Sr. Associate II, Software Engineering

Alcon Laboratories

Bengaluru

On-site

INR 1,800,000 - 3,200,000

Full time

5 days ago
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Benefits offered by this job

Relocation assistance

Job summary

Alcon Laboratories is seeking a Senior Software Engineer to develop embedded software for ophthalmic devices. You will work across the software lifecycle, from requirements to testing, focusing on safety-critical C, C++, and C# interfaces with .NET.

You will ensure compliance with IEC 62304 and FDA-regulated processes while collaborating in an Agile environment and mentoring junior engineers. This Bengaluru-based role includes relocation assistance.

Qualifications

  • 5+ years of work experience in software for medical devices.
  • Strong proficiency in C, C++, C#, and .NET development.
  • Hands-on Windows development experience and safety-critical systems exposure.
  • Experience with IEC 62304 and FDA-regulated software processes.

Responsibilities

  • Develop and maintain C, C++, C# applications using .NET.
  • Ensure compliance with IEC 62304 and FDA-regulated processes.
  • Collaborate in an Agile/Scrum environment to deliver high-quality software.
  • Design, implement, and maintain automated unit tests and test frameworks.
  • Document software architecture, requirements, design, and test protocols.
  • Participate in code reviews, risk assessments, and design discussions.
  • Mentor junior engineers and contribute to continuous improvement.

Skills

C
C++
C#
Multi-threading
Interprocess communication
Agile/Scrum
Safety-critical software

Education

University Degree in Computer Science, Engineering, or related discipline

Tools

Git
QNX RTOS
Photon GUI
.NET
Windows development

Job description

Job Summary

As a Senior Software Engineer C, C++, C#, hardware/software interfaces, you will be responsible for the development and documentation of complex software applications embedded in state-of-the-art ophthalmic surgical and medical devices. You will participate in all phases of the software lifecycle, including requirements, architecture, detailed design, implementation, and testing.

This role requires expertise in C, C++, C# development with .NET, strong knowledge of safety-critical systems, and compliance with medical device standards. In this position, you will also gain an in-depth understanding of the anatomy, physiology, and pathology of the eye.

Key Responsibilities
  • Develop and maintain C, C++, C# applications using .NET.
  • Ensure compliance with IEC 62304 and FDA-regulated medical device software development processes.
  • Collaborate in an Agile/Scrum environment to deliver high-quality software.
  • Design, implement, and maintain automated unit tests and test automation frameworks.
  • Author and maintain comprehensive software engineering documentation, including:
    • Requirements specifications
    • Software architecture documents
    • Detailed design descriptions
    • Test protocols and reports
  • Participate in code reviews, risk assessments, and design discussions to ensure safety and reliability.
  • Mentor junior engineers and contribute to continuous improvement initiatives.
Key Requirements / Minimum Qualifications
  • University Degree in Computer Science, Engineering, or related discipline with 5+ years of work experience.
  • 5-10 years of professional experience developing safety-critical software in the medical device industry.
  • Strong proficiency in C, C++, C#, .NET application development.
  • Hands-on Windows development experience.
  • Experience with multi-threading and interprocess communication.
  • Familiarity with software architecture and object-oriented design patterns.
  • Experience using Git for version control.
  • Excellent written and verbal English communication skills.
Preferred Qualifications
  • Additional experience with QNX RTOS, Photon GUI and Microsoft technology stacks.
  • Additional experience in developing and optimizing software algorithms for galvo control systems.
  • Development of medical device software in an FDA-regulated environment including knowledge of IEC 62304 and medical device software lifecycle processes.
  • Familiarity with hardware design constraints as applied to software interfaces.
  • Communication experience using TCP/IP.
  • Strong working knowledge of advanced design principles that facilitate maintainability, reuse, and clarity of design.
  • Demonstrated ability to independently research technical issues and generate creative/innovative solutions.

Work hours: 1 PM to 10 PM IST

Relocation assistance: Yes

Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.

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