Principal Software Quality Engineer - Medical Device #2949- Marlborough, MA
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Principal Software Quality Engineer - Medical Device #2949- Marlborough, MA
Location
Marlborough, MA, Marlborough, MA, 01752, USA
Experience
Senior
Posted
Jul 14, 2026
Apply by
August 13, 2026
Applicants
0
Early applicantEasy applyFull-timeWork from Office
Job Description
## Description
About ECI ECI’s mission is to be the global leader of professional consulting services for the life sciences industry. Our clients lean on our diverse perspectives and decades of expertise to tackle their toughest challenges, and we take pride in providing them transformative solutions with distinctive, sustainable and long-term value. ECI boasts a proven track record of providing full product life cycle consulting on a variety of challenging and exciting projects. Our collaborative culture, welcoming team and flexible employment & benefit options allow us to maintain strong relationships with the most talented individuals in the life sciences industry.
About the RoleThis is an exciting opportunity for a software focused Principal Software Quality Engineer supporting a cross-functional team on development and maintenance of Implantable and external devices and software. The role will apply the directives of design controls supporting the software development lifecycle (SDLC), software verification and validation (V&V), risk management, product development, run the business, and regulatory and standards compliance. This role is an onsite position in Marlborough, MA.
What You'll Do
- Participates in the implementation of new product software, including risk management (per ISO 14971), hazard analysis, software FMEAs, security risk analysis, software design V&V.
- Applies software application development procedures and provides support to demonstrate compliance through technical documentation generation.
- Participates in cross functional team meetings, software bug triage meetings to discuss, investigate and appropriately disposition internal software bugs and software field issues.
- Applies sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues (i.e. software bugs).
- Works within a cross-functional team to identify and implement effective controls and support product development from concept through commercialization.
- Updates and maintains software risk management tools (i.e. Hazard Analysis, FMEAs).
- Participates in Cybersecurity related discussions and assists supporting activities including Security Risk Analysis.
- Leads and participates in software and electronic design reviews, design transfers, and in all aspects of the Design Control process for the PCI Guidance products.
- Acts as an effective leader or team member in supporting quality disciplines, decisions, and practices.
- Assists in the design and development of software test cases and inspection procedures.
- Supports regulatory submissions to notified bodies.
- Demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.
What We Look For
- Bachelor’s degree in mechanical or biomedical engineering or related technical discipline.
- Demonstrated experience working with implantable medical devices, including development, testing, validation, or product lifecycle support.
- Demonstrated experience in firmware and software engineering.
- Experience with software validation, including test planning, protocol execution, defect identification, documentation, and verification of system performance against requirements.
- Experience with Issue Tracking Tools and requirements / test management tools.
- Understanding of software configuration management (version control, Microsoft office tools)
- Adaptable and effective collaborator in a team environment and in self-directed work
- Strong communication skills (verbal & written)
- Demonstrated use of Quality tools/methodologies
- Strong knowledge of Quality System Regulation (QSR), Risk Management standards and software standards (IEC 60601)
ECI is an equal opportunity employer.All qualified applicants will receive consideration for employment at ECI without regard to race; creed; color; religion; national origin; sex; age; disability; sexual orientation; gender identity or expression; genetic predisposition or carrier status; veteran, marital, or citizenship status; or any other status protected by law. At the time of this posting, all candidates must be authorized to work in the U.S. without the need for employment-based visa sponsorship now or in the future. At the time of this posting, ECI will not sponsor applicants for U.S. work visa status for this opportunity.
Key Responsibilities
- Implement new product software including risk management, hazard analysis, and software FMEAs.
- Apply software application development procedures to demonstrate compliance through technical documentation.
- Participate in cross-functional team meetings and software bug triage to resolve internal and field issues.
- Identify and resolve quality issues using systematic problem-solving methodologies.
- Support product development from concept through commercialization within a cross-functional team.
- Update and maintain software risk management tools such as Hazard Analysis and FMEAs.
- Participate in cybersecurity discussions and support security risk analysis activities.
- Lead and participate in software and electronic design reviews, design transfers, and design control processes.
- Assist in the design and development of software test cases and inspection procedures.
- Support regulatory submissions to notified bodies.
- Maintain compliance with Quality Policy and documented quality processes to ensure patient safety.
Requirements
- Bachelor's degree in mechanical or biomedical engineering or related technical discipline
Skills Required
Software ValidationTest PlanningProtocol ExecutionDefect IdentificationRequirements ManagementTest ManagementIssue Tracking ToolsSoftware Configuration ManagementVersion ControlMicrosoft OfficeQuality System Regulation (QSR)Risk Management StandardsIEC 60601Firmware EngineeringSoftware EngineeringMedical Device DevelopmentCommunicationCollaborationProblem SolvingAdaptabilitySelf-direction
Benefits
- Flexible employment options
- Competitive salary
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