Pharmavise Corporation
Senior Software Engineer Medical Device (Hybrid Waltham, MA) Contract
Pharmavise Corporation, Watertown, Massachusetts, us, 02472
Senior Software Engineer Medical Device (Hybrid Waltham, MA) Contract
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Senior Software Engineer Medical Device (Hybrid Waltham, MA) Contract
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Pharmavise Corporation Senior Software Engineer Medical Device (Hybrid Waltham, MA) Contract
1 week ago Be among the first 25 applicants Join to apply for the
Senior Software Engineer Medical Device (Hybrid Waltham, MA) Contract
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Pharmavise Corporation Get AI-powered advice on this job and more exclusive features. Our Fortune 500 Medical Device client has an exciting opportunity for a Principal Software Engineer.
Job Summary: We are looking for a Principal Software Engineer with strong software development experience in QT User Interface Software Development to join our exciting and fast-paced development team. The successful candidate will be involved in all aspects of the system's software, including Graphical User Interface development. They will also interface with other teams, such as systems engineering, hardware engineering and technicians from the field, to develop meaningful tools for the Opal Mapping System.
The Opal HDx Mapping System centers around a real-time virtual world of the human heart. As a physician probes the heart with a catheter, the system generates an accurate anatomical model of the chamber. High-performance rendering and algorithmic techniques are vital to creating a stunning view and providing the physician with instant feedback.
Our technology includes C++ (C++11 or newer), Qt (Qt Widgets or Qt Quick/QML), Linux.
Key Responsibilities: The Principal Software Engineer will have a key role in the development of communication protocols for cutting edge medical applications in the field of Cardiac arrhythmia diagnosis and treatment. The responsibilities will include: Provide technical leadership to the team in software architecture and best in class software development methodologies and practices. Architect, design, develop and release innovative high performance medical device software. Solve difficult problems, improve state of the art, and achieve engineering excellence. Collaborate across disciplines effectively (HW, Systems, Test, Quality, Regulatory) to focus and maximize end-to-end solution value and quality Participates in preclinical system experiments in the lab, with physicians, and 3rd parties
Quality Systems Duties and Responsibilities: Build Quality into all aspects of their work by maintaining compliance to all quality requirements, e.g. Requirements, Design, and User Story documentation and review.
Qualifications: BS/MS in Computer Science or equivalent experience, with a strong software development background. 8+ years relevant Experience C++ development and debugging Experience QT GUI Experience, including Qt Widgets and/or Qt Quick/QML Experience with Object Oriented programming principles Excellent analytical and problem-solving skills Ability to contribute to multiple projects in parallel Implements, tests, troubleshoots, and debugs source code for complex software applications Follow the full design life cycle process including driving efforts in requirements specification, design activities, planning, code reviews and creating corresponding artifacts. Participate in the development of technical documentation, including design specifications, test plans, and user manuals. Promote a collaborative environment and pragmatic engineering decision-making. Identify and implement continuous improvements to work processes and tools. Support field clinical staff on use of medical software and troubleshooting of issues.
Preferred Qualifications: Experience with developing on the Linux platform Experience with scrum framework Good written and verbal communication skills. General report writing/documentation experience Experience with medical device standards including IEC 62304, 60601, ISO 14971, 13485 Experience with software configuration management tools for source code control (Git), issue tracking (Jira), requirements management (JAMA) A good learner who can master complex software and quickly adapt to new tools and technologies. Experience mentoring lower-level engineers
Other Details: Schedule: 09:00 AM - 05:00 PM EDT Work Setup: Hybrid in Waltham, MA (minimum of 3 days per week onsite) May require limited travel. Contract Length: 12 Months (09/22/2025 - 09/21/2026)
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Mid-Senior level Employment type
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Information Technology Industries
Medical Equipment Manufacturing Referrals increase your chances of interviewing at Pharmavise Corporation by 2x Sign in to set job alerts for Senior Software Engineer roles.
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Join to apply for the
Senior Software Engineer Medical Device (Hybrid Waltham, MA) Contract
role at
Pharmavise Corporation Senior Software Engineer Medical Device (Hybrid Waltham, MA) Contract
1 week ago Be among the first 25 applicants Join to apply for the
Senior Software Engineer Medical Device (Hybrid Waltham, MA) Contract
role at
Pharmavise Corporation Get AI-powered advice on this job and more exclusive features. Our Fortune 500 Medical Device client has an exciting opportunity for a Principal Software Engineer.
Job Summary: We are looking for a Principal Software Engineer with strong software development experience in QT User Interface Software Development to join our exciting and fast-paced development team. The successful candidate will be involved in all aspects of the system's software, including Graphical User Interface development. They will also interface with other teams, such as systems engineering, hardware engineering and technicians from the field, to develop meaningful tools for the Opal Mapping System.
The Opal HDx Mapping System centers around a real-time virtual world of the human heart. As a physician probes the heart with a catheter, the system generates an accurate anatomical model of the chamber. High-performance rendering and algorithmic techniques are vital to creating a stunning view and providing the physician with instant feedback.
Our technology includes C++ (C++11 or newer), Qt (Qt Widgets or Qt Quick/QML), Linux.
Key Responsibilities: The Principal Software Engineer will have a key role in the development of communication protocols for cutting edge medical applications in the field of Cardiac arrhythmia diagnosis and treatment. The responsibilities will include: Provide technical leadership to the team in software architecture and best in class software development methodologies and practices. Architect, design, develop and release innovative high performance medical device software. Solve difficult problems, improve state of the art, and achieve engineering excellence. Collaborate across disciplines effectively (HW, Systems, Test, Quality, Regulatory) to focus and maximize end-to-end solution value and quality Participates in preclinical system experiments in the lab, with physicians, and 3rd parties
Quality Systems Duties and Responsibilities: Build Quality into all aspects of their work by maintaining compliance to all quality requirements, e.g. Requirements, Design, and User Story documentation and review.
Qualifications: BS/MS in Computer Science or equivalent experience, with a strong software development background. 8+ years relevant Experience C++ development and debugging Experience QT GUI Experience, including Qt Widgets and/or Qt Quick/QML Experience with Object Oriented programming principles Excellent analytical and problem-solving skills Ability to contribute to multiple projects in parallel Implements, tests, troubleshoots, and debugs source code for complex software applications Follow the full design life cycle process including driving efforts in requirements specification, design activities, planning, code reviews and creating corresponding artifacts. Participate in the development of technical documentation, including design specifications, test plans, and user manuals. Promote a collaborative environment and pragmatic engineering decision-making. Identify and implement continuous improvements to work processes and tools. Support field clinical staff on use of medical software and troubleshooting of issues.
Preferred Qualifications: Experience with developing on the Linux platform Experience with scrum framework Good written and verbal communication skills. General report writing/documentation experience Experience with medical device standards including IEC 62304, 60601, ISO 14971, 13485 Experience with software configuration management tools for source code control (Git), issue tracking (Jira), requirements management (JAMA) A good learner who can master complex software and quickly adapt to new tools and technologies. Experience mentoring lower-level engineers
Other Details: Schedule: 09:00 AM - 05:00 PM EDT Work Setup: Hybrid in Waltham, MA (minimum of 3 days per week onsite) May require limited travel. Contract Length: 12 Months (09/22/2025 - 09/21/2026)
Seniority level
Seniority level
Mid-Senior level Employment type
Employment type
Contract Job function
Job function
Information Technology Industries
Medical Equipment Manufacturing Referrals increase your chances of interviewing at Pharmavise Corporation by 2x Sign in to set job alerts for Senior Software Engineer roles.
Boston, MA $180,000.00-$220,000.00 6 months ago Boston, MA $250,000.00-$300,000.00 3 weeks ago Senior Software Engineer, Assistant Vice President
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