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Metro Bangalore and generalist supply chain title increase competition, though medical-device specialization limits applicants.
Medical-device regulatory, ISO/CE/FDA audit experience makes the role less transferable across industries.
Explicit 8+ years, regulatory audits, ERP and team leadership requirements make shortlisting stringent.
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Own end-to-end supply chain operations including procurement, manufacturing, and logistics within a regulated medical device environment.
Lead demand planning, supplier onboarding, manufacturing partners management, 3PL & warehousing, and logistics cost control while ensuring audit-ready processes.
Set up and administer ERP workflows and dashboards; act as supply chain liaison for ISO 13485, CE (MDR), and FDA audits.
8+ years of experience in supply chain or operations across procurement, manufacturing, and logistics.
Proven experience managing teams and budgets/spends.
Strong supplier onboarding, negotiation skills, and hands-on ERP experience for procurement, inventory, and logistics modules.
Work Experience Required: 8+ years in supply chain/operations as specified.
Experienced in regulated medical device or similar compliance-heavy environments to manage audit-ready processes.
Comfortable in a hands-on role combining strategic planning, team leadership, and operational execution across multiple supply chain functions.
Skilled in data-driven decision-making with strong analytical capabilities for dashboard creation and KPI management.