Overview:
Cambridge Heartwear Ltd, is looking for a Regulatory Affairs Manager who has experience in working with Class 2a devices within a medical environment.
The Regulatory Affairs Manager will act as the critical liaison between our company, the product we sell and the regulatory authorities. As well as be expected to have knowledge and experience with pre- and post-market medical device regulations.
The Regulatory Affairs Manager will have ECG device experience and FDA lead experience, regulatory and quality management experience within a medical device environment.
The Regulatory Affairs Manager will have a FDA 510K experience; experience with working with medical devices and also regulatory experience of 60601-1.
Job description
Core job responsibilities
Provide regulatory expertise to scientists and senior management and assist with the preparation and submission of regulatory documentation.
Support the maintenance of regulatory files and tracking databases to ensure prompt and accurate access to company regulatory information (concerning current, pending and future approvals and renewals)
Ensure that our heartsense device comply with the regulations of the regions where they want to distribute them.
Keep up to date with national and international legislation, guidelines and customer practices.
Collect, collate and evaluate scientific data from a range of sources.
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