Nine Twenty's client is a manufacturer of medical devices from raw material manufacture to sales of finished devices. As part of a ongoing drive to strengthen the QA group, they have a requirement for an experienced Quality Manager to join them at their Livingston site.
The purpose of the role will be to drive process improvements and quality projects, including the implementation of an electronic QMS and FDA readiness. You will be responsible for ensuring that the site is compliant, and benefits from ISO 13485/ ISO 9001. As well as managing projects you will work with staff throughout the site to investigate root causes and aid improvements to products and processes. You will guide the culture of improving processes and ensuring accountability.
Who we are looking for:
- Degree qualified (or equivalent) in relevant scientific/quality assurance/technical field
- Work experience from pharmaceutical or medical device industry, specifically in a Quality role
- Good understanding of either ISO9001 and/or ISO13485
- Focussed on the principles of the ISO standards and not merely compliance to them
- Excellent communication skills
A fantastic package is on offer, as well as the opportunity to influence and shape the future of this organisation.