The Regulatory group works with the wider business to translate the constantly evolving requirements of the UK Regulatory environment into the clients policies, procedures, solutions and strategies that ensure compliance and maximize the value for patients.
Do you possess a strong understanding of medical device regulations, coupled with at least 3 years' experience in medical device regulatory affairs and MDR?
We are a global wound care manufacturer, looking to appoint a knowledgeable and experienced Regulatory Affairs Specialist to our growing team.
We are working with a global client whose ethos is plain and simple: we come to work to help be a part of a better future.
If you are looking for a role within a business that inspires self-motivation, commitment and passion then you may just be the perfect missing piece to their team in Welwyn.
Are you looking for a role that makes you feel valued, important and offers you the opportunity to make meaningful and transformative positive impacts on people's lives?
The Regulatory & Quality Director leads a team of technical, regulatory, and quality specialists, to ensure compliance for all regulated activities.
Global Healthcare Company currently seeks a Regulatory & Quality Director to join their team based in Surrey.
This is a broad remit which includes responsibility for government relations, issue management, corporate and social responsibility, strategic communications, and information distribution.