Medical Device Quality Engineer – Validation Lead (Contract)

Kinetica is looking for an experienced Quality Engineer to join their team in York and North Yorkshire for a 6-9 month contract in the medical device industry. The ideal candidate will have extensive knowledge in quality engineering, including validation programmes and compliance with ISO 13485.

This role requires working onsite 5 days a week. You will lead risk management activities, drive continuous improvements, and ensure compliance during audits, all while supporting projects to ensure timely delivery.

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