Associate II, Software Engineering
Alcon (company site, opens in a new tab)5+ yrsBengaluruOn-siteDirect career pageEst. 10–18 LPA
Posted 15h ago
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Job description
Structured overview of role & requirements
About This Role
- Plan and coordinate software documentation updates and ensure compliance with regulatory and procedural requirements.
- Collaborate with on-shore and off-shore Software Verification and Validation teams to support testing and related documentation updates.
- Maintain electronic documentation repositories (DHF and TFS) and support audit and compliance activities related to software development.
Minimum Requirements
- Bachelor’s degree in Computer Science, Software Development, MIS, BIS, or related field with 2 years of experience, or 5 years of relevant experience.
- Experience with document management systems (preferred: PLM Windchill) and tools like Microsoft Visual Studio, Azure DevOps, or other IDE tools.
- Some knowledge of ISO 14971, ISO 13485 (or US 21 CFR 820.30), and Software Development Lifecycle Management (SDLC).
- Work hours: 1 PM to 10 PM IST; Notice period: Not explicitly mentioned in the JD.
Ideal Candidate Profile
- Experienced in regulated medical device software environments and familiar with standards like IEC 62304, ISO 14971, and 21 CFR 820.30.
- Able to independently manage multiple tasks and internal stakeholders, demonstrating accountability and influence without formal authority.
- Comfortable working in remote, virtual, and asynchronous environments with strong communication and collaboration skills.