Sr. Associate II, Software Engineering

Alcon; Bengaluru; On-site; INR 3,000,000 - 5,200,000; Full time

Benefits offered by this job

Relocation assistance

Job summary

Alcon in Bengaluru, India seeks a Senior Software Engineer specialized in C, C++, and C# for embedded software in ophthalmic devices. You will contribute across the software lifecycle, from requirements to testing, ensuring safety-critical compliance and documentation alignment with medical device standards.

The role emphasizes hands-on Windows development, multi-threaded architectures, and collaboration within an Agile environment, with relocation support where needed.

Qualifications

• 5+ years of software development experience in safety-critical environments.
• Experience with C, C++, C#, .NET applications.
• Hands-on Windows development and multi-threading experience.

Responsibilities

• Develop and maintain C, C++, C# applications using .NET.
• Ensure IEC 62304 and FDA-regulated SDLC compliance.
• Collaborate in Agile/Scrum to deliver high-quality software.
• Design, implement, and maintain automated unit tests and test frameworks.
• Produce software engineering documentation: requirements, architecture, design, tests.
• Participate in code reviews, risk assessments, and design discussions.
• Mentor junior engineers and contribute to process improvements.

Skills

C

C++

C#

NET

Windows

Multithreading

Git

English

Safety-critical

Medical devices

Education

Bachelor's degree in CS/Engineering

Tools

QNX RTOS

Photon GUI

Microsoft tech stack

Job description

About Alcon

At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers. We foster an inclusive culture and are looking for diverse, talented people to join Alcon.

Summary of Position

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

Alcon is an Equal Opportunity Employer

Alcon is an Equal Opportunity Employer and takes pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital status, disability, or any other reason.