Job Description

Primary Function of Position

Responsible for monitoring and control of raw material rejected through a Quality Notification for Non-Conformant Material (Variance Request, VR) generated in the PTC Plants according to the established procedures (DOP’s, SOP’s, WI’s).

Essential Job Duties

• Overall coordination and monitoring tracking/status of all in-house MRB material.
• To contain and segregate non-conforming raw material in the physical quarantine area (MRB) once a Quality Notification (VR) has been created and identifies the material with the attached report and material labels.
• To perform the electronic containment of non-conforming material into quarantined stocking location.
• Interfacing with cross functional teams to provide status of open MRB items and to seek closure on those items.
• Work closely with Planning, Engineering, Inspection, Purchasing, Inventory Control, Finished Goods, Suppliers, Manufacturing and Quality to identify priorities and resolve open issues.
• Ensure that all Quality Notifications are dispositioned in a correct and timely manner.
• Process dispositioned material – Return parts to suppliers, scrap parts, verify tasks completed and approval matrix completion.
• Runs MRB VR dashboard report to determine priorities and assignments for open QN’s Initiates material transfers, reports quality issues, records transactions in SAP as needed to preserve traceability and inventory accuracy.
• Manage and Initiate Purge activities per procedure 859156.
• Maintains the accuracy of identification and count of materials.
• Responsible for maintaining accurate inventory.
• Performs any other projects or duties that may be assigned.

Qualifications

Required Skills and Experience

SAP, Agile, Smartsheet and Dashboards

Preferred Skills and Experience

• Minimum 2-year degree min, prefer BS in Engineering or related field.
• Minimum 2-4 years related experience may substitute for education requirement.
• Requires an understanding of Customer Service, Production, and MRB.
• Previous work experience in Manufacturing, Production Planning or as a Coordinator for a highly complex, low volume OEM manufacturer is desirable.
• Knowledge of GMP and GDP or previous work experience in a medical company are a plus.
• Requires understanding of ERP Information Systems, preferably SAP.
• FDA regulated environment experience preferred.