Job Description
This global, market leading Medical Device Manufacturer have, due to their continued growth and success, a superb opportunity for a Quality System Engineer to join their team based in Slough! This is a permanent position offering flexible working (3 days on site, 2 days from home).
As their new Quality System Engineer, you will be responsible for managing and developing the ISO 13485 QMS, championing Continuous Improvement and Leading the CAPA Process. You will also be responsible for leading and conducting internal audits and supplier quality.
To be successful as the new Quality System Engineer, you will have proven experience in a Quality Systems focused role within the Medical Devices Sector. You will have strong knowledge and experience of leading the CAPA Process, Supplier Quality, Internal Auditing, Risk Management, PMS and Document Control.
Ideal experience required for this role includes;
- Degree educated in Engineering or Scientific Field
- Proven experience in a Quality Systems Focused position with Medical Devices
- ISO 13485 Auditing Qualification
- Proven experience and knowledge of CAPA, Supplier Quality, Auditing, Change Management and Document Control
- Risk Management & Post Market Surveillance experience is highly advantageous
If this feels like the right role for you and you would like to join a company with a defined culture that cares about your development and well-being, please get in touch or apply today!