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Contract

Quality Engineer

Lancashire
money-bag Negotiable
225720773
Posted 2 weeks ago

We are seeking an experienced and motivated Quality Engineer to join a growing medical device business on an initial 6 month contract.

This is an exciting opportunity to play a key role in maintaining and improving quality systems that support the development and manufacture of innovative medical technologies that positively impact patient outcomes worldwide.

Working closely with cross-functional teams including Manufacturing, R&D, Regulatory Affairs, and Supply Chain, you will help ensure products consistently meet regulatory, customer, and business requirements.



Key Responsibilities

  • Support and maintain the Quality Management System (QMS) in compliance with ISO 13485, FDA QSR, and applicable regulations.
  • Lead investigations into non-conformances, deviations, complaints, and CAPAs.
  • Conduct root cause analysis and implement effective corrective and preventive actions.
  • Support internal, supplier, and external audits, including regulatory inspections.
  • Review and approve quality documentation, including procedures, work instructions, and validation reports.
  • Drive continuous improvement initiatives across manufacturing and operational processes.
  • Support risk management activities in line with ISO 14971.
  • Monitor quality metrics and identify opportunities for improvement.
  • Work closely with suppliers to ensure material and component quality standards are maintained.
  • Participate in design transfer, validation, and product lifecycle quality activities.


About You

You will be a proactive quality professional who thrives in a regulated environment and is passionate about delivering high-quality medical devices.

Essential Requirements:

  • Degree in Engineering, Science, Quality, or a related discipline.
  • Experience in a Quality Engineering or Quality Assurance role within the medical device, pharmaceutical, or highly regulated industry.
  • Understanding of ISO 13485 and medical device quality requirements.
  • Experience managing CAPAs, non-conformances, and root cause investigations.
  • Knowledge of risk management and validation activities.
  • Excellent communication and stakeholder management skills.
  • Strong analytical and problem-solving abilities.


Guidant, Carbon60, Lorien & SRG - The Vertage Group Portfolio are acting as an Employment Business in relation to this vacancy.

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