Quality Manager - Medical Devices
£30,000 - £40,000
Great opportunity for a hands-on Quality professional to join one of Cambridgeshire's most innovative medical device manufacturers!
This business have seen rapid growth over the last few years and their unique product is gathering huge amounts of attention across the world. The leadership team is stacked with experience and industry connections, they've recently moved into a brand-new office and are creating brand new roles on a regular basis.
No team management background required here so could be a great chance to achieve your first Quality Manager role,
or equally could be appealing to experienced QM's who would rather spend time focussed on the product.
Due to business growth we are seeking a detail-orientated and methodical-minded individual who has experience of maintaining QMS systems within medical devices. You will be tasked with ensuring all compliance requirements are not only met, but exceeded. This is a key role that supports the global commercialisation of the business and will be paramount in ensuring further business growth.
You'll be reporting into a newly appointed Regulatory Affairs Manager who has got a strong knowledge of the subject matter and will be able to assist you on your journey.
What will you need?
- Confidence with quality assurance processes within a regulated environment
- Background within medical devices or pharmaceuticals
- ISO 13485 experience + ideally 21 CFR 820
If your CV is ready to go please apply now!
For more information please contact The ONE Group's Technical Division on 01733 234000.
This isn't just recruitment, it's recruitment as it should be.