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Quality System Specialist

Cure Talent Ltd
Posted 11 hours ago, valid for 8 days
Location

London, Greater London W1B 3AG, England

Salary

£45,000 - £55,000 per annum

Contract type

Part Time

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Sonic Summary

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  • Cure Talent is seeking a QMS Specialist for a 6-month fixed-term contract with an innovative MedTech company in Central London, requiring one day a week on-site.
  • The role involves supporting the development and implementation of an ISO 13485 QMS and preparing for external audits.
  • Candidates should have a strong background in Medical Devices and proven experience with ISO 13485, including skills in Document Control, CAPA, and Complaint Management.
  • The position offers a salary of £40,000 to £50,000 per year and requires at least 3 years of relevant experience.
  • This is a great opportunity for a collaborative team player looking to contribute to a rapidly expanding company in health technology innovation.

Location: Central London | Hybrid - once a week on site

Type: 6-Month Fixed Term Contract

Cure Talent is delighted to be working with an innovative MedTech company revolutionising ear and hearing healthcare! With their ongoing growth and exciting projects, we have a fantastic opportunity for a QMS Specialist to join them on a 6-month fixed-term contract.

We are looking for an experienced Quality Professional to support the development and implementation of an efficient and compliant ISO 13485 QMS. You will play a pivotal role in preparation for external audits, assisting various departments, and driving continuous improvement initiatives across the organisation.

The ideal candidate will have a strong, proven background in Medical Devices with experience of implementing or developing an ISO 13485 QMS (eQMS experience is a bonus), SOP writing, Document Control, Change Control, CAPA, Non-Conformance Management & Complaint Management.

Key Responsibilities:

  • Support the QARA Manager in managing and developing the QMS to ensure compliance with ISO 13485, EU MDR, and FDA requirements.
  • Assist departments in identifying, investigating, and resolving non-conformances for software and hardware medical device components.
  • Act as CAPA lead, managing all phases, including root cause analysis, risk evaluation, corrective/preventive actions and closure.
  • Monitor CAPA status to ensure actions are completed in a timely and effective manner.
  • Provide guidance to address audit findings, validate software used in the QMS, and maintain SOPs and quality records.
  • Perform daily QMS management tasks and support warehouse and customer support teams, including occasional travel to Site in Exeter.

The ideal candidate will have the following skills and experience:

  • Proven experience in a Quality role within the Medical Device industry.
  • Strong working knowledge of ISO 13485, EU MDR, and FDA regulations.
  • Experience in Document Control, Change Control, CAPA, NCR, and Complaint Management.
  • Excellent attention to detail with strong communication and organisational skills.
  • A collaborative team player who can work independently when required.

If you're looking for an exciting opportunity to be part of a rapidly expanding company at the forefront of health technology innovation, get in touch today!

Apply now in a few quick clicks

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