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Tier-1 employer and Hyderabad metro increase competition, but seniority and regulated medical-device focus moderate candidate density.
Regulated medical-device program management requires domain experience, making cross-industry transferability limited.
Explicit 13+ years requirement plus mandatory program leadership and regulated-software experience makes filters stringent.
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Lead medium to high complexity software development programs, managing planning, execution, monitoring, and delivery aligned with business objectives.
Serve as primary coordinator across cross-functional teams and stakeholders, establishing governance and communication processes including status reviews and executive updates.
Analyze program performance data to identify risks, trends, and improvement opportunities while applying Agile, Waterfall, or SDLC methodologies for compliant program execution.
Bachelor's degree in Computer Science, Software Engineering, or Engineering discipline.
13+ years relevant experience including 5+ years leading software development projects or programs.
Experience managing enterprise software, cloud, mobile, or embedded software projects from planning through delivery.
Proficiency with project and program management tools like Microsoft Project, Jira, and Confluence; experience with Agile, Waterfall, or SDLC methodologies.
Experienced in managing complex, regulated software development programs, preferably in medical device or similarly regulated industries.
Strong capability in stakeholder management, risk mitigation, and driving program transparency across global, cross-functional teams.
Comfortable leading programs that require disciplined governance, continuous improvement, and adherence to regulatory standards such as FDA and IEC 62304.