Bushan Purushothaman

Senior R & d Engineering Manager, Structural Heart @Medtronic

Santa Rosa, CA, US
MOBILE NUMBERS
+12•••••••87

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WORK HISTORY

Jan 2024 — Present

Senior R & d Engineering Manager, Structural Heart @Medtronic

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Santa Rosa, CA, US

Leading R&D efforts in Structural Heart & Aortic Business for developing new therapies for Mitral and Tricuspid disease states while implementing organizational processes to empower leadership, fostering trust, transparency, and improved team dynamics. Addressed R&D challenges across geographies by streamlining workstreams and enhancing efficiencies, while driving team development initiatives to boost performance and engagement.

EDUCATION

2000 — 2003

Case Western Reserve University

Master's degree, Chemical Engineering

1996 — 2000

Central Electrochemical Reserach Institute

Bachelor of Technology (BTech), Chemical and Electrochemical Engineering

2003 — 2006

Case Western Reserve University

Doctorate, Chemical Engineering

SKILLS

CorrosionMaterials ScienceR&DBiomedical EngineeringMedical DevicesCharacterizationDesign of ExperimentsElectrochemistryFinite Element AnalysisChemistryPolymersBiomaterialsThin FilmsChemical EngineeringResearch and Development (R&D)Scanning Electron MicroscopySpectroscopy

ABOUT BUSHAN PURUSHOTHAMAN

I am an R&D leader with over 25 years of experience, including 17+ years in high-risk implantable medical devices spanning Cardiac Rhythm Management, Heart Failure, and Structural Heart technologies. I currently Lead R&D teams delivering next-generation mitral and tricuspid valve therapies through clinical trials and commercialization within a complex global structural heart portfolio supporting $5B Revenue Franchise. In previous roles, I have led a globally distributed, multi-site engineering and materials organization across the U.S, India, and China supporting a $7.2B annual revenue franchise. My focus is driving predictable execution across complex development programs, regulatory transformation, and enterprise risk mitigation.Throughout my career, I have operated at the intersection of device engineering, materials science, device reliability, and regulatory strategy. I have led cross-functional initiatives involving FDA engagement, EU MDR remediation, and ISO 10993 biocompatibility modernization. Most notably, I directed an enterprise alternate material qualification program for IPG and ICD platforms that mitigated potential $6B annual revenue exposure.In addition to product and regulatory leadership, I am passionate about building high-performing, globally aligned teams. I believe strong organizations are built through clarity of accountability, technical rigor, and developing leaders who can independently drive outcomes.I have been recognized as a Technical Fellow and have represented the medical device industry in AdvaMed and MedTech Europe working groups shaping regulatory standards.I am always interested in connecting with leaders focused on advancing implantable technologies, regulatory strategy, and global R&D execution.

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