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Biomedical Software Engineer Jobs in Boston, MA (NOW HIRING)

From military defense and space exploration to biomedical engineering, lives often depend on the ... The Software Engineer (SMTS) develops high performance solutions for resource constrained targets.

From military defense and space exploration to biomedical engineering, lives often depend on the ... The Software Engineer (SMTS) develops high performance solutions for resource constrained targets.

From military defense and space exploration to biomedical engineering, lives often depend on the ... The Software Engineer (SMTS) develops high performance solutions for resource constrained targets.

From military defense and space exploration to biomedical engineering, lives often depend on the ... The Software Engineer (SMTS) develops high performance solutions for resource constrained targets.

From military defense and space exploration to biomedical engineering, lives often depend on the ... The Principal Embedded Software Engineer develops high performance solutions for resource ...

Sr. Systems Engineer

Billerica, MA · On-site

$111K - $151K/yr

S. in engineering discipline (e.g., Electrical, Mechanical, Biomedical, Software). M.S. preferred. * Experience: 7+ years' experience in medical device product development, including FDA regulated ...

From military defense and space exploration to biomedical engineering, lives often depend on the ... The Principal Embedded Software Engineer develops high performance solutions for resource ...

From military defense and space exploration to biomedical engineering, lives often depend on the ... Draper is seeking a senior embedded-software professional to lead the development of high ...

From military defense and space exploration to biomedical engineering, lives often depend on the ... The Senior Engineer will own the endtoend software lifecycle-from requirements analysis and ...

Sr. Systems Engineer

Billerica, MA · On-site

$120K - $155K/yr

S. in engineering discipline (e.g., Electrical, Mechanical, Biomedical, Software). M.S. preferred. * Experience: 7+ years' experience in medical device product development, including FDA regulated ...

Showing results 41-60

Biomedical Software Engineer information

See Boston, MA salary details

$69K

$160.3K

$223.3K

How much do biomedical software engineer jobs pay per year?

As of Aug 14, 2026, the average yearly pay for biomedical software engineer in Boston, MA is $160,270.00, according to ZipRecruiter salary data. Most workers in this role earn between $130,400.00 and $187,900.00 per year, depending on experience, location, and employer.

What does a biomedical software engineer do?

Biomedical Software Engineers often work on designing, developing, and maintaining software used in medical devices, clinical diagnostics, or healthcare information systems. Typical responsibilities include coding new features, troubleshooting and resolving software issues, ensuring compliance with medical standards, and participating in quality assurance testing. You may also collaborate closely with clinicians, researchers, and regulatory specialists to align technological solutions with user needs and safety requirements. These projects frequently involve iterative development and rigorous validation to ensure reliability in real-world medical settings.

What is a biomedical software engineer?

A Biomedical Software Engineer develops software solutions for medical and healthcare applications, including medical devices, diagnostic tools, and research simulations. They combine biomedical knowledge with software development skills to create and maintain systems that improve patient care, enhance medical research, and ensure regulatory compliance. Their work often involves programming, data analysis, and collaboration with healthcare professionals and researchers.

What skills and qualifications are needed to be a biomedical software engineer?

To thrive as a Biomedical Software Engineer, you need a strong background in computer science, biomedical engineering, and software development—often supported by a bachelor's or master's degree in a related field. Proficiency with programming languages such as Python, C++, or Java, familiarity with medical imaging tools, and experience working with healthcare interoperability standards like HL7 or DICOM are typically required. Effective communication, teamwork, and problem-solving skills are crucial for collaborating with cross-functional teams and understanding user requirements. These competencies ensure that biomedical software solutions are safe, compliant, and meet the complex needs of healthcare environments.

Infographic showing various Biomedical Software Engineer job openings in Boston, MA as of August 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 90% In-person, and 10% Hybrid job distribution, with an average salary of $160,270 per year, or $77.1 per hour.

Senior Design Quality Engineer Medical Device W2 preffered

PDDN INC.

Andover, MA • Hybrid

$89K - $121K/yr

Contractor

Posted 8 days ago


Job description

Job Description

Role name: Senior Design Quality Engineer
Work Location: Andover, MA
Start date: Immediate availability
Job Type: Contract (C2C/W2)
Interview: Phone/Video
Role and responsibilities:
Grade: C2=> 10-12 years
Location: Andover, MA/Remote
Working from client office: Yes (Hybrid 3 days per week).

Qualifications:
o Bachelor's degree in Engineering (Biomedical, Software, Systems) or a related technical discipline
o Advanced degree (Master's) in Engineering, Quality, or Regulatory Affairs preferred
o Relevant certifications (e.g., ASQ CQE, CSQE, Six Sigma Green/Black Belt) are a plus

Job Description
As a Senior Design Quality Engineer (DQE) for our medical device manufacturer client in the Greater Boston region, you will be responsible for ensuring endtoend design quality and compliance across the product development lifecycle for Class II/III medical devices, including software-driven and active implantable products. Working directly with cross-functional teams, you will drive adherence to design controls, risk management, and SDLC best practices from concept through commercialization and postmarket activities.

Key Responsibilities
In this role you will play a key role in:
Serving as the quality lead on product development teams, ensuring compliance with design controls across all lifecycle phases (planning, inputs/outputs, verification, validation, transfer, and change management)
Establishing and maintaining DHF, DMR, and DHR, ensuring complete traceability from user needs through verification and validation evidence
Leading and maintaining risk management activities (hazard analysis, FMEA, risk files) and ensuring integration of risk controls into design and validation activities
Providing quality oversight of software SDLC activities, ensuring compliance with applicable standards (e.g., IEC 62304) and integration with system-level risk management
Reviewing and approving design, software, and validation deliverables to ensure completeness, consistency, and audit readiness
Supporting verification, validation, and design transfer activities, ensuring alignment between design outputs and production processes
Leading or supporting CAPA, nonconformance investigations, and root cause analysis to drive continuous improvement
Supporting internal and external audits (FDA, Notified Body, ISO), and contributing to regulatory submissions (e.g., IDE, PMA, EU MDR)

Required Skills
10+ years of experience in Quality Engineering supporting regulated medical device development (Class II/III preferred)
Strong hands-on experience with design controls, DHF management, and traceability in regulated environments
Working knowledge of applicable standards and regulations (e.g., 21 CFR 820, ISO 13485, ISO 14971, IEC 62304)
Experience supporting software quality within the SDLC and understanding of software risk management principles
Proven experience with risk management tools (e.g., FMEA, hazard analysis) and integration into product development
Experience supporting audits and regulatory submissions, with the ability to defend design and quality documentation
Strong analytical, documentation, and communication skills with ability to work effectively across cross-functional teams
Experience with quality systems, eQMS/PLM tools, and defect/CAPA management processes

Additional Information

All your information will be kept confidential according to EEO guidelines.