Executive - Finance/Accounts

Minimum Required Experience : 12 years

Full Time

• *Skills**
• ---------

C\+\+

Software Architecture

QT

• *Description**
• --------------

Architect (C\+\+ with QT experience)\\

• *JD for Software Architect**

• *Experience 12–18 years**

• *Job Summary**

We’re seeking a seasoned Software Architect to design and govern the architecture for our medical device software stack. You’ll own the end\-to\-end architecture for C\+\+ core, Qt\-based UI, and device integration, ensuring safety, reliability, performance, and regulatory compliance in a healthcare environment.

• Define and drive the software architecture for C\+\+ core modules, Qt UI, and device interfaces.
• Translate clinical, regulatory, and product requirements into scalable, maintainable architecture and roadmaps.
• Establish design patterns, componentization, interfaces, and data models; govern architectural decisions and trade\-offs.
• Lead architectural reviews, ensure traceability to requirements, risk management, and safety\-related design activities.
• Ensure compliance with medical device regulations (e.g., ISO 13485, IEC 60601\-1, MDR/IVDR per region) and software lifecycle processes.
• Oversee safety, reliability, performance, cybersecurity, and fail\-safe behavior across the stack.
• Drive architecture for hardware\-software integration, drivers, middleware, real\-time constraints, and platform portability.
• Mentor software engineers and ensure effective code quality, reviews, and design documentation.
• Collaborate with UX/UI, QA, regulatory, hardware, and clinical teams to align architecture with user needs and validation plans.
• Define and maintain architecture artifacts: high\-level designs, component diagrams, interfaces, non\-functional requirements (NFRs), and API specs.
• Manage technical risk registers and mitigation plans; propose reuse strategies and platformization where feasible.

• *Required Qualifications**

• Bachelor’s or Master’s degree in Computer Science, Software Engineering, or related field.
• 8\+ years of professional software engineering experience in C\+\+ with strong object\-oriented and design\-pattern skills.
• 5\+ years in software architecture/leadership roles, preferably in medical device or regulated healthcare environments.
• Proven experience with Qt (widgets or QML) for complex, user\-centric desktop or embedded UI.
• Deep understanding of cross\-platform development, performance optimization, memory management, and real\-time considerations.
• Familiarity with hardware/firmware integration, device drivers, and IPC mechanisms.
• Solid knowledge of software development life cycle in regulated environments (requirements, design, implementation, verification, validation, change control).
• Experience with risk management processes (ISO 14971\) and software safety concepts.
• Strong communication and collaboration skills; proven ability to influence across disciplines.

• *Nice\-to\-Haves**

• Experience with embedded Linux, real\-time OS, or bare\-metal environments.
• Knowledge of cybersecurity standards and secure\-by\-design practices for medical devices.
• Experience with formal methods or model\-based design (UML, SysML, architecture frameworks).
• Fluency in additional languages used in healthcare (e.g., German, French) or global regulatory knowledge.
• Prior role in a compliance/audit context and successful regulatory submissions.

• *Technical Skills**

• C\+\+ (C\+\+11/14/17/20\), modern idioms, templates, RAII, STL, move semantics.
• Qt framework: widgets, signals/slots, QML, model\-view patterns, MVC/MVVM.
• Software architecture styles: layered, component\-based, event\-driven, service\-oriented.
• APIs, SDKs, middleware, and hardware abstraction layers.
• Architecture modeling: UML/SysML, architecture decision records (ADRs).
• Version control, CI/CD, test automation, and code quality tooling.
• Knowledge of standards: IEC 62304, ISO 62366 (use/error), ISO 14971, ISO 13485\.

• *Responsibilities (Regulatory and Quality)**

• Ensure design documentation supports regulatory submissions and audits.
• Maintain requirements traceability and evidence for verification/validation.
• Collaborate with cybersecurity, safety, and quality teams to meet regulatory expectations.