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Mid-level generalist DevOps/software role in Bangalore at a well-known employer with broad requirements, highly competitive.
Medical-device regulatory and IEC/FDA expectations increase domain bias despite transferable SDLC/DevOps skills.
Explicit years, SDLC/regulatory expectations and DevOps tool requirements create moderate shortlisting filters.
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Lead software lifecycle projects of minor scope, ensuring adherence to timelines, deliverables, and compliance with procedures and industry standards.
Responsible for software deliverables, release scheduling, and authoring project documentation; support larger software projects under senior leaders.
Collaborate cross-functionally and with vendors to facilitate software updates, manage post-market changes, and ensure regulatory and cybersecurity compliance.
Bachelor's degree in Computer Science or related field with 3 years experience, or 5 years relevant experience.
Knowledge of FDA/ISO regulations for software development; preferably IEC 62304 compliance understanding.
Experience with SDLC and DevOps tools like Confluence, Jenkins, AWS, Azure DevOps, Jira, Git, GitHub, TFS, and Microsoft Visual Studio.
Work Hours: 1 PM to 10 PM IST; medical device domain experience preferred; notice period: Not explicitly mentioned in the JD.
Experienced in managing software development lifecycle in regulated medical device environments with knowledge of relevant standards and regulations (21 CFR 820.30, ISO 13485, IEC 62304).
Comfortable operating in cross-functional, virtual, and remote teams, coordinating across multiple stakeholders including external vendors.
Skilled in project management and software release coordination within complex, compliance-driven settings involving cybersecurity and regulatory updates.