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Quality Engineer

63390
  • £45,000.00 - £55,000.00
  • Yorkshire
  • Permanent

Quality Engineer – Yorkshire, UK – Medical Device – 6-9 Month Contract

 

About the Company:

We are looking for an experienced Quality Engineer from the medical device industry to start at short notice on a 6 – 9 month contract. The role is site based 5 days a week.

Responsibilities:

  • Lead and implement validation programmes, including process, cleaning, sterilisation, and computerised systems validation
  • Develop and review validation protocols and reports, ensuring robust statistical analysis and data integrity
  • Generate and review equipment qualifications and Gauge R&R studies
  • Support site qualification activities aligned to the Master Validation Plan
  • Investigate complex quality and compliance issues, driving root cause analysis and CAPA implementation
  • Lead risk management activities (e.g. FMEA) and integrate risk processes across the product lifecycle
  • Provide quality engineering support to projects, ensuring timely and compliant delivery
  • Drive continuous improvement initiatives to enhance systems, processes, and efficiency
  • Support maintenance, calibration, and equipment compliance systems
  • Participate in internal and supplier audits, ensuring regulatory compliance

Requirements:

  • Significant experience working as a Quality Engineer in the medical device industry.
  • Availability to start with short notice.
  • Ability to work onsite 5 days per week.
  • Eligibility to work in the UK for a full duration of the contract.
  • Excellent communication skills.
  • A good knowledge of ISO 13485.
  • Equipment and process qualification and validation experience.
Claire Collinson Client Director Regulatory, Quality & R&D Recruitment

Apply for this role

  • info@kinetica.co.uk
  • +44 (0)113 261 71 81
  • Kinetica (UK) Ltd, Floor 13, Whitehall Waterfront, 2 Riverside Way, Leeds, LS1 4EH, UK