Significant experience in quality assurance required, to meet strict regulatory standards for medical devices in the UK and US. A senior position with a high-tech software startup based just outside Cambridge.
You will have:
- A degree in a numerate discipline from a good university
- Significant commercial experience of quality control in a highly regulated environment such as the medical device sector
- The requisite familiarity with ISO 13485 and ISO 27001, in particular, meeting those standards from an engineering perspective
- Excellent people skills
- Experience liaising with governmental and regulatory bodies
You will also need full existing permission to live and work in the UK without time limit, restriction or sponsorship.
Responsibilities include securing clearance and approval in operating jurisdictions, developing and implementing compliance systems across the company, external liaison and follow up, researching new territories’ requirements and keeping abreast of new regulations.
Based just outside Cambridge (west), you will work alongside skilled colleagues in an attractive, modern office environment away from the rush hour traffic. You will also be helping to further a product which can make a real difference in the medical sector. A competitive salary and benefits are on offer.
Interested? Send your CV to ECM Selection; whilst we can only put forward the top few candidates, we do read every CV and try to respond to everyone. Or recommend a friend for £250, details at http://ecmselection.co.uk/tell-a-friend.
Please note: even if you don't have exactly the background indicated, do contact us now if this type of job is of interest - we may well have similar opportunities that you would be suited to. And of course, we always get your permission before submitting your CV to a company.