Software Architect - Medical Device
$200k - $220kCyberCoders
Software ArchitectSalary Range: $200,000 - $220,000 + full benefits & retirement plan Location: Burlington, MA area (Onsite, with consideration for hybrid flexibility) Industry: Medical Device DiagnosticsMust-Have Core SkillsMedical Device Expertise: Proven experience developing software under ISO 13485, IEC 62304, or 21 CFR Part 820.30 regulations.Education & Experience: BS with 15+ years of experience OR MS with 10-15+ years of software engineering experience.Hands-on & Architecture: Active proficiency in C++, Java, Angular, or Python, paired with deep expertise in distributed microservices architectures.Linux Systems: In-depth understanding of Linux OS internals (kernel, device drivers, filesystems) and tools like Yocto, CMake, and Docker.Leadership: Demonstrated track record mentoring technical team leads and driving platform-level design consistency.About the OpportunityJoin a global leader in specialized medical diagnostics operating in over 30 countries. This stable, family-owned organization employs over 7,000 professionals and focuses on developing highly customized medical assays and biomaterials that directly impact patient care and hospital efficiency.Position SummaryReporting to the Software Manager for Architecture and Platforms, you will own the software architecture across multiple product lines. You will bridge high-level product strategy with execution, establishing technical standards, mentoring engineering teams, and ensuring a secure, highly reliable software ecosystem.Key ResponsibilitiesArchitectural Ownership: Define and maintain the software architecture for core product lines to ensure long-term platform consistency.Team Leadership: Lead and align technical team leads and engineers with the product architecture vision.Execution & Scoping: Drive Work Breakdown Structures (WBS) and technical requirements alongside Product Owners and Functional Leads.Technical Quality: Conduct rigorous code/design reviews, develop proof-of-concepts, and write complex code to resolve high-priority platform challenges.Cross-Functional Collaboration: Harmonize development efforts across global R&D software teams, Scrum Masters, and Quality Test Engineering.Desired Premium Skills (A Plus)Experience with cybersecurity, threat modeling, or SE Linux.Experience within motor control domains or robotics job scheduling.Familiarity with Assembly, C, C#, or .NET frameworks.Minimal travel requirements (less than 5%).About the OpportunityStep into a high-impact leadership role with a global giant in specialized medical diagnostics. If you want your architectural decisions to directly improve hospital efficiency and patient care worldwide, this is your next career move.Position SummaryAs a Software Architect, you will own the technical blueprint for high-visibility software platforms. Reporting to the Software Manager for Architecture and Platforms, you will govern technology selection, architectural standards, and design practices across multiple product lines. You will bridge the gap between high-level product vision and hands-on execution, ensuring a reliable, high-quality software ecosystem.Key ResponsibilitiesArchitectural Ownership: Define and maintain the software architecture for key product lines to ensure platform consistency and scalability.Technical Leadership: Lead, mentor, and align technical team leads and software engineers with the long-term product vision.Project Scoping: Support requirements generation and drive product Work Breakdown Structures (WBS) alongside Product Owners and Functional Leadership.Hands-on Problem Solving: Perform code and design reviews, develop proof-of-concepts, and write complex code to resolve high-priority technical issues.Innovation & Research: Evaluate and integrate third-party technologies and industry trends to power next-generation product development.Global Collaboration: Harmonize development efforts across international R&D teams, Scrum Masters, and Quality Test Engineering.Desired Premium Skills (A Plus, Not Required)Experience in medical device software development (ISO 13485, IEC 62304, or 21 CFR Part 820.30).Knowledge of cybersecurity practices, including threat modeling and SE Linux.Familiarity with motor control domains or robotics job scheduling.Experience with Assembly, C, C#, or .NET frameworks.What Is on OfferCompetitive base salary ($200k - $220k) tailored to experience.Comprehensive medical, dental, and vision insurance packages.401(k) retirement plan with an employer match.Generous paid vacation, sick leave, and performance-based bonus eligibility.Exceptional work-life balance with minimal travel requirements (less than 5%).
- ...A medical device company in Bedford, NH, is seeking a Software Architect to oversee the design and development of medical device software. This role requires significant industry experience and proficiency in multiple programming languages. Responsibilities include developing...Medical deviceWork at office
- ...Description Position Overview Responsible for the high-level architecture and design of medical device software, ensuring alignment with system and software requirements. This “hands‑on” role requires you to be in our Bedford, NH office to collaborate with project managers...Medical deviceWork at office
- Merrimack Manufacturing is seeking a reliable 1st Shift Manufacturing Technician to assemble medical devices and document mechanical and electrical assemblies. The role requires self-sufficiency in assembly, testing, and documentation in a regulated environment. Schedule...Medical deviceMonday to FridayDay shift
- Merrimack Manufacturing is seeking a reliable 2nd Shift Manufacturing Technician to assemble medical devices with attention to detail in a structured environment. The role requires self-sufficiency in assembly, testing and documentation of mechanical and electrical assemblies...Medical deviceAfternoon shift
- DEKA Research and Development in Manchester, NH, seeks a qualified individual to assess complaints regarding medical devices. The role requires strong knowledge of FDA regulations and experience with complaint handling. Candidates should possess a biomedical engineering...Medical device
- DEKA Research & Development is seeking a Junior Product Complaints Engineer to join a dynamic Medical Device R&D environment in Manchester, NH. You will review complaints and perform evaluations, ensuring documentation aligns with FDA regulations and QMS requirements....Medical device
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- ...is seeking a Senior Mechanical Engineer to develop innovative medical devices in Southern New Hampshire. This requires being onsite 5... .... Work with multi-disciplinary team including electrical, software, industrial design, controls, and systems engineers, along with...Medical device
- ...Research & Development, located in Manchester, NH, is seeking a Verification & Validation Test Engineer to work in a dynamic medical device R&D environment. This is a high visibility role with a direct impact on the success of our projects. It will be a great opportunity...Medical device
$28 - $35 per hour
...BMET II Channel Services may serve as technical advisor to the medical and clinical staff in the safe operation and use of clinical equipment... ...(II) to maintain a complete and accurate inventory of medical devices, including trial and evaluation, rental, and loaner equipment...Medical deviceHourly payFull timeFor subcontractorRemote workWork from home- ...utilities and/or plant utilities, preferably in the biotechnology, medical device or pharmaceutical industry.Strong understanding of technical... ...good written communication skills.Proficiency with standard software applications, including MS Word, MS Excel, MS Project, MS...Medical deviceFull timeFor contractors
$145.31k - $196.6k
.... This includes providing disease information and education to medical professionals and all external customers involved in the care of... ...of sales experience within pharmaceutical, biotech or medical device industry or hospital sales experienceORAssociate degree and 6 years...Medical deviceFull timePrivate practiceWork at officeLocal areaRemote workFlexible hoursNight shift- ...Validation Engineer We are seeking a seasoned Validation Engineer with 10+ years of experience in medical device or regulated manufacturing environments. Candidates must have strong hands-on expertise in IQ/OQ/PQ protocol development and execution for both new and...Medical device
- ...development teams to deliver highly innovative devices that improve the lives of others. You... ...with a minimum of 5 years leading medical device product development teams solving... ...electromechanical products with embedded software Direct experience leading projects from...Medical device
- A leading medical device company in Manchester, NH is seeking a Regulatory Affairs Project Manager. The role involves defining and executing regulatory strategies for FDA approval of innovative life science devices, mentoring staff, and leading FDA interactions. Candidates...Medical device
- DEKA Research and Development is seeking a Regulatory Affairs Project Manager to lead regulatory strategy for medical device programs. You will define requirements, prepare submissions, and guide cross‑functional teams to approvals and clearances. You will interact with...Medical device
- Merrimack Manufacturing, a medical device manufacturer in Manchester, NH, is seeking a full-time Accounts Payable Specialist to join our finance team. The role focuses on timely processing of vendor invoices, 3-way matching, and related tasks in a fast-paced manufacturing...Medical deviceFull time
- Natus Medical is seeking a Territory Manager for BrainWatch in the Northeast. You will lead sales efforts to acquire new subscriptions... ...strong consultative selling approach, with 5+ years in medical device or healthcare tech sales, and the ability to navigate multi-stakeholder...Medical device
- ...ManagerDEKA Research & Development has an immediate opening for a Regulatory Affairs Project Manager to contribute to a dynamic, medical device research and development environment. The individual in this high visibility role will have a significant and direct impact on...Medical deviceWork experience placementImmediate start
- ...Senior Software Quality Assurance EngineerDEKA Research and Development, housed in Manchester, NH, is looking for a dynamic, results... ...Engineer to support the development of life-changing medical devices.How You Will Make An Impact As A Senior Software Quality Engineer...Medical deviceWork at office
- ...may be considered in lieu of degree. ~3–5 years of experience in Supplier Quality, Quality Engineering, or related role in medical device or regulated industry ~ Strong knowledge of ISO 13485 and medical device regulatory requirements ~ Experience with supplier...Medical deviceContract work
- ...seeking a Mechanical Drafter for a contract-to-perm role. You will be involved in preparing and releasing engineering drawings in a medical device environment. Candidates must have a minimum of 2 years of SolidWorks experience and strong attention to detail. This position...Medical devicePermanent employmentFull timeContract work
- ...technologies. DEKA R&D has an immediate opening for a Calibration Technician to work on the Quality team in a modern dynamic Medical Device Research and Development environment. This is a high visibility role with a significant impact on the schedules and success of...Medical deviceContract workWork at officeImmediate start
- ...COMPANY OVERVIEW: Merrimack Manufacturing is a medical device manufacturer located in the Manchester Millyard. We are a growing manufacturing company that will play a crucial part in bringing innovative and life changing products to life. POSITION OVERVIEW: Merrimack...Medical deviceWork at officeNight shift
- Company Overview Merrimack Manufacturing is a medical device manufacturer located in the Manchester Millyard. We are a growing manufacturing company that will play a crucial part in bringing innovative and life changing products to life. Position Overview We are currently...Medical deviceFull timeFlexible hours
- ...COMPANY OVERVIEW: Merrimack Manufacturing is a medical device manufacturer located in the Manchester Millyard. We are a growing manufacturing... ...authority ~ High proficiency utilizing project management software (i.e. MS Project) and continually refining systems to help...Medical device
- ...Senior Manufacturing Engineer As a Senior Manufacturing Engineer at DEKA, you'll play a critical role in transforming innovative medical device designs into scalable, high-quality, and regulatory-compliant manufacturing solutions. You'll work at the intersection of...Medical device
- ...Engineering, Life Sciences, or a related field ~3+ years of experience in a quality systems role in a regulated industry, ideally medical devices ~ Working knowledge of FDA QSR (21 CFR Part 820) and ISO 13485 ~ Proficiency with Microsoft Excel, Word, and Visio (or...Medical device
- ...Manufacturing, Six Sigma, or green manufacturing principles is a plus. Proficiency in CAD software; SolidWorks preferred. Familiarity with ERP systems is a plus. Experience in medical device manufacturing is highly desirable. Proven ability to set up manufacturing...Medical device
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