Production Support Engineer

Requisition ID
2017-3236
Job Location(s)
Limerick Ireland
Company
Cook Ireland
Position Type
Full Time
Category
Engineering

Overview

The primary purpose of this position is to provide technical support to all manufacturing engineering activities as carried out in Cook Medical. These activities include but are not limited to:

• Equipment transfers from Cook sister companies \ new technology sourcing and introduction.

• Production Support and maintenance activities.

• Lead quality improvement and cost reduction projects.

• Tool design activities.

 

Reporting to: Senior Manufacturing Engineer

 

 

 

 

Find out more about Cook Medical here

Responsibilities

  • Ensure that Production engineering activities are carried out according to company operating procedures, and that a high level of productivity and quality is achieved and maintained.
  • Ensure that all activities carried out are compliant with Cook Medical quality system requirements.
  • Work closely with the Machine Shop to develop jigs, fixtures and tooling to improve production efficiencies.
  • Provide immediate response to Call-out from Production on issues impacting the production of products.
  • Define maintenance and calibration requirements for manufacturing equipment in accordance with Cook Medical’s quality system. Perform maintenance on equipment as required.
  • Prepare, review and approve change requests and other quality system documentation requiring manufacturing engineering sign-off.
  • Plan and execute projects to ensure that project timelines, quality and cost targets are met.
  • Deputise for Senior Manufacturing Engineer.
  • Ensure that Cook’s Code of Conduct is considered in all business matters carried out on Cook’s behalf.
  • Implement Change Requests from Cook donor sites on existing products within manufacturing.
  • Ensure that Cooks Code of Conduct is considered in all business matters carried out on Cook’s behalf.

Qualifications

  • Formal Engineering qualification and/or relevant manufacturing experience (3 + years medical devices preferred).
  • Knowledge of Medical Device Quality Standards ISO13485/FDA, practices and GMP or similar regulated industry standard
  • Good computer skills, knowledge of CAD system an advantage.
  • Willingness and availability to travel on company business.

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