Deputy Director - Regulatory Affairs and Quality Assurance
Are you looking for a challenging, and worthwhile career opportunity where your contributions will help to accelerate healthcare technology and make a difference in people's lives?
A new opportunity for a Deputy Regulatory Affairs and Quality Assurance Director has become available to join a dynamic, innovative company that operates in the medical device industry.
* Prime responsibility will be to develop the regulatory affairs function to provide expertise.
* You will provide advice on regulatory (and as necessary, quality) requirements to various cross-functional teams in a timely and supportive manner as appropriate.
* Ensure that new products achieve registrations and licences in line with relevant regulatory frameworks to enable and maintain market access. This includes interpretation of requirements; compilation and submission of dossiers and ensuring suitability of product labelling.
* Manage and develop members of the Regulatory Team.
* You will have a degree or equivalent qualification in a science based subject.
* It is essential that you knowledge of regulatory requirements for medical devices including registration, manufacturing and post market controls, in particular ISO 13485 and ISO 14971).
* Effective leadership skills, being able to demonstrate a capacity to develop and grow a team of individuals
* Knowledge of pharmaceutical, biocides and cosmetics regulation would be a distinct advantage.
If you are interested in this position or would like more information then please apply!
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