Quality Assurance & Regulatory Affairs Manager, Medical Devices, Hove, QA & RA Manager
This organisation has been established since for a number if years and is a market leader for manufacturing, developing and supplying Ophthalmic Devices for the sight correction. These devices are supplied to surgeons, opticians and the NHS. Due to rapid expansion they now have an exciting opportunity for a Quality Assurance and Regulatory Affairs Manager to join their team in Hove.
As the Quality Assurance and Regulatory Affairs Manager you will be responsible for the all quality and regulatory issues for products. This will involve ensuring products are to FDA, ISO and GMP standards. You will also look after a team of quality control staff and quality engineers.
The suitable candidate will ideally be educated to a Degree level (or equivalent) within a Scientific Discipline. Previous experience of working to ISO 13485 and FDA standards within the Medical Devices industry is essential for this role. Some Regulatory Affairs experience is also required.
As part of this expanding company you will work in a friendly environment and will receive a competitive salary & benefits package.
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