Technical Programme Manager - Planning

Our client is an AI-driven healthcare technology company transforming cardiovascular care through innovative AI solutions.We are looking for an experienced Technical Program Manager to lead complex cross-functional programs supporting the development of AI-powered healthcare products in a highly regulated environment.Lead end-to-end delivery of multiple technical programs from planning through successful execution.- Drive cross-functional collaboration across Engineering, Product, Clinical, Data Science, Regulatory, Quality, and Business teams.- Develop and manage project plans, timelines, milestones, risks, dependencies, and deliverables.- Ensure project documentation complies with regulatory and quality standards, including Good Documentation Practices (GDP).- Track program progress using Agile methodologies and project management tools such as JIRA and Confluence.- Identify risks, resolve escalations, and proactively drive issue resolution.- Mentor project teams and foster a collaborative, high-performance culture.Required Skills :- 5+ years of experience in the IT industry with at least 2 years in Technical Program or Project Management.- Proven experience managing multiple cross-functional technical programs simultaneously.- Strong stakeholder management and client-facing communication skills.- Experience working in Agile environments using JIRA and Confluence.- Good understanding of software development lifecycle (SDLC), product architecture, and technical delivery.- Strong planning, problem-solving, risk management, and leadership capabilities.Mandatory Experience (Any of these) :- Healthcare Technology (HealthTech)- Medical Devices- Life Sciences- Clinical Software / Digital Health- Regulated Product Development Environment- Candidates without exposure to regulated healthcare or medical device programs are unlikely to be a fit.Preferred Qualifications :- Experience managing AI, Machine Learning, Data Engineering, or Analytics programs.- Knowledge of Good Documentation Practices (GDP), medical device quality processes, and external audits.- Exposure to Design History Files (DHF), FDA-regulated products, or Software as a Medical Device (SaMD).- PMP certification or familiarity with PMBOK methodologies.- Technical exposure to Python/R or NoSQL technologies is an added advantage.Education :- Bachelor's degree in Computer Science, Engineering, Information Technology, or a related discipline.- A Master's degree is a plus. (