Quality Control Officer

Posted 11 May by REED Procurement & Supply Chain
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Have you worked in Quality Control? Do you have a background in Life Sciences or Medical Devices? Are you a passionate and committed individual?

REED are delighted to be assisting our well-valued life sciences client based in Newcastle on the appointment of a Quality Control Officer based in Newcastle.

This is a full-time and permanent role working 09:00-17:30 although due to the current climate with Covid, there will need to be flexibility in these hours initially. The role is offering £20,000 - 25,000 DOE.

Job Role;

  • Responsible for helping to maintain and improve the Quality Management System by employing excellent attention to detail and managing time efficiently
  • Check incoming material documentation/certification
  • Physically inspect incoming materials
  • Support the Engineering and Assay teams in testing of incoming materials and assisting with non-routine analyses.
  • Perform investigations where required
  • Perform finished product testing according to test methods and product specifications 
  • Help to develop, validate and the perform finished product test methods to facilitate QC testing of instruments and consumables
  • Liaise with the Purchasing and Sales teams to ensure all materials released in time for use
  • Help to generate and maintain incoming material specifications
  • Work with the Operations team to suitably oversee controlled temperature shipments of samples and products
  • Input into supplier complaints where required
  • Ensure all documentation for incoming materials is completed promptly and made available by PDF for batch review
  • Assist with management of outsourcing raw material identity testing
  • Raise QMS documentation for Deviations, Change Control, Supplier Complaint where relevant for incoming material QC
  • Assist with management of laboratory supplies
  • Effectively interact with Technical, Development, Manufacturing, Operations, Sales and Marketing and Planning team

Person Specification;

  • Minimum of 2 years' experience working within a Quality Management System
  • Experience of working with ISO 13485 would be desirable
  • Good attention to detail
  • Proficient in Microsoft software packages
  • Proven experience in a controlled environment of document checking and review

Reference: 40332796

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