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Sandoz Private Limited in Telangana seeks a Senior Program Lead– Technology M&A to oversee IT due diligence, Day 1 readiness, TSA execution, and post‑close integration in a pharmaceutical setting.
You will coordinate IT, data, cybersecurity, cloud, and applications with global teams, ensuring alignment with Regulatory and Manufacturing requirements while managing risk and ensuring patient safety.
As a Senior Program Lead– Technology M&A, you will lead the technology workstreams across mergers, acquisitions, divestitures, and integrations within a pharmaceutical environment, from due diligence through execution and post close stabilization. The role is accountable for planning and deliver-ing complex technology outcomes under aggressive timelines, in parallel with commercial, manufacturing, quality, and regulatory deal activities. You will act as the central technology integrator, coordinating IT, digital, data, cybersecurity, infra-structure, and application teams while partnering closely with SSTs (Manufacturing, Quality, Regulatory, R&D, Supply Chain among other business) and external advisors. The role requires a strong understanding of pharma specific technology constraints, including GxP compliance, system validation, data integrity, and regulated manufacturing environments, as well as proven experience working with globally distributed teams.
Lead end to end technology M&A initiatives in a pharmaceutical context, covering IT due diligence, Day 1 readiness, TSA execution, and post merger integration. Own technology integration planning across applications, infrastructure, cloud, data, cybersecurity-ty, and end user services, ensuring alignment with pharma regulatory and quality requirements. Assess and manage GxP relevant systems (e.g., Manufacturing, Quality, Supply Chain, Laboratory, Serialization among others), including validation, data integrity, and compliance implications dur-ing due diligence and integration. Establish and manage integrated technology M&A plans with clear milestones, dependencies, and critical paths, reflecting both deal timelines and regulatory constraints. Lead multiple technology and business workstreams in parallel, including Manufacturing IT, Quality IT, and Corporate IT, ensuring global alignment with deal milestones, contracts as well as global Tech initiatives. Manage tight, deal driven timelines while ensuring operational continuity, regulatory compliance, and patient safety. Identify technology, compliance, and data risks during due diligence and drive mitigation strategies in collaboration with Quality, Regulatory, and Security teams. Prepare concise, executive ready updates for senior leadership and steering committees, translating complex pharma technology risks into business impact. Act as a single point of coordination for internal technology teams and external system integrators, vendors, M&A advisors and M&A Deal Business. Ensure effective handover from deal execution to steady state operations, including validated systems and compliant operating models. Drive clear communication and stakeholder engagement across regions, time zones, and regulated-ed functions.
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Our Purpose here at Sandoz is pioneering access for patients. As the global leader in 'off-patent' high quality medicines, we are able to make medicine more affordable and accessible. Our broad global portfolio comprises of approximately 1,300 quality biosimilar and generic medicines, enabling us to provide more than 900 million patient treatments across 100+ countries per year, and while we are proud of this achievement, we have an ambition to do more! Powered by our talented and ambitious colleagues, who, in return for dedication and skills, experience a flexible, collaborative & inclusive culture where diversity of thought is welcomed and where personal growth is nurtured!