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Tier-1 brand, metro location, and visible mid-level supply-chain title increase applicant competition.
Requires medical-device regulatory, import, and service-level expertise, limiting cross-industry transferability.
Explicit 7–10 years plus regulated medical-device S&OP and logistics experience raises shortlisting strictness.
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Own end-to-end demand forecasting, supply planning, inventory control, and logistics execution for a portfolio of regulated medical device products.
Drive the S&OP process integrating Commercial, Regulatory, Quality, Manufacturing, Finance and Service to balance service levels, working capital, compliance, and cost-to-serve.
Manage logistics operations including inbound, inter-DC, and outbound shipments with 3PL/4PL partners under ISO 13485 and GDP compliance, tracking key supply chain KPIs.
7–10 years of professional experience in supply chain planning and logistics, ideally in a medical device company.
Bachelor's degree in Engineering, Operations, Supply Chain or related discipline.
Experience with demand planning, supply planning, and logistics in a regulated, multi-channel environment.
Familiarity with CDSCO Medical Devices Rules 2017, Good Distribution Practices (GDP), and ISO 13485 for distribution and storage.
Experienced in executing disciplined S&OP cycles with ability to integrate multiple cross-functional stakeholders in a regulated, import-dependent supply chain.
Analytical and detailed-oriented professional familiar with advanced planning systems (o9, SAP) and capable of building supply chain analytics dashboards.
Strong knowledge of regulatory and quality compliance within medical devices, capable of managing audits and vendor compliance (ISO 13485, GDP).