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Supply Chain Supervisor Resume Example

Resume Score: 80%

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SUPPLY CHAIN SUPERVISOR
Professional Summary

Summary: Experienced Professional Individual with 10 years in operations and quality medical device experience. In organizations ranging from start-ups to large corporations. Involved with logistics, operations and strategic planning management for products of high volume disposable devices to development contract manufacturing.

Work History
Supply Chain Supervisor, 09/2015 to CurrentNordson Medical Design & Development - Marlborough, Ma
  • Overseas site manufacturing operations and supply chain planning on commercial and new product development programs.
  • Actively engages in manufacturing to ensure compliance, forecasts and company financial commitments are met.
  • Manages and Monitors a large group of team members, performs performance reviews, motivates and improves team development, function and growth throughout the organization.
  • Coordinates resource personnel to complete workshops, business activities and assignments to SOPs.
  • Manages project audits and project transitions from engineering to clinical manufacturing.
  • Manages Warehouse inventory and material processing flows as well as overseas Shipping and Receiving department.
  • Coordinates logistics and financial department activities to ensure completion of cycle counts, fiscal year counts and material process saving costs.
  • Developed and implemented processes controls of material, logistics and internal work order gathering requests.
  • Developed Value Stream process controls for sustaining production and new product development engineering.
  • Performs site metrics and engages team with KPI's to ensure commitment and performance are met.
  • Improved cost savings for supply chain, logistics and labor.
  • Site SME for ERP Systems Management.
  • Site SME for (IFS) Industrial and Financial Systems integration.
  • Effectively supports R&D Engineering teams to fully meet project demands.
  • Organizes Quarterly Review Boards to drive and improve customer and supplier relations.
  • ISO , BSI , FDA Audit Experience.
  • Site participant leader for company charitable event campaigns.
Operations Manager, 02/2011 to 03/2014Valeritas Inc - Shrewsbury, Ma.
  • (Medical Device, Type 2 Insulin Delivery Device, Managed manufacturing product line to meet daily and monthly goals.
  • Supervised and ensured compliance with protocols and procedures.
  • Functional technical team leader of manufacturing group, consisting of 6 Technicians and 40 Operators.
  • Coordinated and implemented new processes of lab and clean room management.
  • Experienced with R&D engineering support.
  • Communicated with customers, coordinated panel meetings, calls with clients and updated project reports.
  • Reviewed analytical finance reports and executed on improvements to drive cost savings, labor reductions and meet site commitments.
  • Administrated SOPs for GMP medical device productions, protocols.
  • Responsible for documentation of production batch/lot records.
  • Developed and implemented KPI strategic production and quality plans for deviations and change control.
  • 1 Year Technical Validations experience, upon optimal testing of 2nd and 3rd Generation automation machines in overseas development, leading to a diversified exposure in both manual and automated testing of disposable medical devices.
  • Managed a team for annual inventory checks and variances.
  • ISO , BSI , FDA Experience.
  • Internal Audit experience and exposure to regulatory Audits.
Quality Analyst,03/2009 to 02/2011Genzyme Corporation - Framingham, MA
  • Responsible for training and ensure staff compliance with all SOPs.
  • Ensured team was up to date on all safety practices and understood personal safety and that of others.
  • Supported gathering and analyzing of raw materials, drug materials and drug products.
  • Supported PM Scheduling, equipment calibrations and troubleshooting.
  • Executed CAPA investigations and completed within a required time of discovery.
  • Drove KPI metrics to analyze site quality performance.
Quality Supervisor, 04/2008 to 05/2010Advanced Cable Ties / ACT - Gardner, MA
  • Prepared and tested production components to compliance requirements.
  • Excelled in Documented and maintained log books related to inventory, equipment and work flow.
  • Assuring GMP/GDP compliance in lab and shop floor.
  • Solved product related issues and proper coordination with other departments for overall quality and successful production.
  • Created and implemented quality process controls per each product line.
Education
Bachelors, Business Management
Fitchburg State University - Fitchburg, MA
Certification Six Sigma Green Belt - Course: Enrolled
Skills
  • Audit Experience
  • Automation
  • BSI
  • Clients
  • Delivery
  • Documentation
  • Engineering support
  • ERP
  • Finance
  • Financial
  • Functional
  • GMP
  • Internal Audit
  • Inventory
  • ISO
  • Team development
  • Team leader
  • Logistics
  • Materials
  • Meetings
  • Monitors
  • New product development
  • Performance reviews
  • Personnel
  • Processes
  • Protocols
  • Quality
  • Receiving
  • Safety
  • Scheduling
  • Shipping
  • Six Sigma
  • Strategic
  • Supply chain
  • Systems integration
  • Systems Management
  • Troubleshooting
  • Type 2
  • Workshops
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Resumes, and other information uploaded or provided by the user, are considered User Content governed by our Terms & Conditions. As such, it is not owned by us, and it is the user who retains ownership over such content.

Resume Overview

Companies Worked For:

  • Nordson Medical Design & Development
  • Valeritas Inc
  • Genzyme Corporation
  • Advanced Cable Ties / ACT

School Attended

  • Fitchburg State University

Job Titles Held:

  • Supply Chain Supervisor
  • Operations Manager
  • Quality Analyst
  • Quality Supervisor

Degrees

  • Bachelors , Business Management
    Certification Six Sigma Green Belt - Course: Enrolled

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