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Quality Engineer

In Oklahoma / United States

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Quality Engineer   

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JOB TITLE:
Quality Engineer
JOB TYPE:

JOB SKILLS:
JOB LOCATION:
Oklahoma City Oklahoma / United States

JOB DESCRIPTION :

Responsibilities:

  • Responsible for maintaining the quality management system procedures for the Leamington Spa facility. Administer Leamington Spa supplier management system.
  • Responsible for the management and maintenance of the Supplier management system
  • Responsible for the management and maintenance of the document management system in relation to supplier management
  • Lead in the creation and running of the internal supplier management system and Supplier audit program
  • Perform supplier audits
  • Responsible for the management of supplier quality agreements.
  • Responsible for the management of the CAPA system in in relation to Suppliers
  • Preparation of Quality performance reports
  • Domestic 20%; International - Rarely

Required:

  • 4-7 years' experience in Medical Devices, regulatory affairs/compliance. ISO13485
  • Communication, assimilation of data, working relationships across divisions. ISO9001, ISO13485 lead auditor

Position Details

Apr 17, 2021
S16174661736453774
Oklahoma / United States
Oklahoma City
A job sourcing event
In Dallas Fort Worth
Aug 19, 2017 9am-6pm
All job seekers welcome!

Quality Engineer    Apply

Click on the below icons to share this job to Linkedin, Twitter!

Responsibilities:

  • Responsible for maintaining the quality management system procedures for the Leamington Spa facility. Administer Leamington Spa supplier management system.
  • Responsible for the management and maintenance of the Supplier management system
  • Responsible for the management and maintenance of the document management system in relation to supplier management
  • Lead in the creation and running of the internal supplier management system and Supplier audit program
  • Perform supplier audits
  • Responsible for the management of supplier quality agreements.
  • Responsible for the management of the CAPA system in in relation to Suppliers
  • Preparation of Quality performance reports
  • Domestic 20%; International - Rarely

Required:

  • 4-7 years' experience in Medical Devices, regulatory affairs/compliance. ISO13485
  • Communication, assimilation of data, working relationships across divisions. ISO9001, ISO13485 lead auditor