Global Supplier Quality & NPI Program Lead

Katalyst CRO

Raynham (MA)

On-site

USD 110,000 - 140,000

Full time

14 days+
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Job summary

Katalyst CRO is seeking an experienced Supply Chain Program Manager / Supplier Quality Engineer to lead global supply chain initiatives for NPI, supplier transfers, and readiness in a regulated manufacturing environment.

The ideal candidate has deep expertise in supplier quality, project leadership, and cross‑functional collaboration across supply chain, operations, manufacturing, engineering and quality, with hands‑on experience in FDA-regulated settings.

Qualifications

  • Bachelor's degree in supply chain, industrial engineering, manufacturing engineering, or related field.
  • 5+ years of experience in Supply Chain Program Management, Supplier Quality Engineering, or regulated supply chain roles.
  • Experience in FDA-regulated or highly regulated manufacturing environments preferred.

Responsibilities

  • Lead and execute global supply chain initiatives including NPI and product launches.
  • Coordinate supplier qualification, onboarding, sourcing, and deployment activities.
  • Drive supplier performance, readiness, and collaboration for launches and transfers.
  • Facilitate cross-functional leadership across Supply Chain, Operations, Manufacturing, Engineering, and Quality.

Skills

Supply Chain Management
Supplier Quality Engineering
New Product Introduction
Supplier Transfers & Deployment Readin
Cross-Functional Project Leadership
Change Management

Education

Bachelor's Degree in a related field

Tools

ERP systems
PLM systems
S&OP/IBP

Job description

Katalyst CRO is seeking an experienced Supply Chain Program Manager / Supplier Quality Engineer to lead global supply chain initiatives for NPI, supplier transfers, and readiness in a regulated manufacturing environment.

The ideal candidate has deep expertise in supplier quality, project leadership, and cross‑functional collaboration across supply chain, operations, manufacturing, engineering and quality, with hands‑on experience in FDA-regulated settings.

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