Supply Chain SME

PB Consulting

Andover, MA

Posted On: Nov 07, 2024

Posted On: Nov 07, 2024

Job Overview

Job Type

Contract - W2, Contract - Independent, Contract - Corp-to-Corp

Experience

8 - 15 Years

Salary

Depends on Experience

Work Arrangement

On-Site

Travel Requirement

0%

Required Skills

  • ERP
  • Supply Chain
  • MES
Job Description
Roles and Responsibilities
  • Provide expert guidance on optimizing end-to-end supply chain processes, including procurement, inventory control, planning, manufacturing, and shipping, leveraging ERP and MES technologies.
  • Oversee and advise on the integration and implementation of Manufacturing Execution Systems (MES) such as Critical Manufacturing, Rockwell, Tulip, and other automation technologies to streamline manufacturing processes and improve production efficiency.
  • Ensure supply chain operations meet all regulatory and compliance requirements specific to the medical device industry, including FDA, ISO, and other relevant standards.
  • Drive continuous improvement initiatives across the supply chain by applying methodologies like Lean, Six Sigma, and Kaizen to enhance processes, reduce costs, and improve quality.
  • Work closely with cross-functional teams including IT, manufacturing, procurement, logistics, and quality assurance to ensure successful project delivery and alignment with business objectives.
  • Provide training and mentorship to internal teams on best practices for supply chain processes, ERP/MES systems, and compliance standards.

 

Required Skills & Experience
  • Strong, in-depth understanding of end-to-end supply chain processes, from planning and procurement to shipping and manufacturing.
  • 8+ years of experience working with ERP systems, specifically in supply chain modules like Planning, Procurement, Inventory Control, Manufacturing, Sales, and Shipping.
  • Proven experience with MES platforms (e.g., Critical Manufacturing, Rockwell, Tulip) and integration of MES into manufacturing operations.
  • Deep understanding of the compliance, regulatory, and quality standards specific to the medical device industry (e.g., FDA, ISO 13485).
  • Knowledge of and experience with continuous improvement methodologies (e.g., Lean, Six Sigma, Kaizen).
  • Strong leadership skills, with the ability to communicate effectively with senior leadership, cross-functional teams, and external partners.

Job ID: PC240447


Posted By

Naincy

IT Recruiter