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Quality Systems Administrator - Medical Devices

WALKER COLE INTERNATIONAL LTD
Posted 6 hours ago, valid for an hour
Location

Cardiff, South Glamorgan CF5 1DR, Wales

Contract type

Full Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

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  • Walker Cole International is seeking a Quality Systems Administrator for a leading global medical device provider.
  • The role involves supporting Quality Management System compliance, training coordination, and document management.
  • Candidates should have relevant industry experience in a similar role within a regulated environment.
  • A strong understanding of ISO 9001, ISO 13485, and FDA regulations is required for this position.
  • The salary for this role is competitive, and candidates should have a minimum of 2 years of experience.

Walker Cole International is supporting a leading global provider of medical devices in their search for a Quality Systems Administrator to join their team. This is an excellent opportunity to be part of an organisation with an international presence and ambitious growth plans.

Key Responsibilities:
  • Support Quality Management System (QMS) compliance, including training coordination and document management.

  • Assist with the implementation and maintenance of Standard Operating Procedures (SOPs) related to record and change control.

  • Support updates to SOPs, work instructions, and policy documents in alignment with ISO 13485, MDSAP, and EU-MDR requirements.

  • Coordinate internal and external audit documentation and general administrative activities.

Candidate Requirements:
  • Understanding of ISO 9001, ISO 13485, FDA, MDD/MDR, and GMP regulations.

  • Relevant industry experience in a similar role within a regulated environment.

  • Proficiency in Microsoft Office and other relevant digital tools.

  • Experience with product documentation and regulatory compliance is desirable.

Apply now in a few quick clicks

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.