Good Afternoon,
My client, a surgical instrument manufacturer based in Maidenhead, require a Regulatory Affairs Specialist to join their exciting, growing business.
This is an immediate vacancy and I am eager to hear from candidates looking for an opportunity to join a fast paced company and forward thinking workforce.
Experience in the following desired;
Medical Device Regulations (MDR)
ISO 13485
MDSAP
CE Marking
FDA
Audits
Class ii Devices
This is an onsite first role – there may be some flexibility for remote work down the line. Please bear this in mind before applying. This is an opportunity to join a Life Science business manufacturing life changing and saving equipment for the global market. Salary dependant on experience up to £65k.
To discuss in detail, please send an up to date CV in response and I will be in contact at the earliest opportunity.