At a Glance
- Tasks: Lead quality engineering activities and ensure compliance with industry standards.
- Company: Innovative medical devices company based in Didcot.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on continuous improvement and innovation.
- Why this job: Make a difference in healthcare by ensuring the quality of life-saving devices.
- Qualifications: Experience in quality engineering and knowledge of ISO 13485 and 21 CFR Part 820.
The predicted salary is between 40000 - 50000 Β£ per year.
Didcot-based medical devices company seeks a Quality Engineer to own core Quality Engineering activities, including CAPA, non-conformities, complaints, change control and audits, ensuring ISO 13485 and 21 CFR Part 820 compliance.
You will contribute to e QMS rollout, supplier quality management and manufacturing quality improvements while collaborating with Engineering and Development teams.
Familiarity with MDR/UKCA is advantageous.
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Quality Engineer - Medical Devices, CAPA & Compliance Lead employer: Energy Jobline CVL
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