QA Engineer, Medical Device, ISO 13485, 21 Cfr 820

4 weeks ago


Oxford, United Kingdom Corriculo Ltd Full time

**QA Engineer, Medical Device, ISO 13485, 21 CFR 820, COR4929**

**The role**

This is an excellent QA Engineer position, for my client based-in Oxford. The successful QA Engineer will use their knowledge of ISO 13485 and/or 21 CFR820, as well as their experience with Medical devices, to support the development, maintenance and implementationof the businesses eQMS and documentation processes.

**The Company**

The successful QA Engineer will join an Oxford University spin-out within the MedTech sector, who have received strong backing. You will be joining a forward-thinking and supportive environment that encourages inclusion. The current working pattern for theQA Engineer is hybrid based, working in the Oxford office 4 days per week, with 1 day working from home.

**Benefits**
- 25 days holiday + BH
- Flexible working
- Excellent training & progression

**What’s Required?**
- Prior commercial experience within a similar Quality role
- An understanding of ISO 13485 or 21 CFR 820 - knowledge / experience of both would be highly advantageous
- Experience with medical devices, with class ll or class lll medical devices being preferable
- Further knowledge of regulatory requirements for medical devices in the EU is also highly advantageous

**So What's Next?**

**QA Engineer, Medical Device, ISO 13485, 21 CFR 820, COR4929**

Corriculo Ltd acts as an employment agency and an employment business. #INDHIGH



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