing or assessing quality management systems compliant with ISO 13485, CE Marking, and MDSAP.
  • Experience with risk management (ISO 14971), sterile medical devices, aseptic processing, or cleanroom manufacturing.
  • Experience leading hands-on teams in manufacturing, testing, or validation.
  • Lead Auditor certification (ISO 13485, MDSAP, or equivalent) preferred.
  • Previous experience working for a Notified Body, Regulatory Body, or Certification Body preferred.
  • Advanced degree (MS, PhD) in engineering, science, or related technical discipline preferred.

The salary for this position can range from $98,100 to $123,860 annually; actual compensation is based on various factors, including but not limited to, the candidate's competencies, level of experience, education, location, divisional budget and internal peer compensation comparisons. BSI offers a competitive salary, group-sponsored health and dental, short-term and long-term disability, a company-matched 401k plan, company paid life insurance, 11 paid holidays and 4 weeks paid time off.
#LI-REMOTE
#LI-MS1
About Us
BSI is a business improvement and standards company and for over a century BSI has been recognized for having a positive impact on organizations and society, building trust and enhancing lives.
Today BSI partners with more than 77,500 clients in 195 countries and engages with a 15,000 strong global community of experts, industry and consumer groups, organizations and governments.
Utilizing its extensive expertise in key industry sectors - including automotive, aerospace, built environment, food and retail, and healthcare - BSI delivers on its purpose by helping its clients fulfil theirs.
Living by our core values of Client-Centricity, Agility, and Collaboration, BSI provides organizations with the confidence to grow by partnering with them to tackle society's critical issues - from climate change to building trust in digital transformation and everything in between - to accelerate progress towards a better society and a sustainable world.
BSI is an Equal Opportunity Employer dedicated to fostering a diverse and inclusive workplace.

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