We are a market leading Medical Device Manufacturer and due to our continued growth, we have an exciting opportunity for a Quality System Engineer to join us.
As our new Quality System Engineer, your key focus will be around the creation, maintenance and ongoing development of the Quality System Procedures, Policies and Documentation.
To be successful in this role, you will have a prior experience of working in a Quality Assurance role within a Medical Device Environment and a strong understanding and knowledge of ISO 13485 and MDD to MDR. Proven experience of working with QMS is a must for this position.
• Prior experience of working in a Quality Systems role in the Medical Device Sector
• Proven experience of creating, maintaining and developing Quality System Policies.
• Strong Knowledge and Understanding of ISO 13485
• Strong Knowledge and Experience of MDD/MDR
• Experience of using an Electronic Document Management System
• Proven experience of conducting internal and supplier audits
• ISO 13485 Internal Auditor (Highly Advantageous)
Permanent, Full Time
- Industry Sector Engineering, Utilities