Austin Vita are currently recruiting a Regulatory Affairs Specialist for a new 6 month contract position supporting a successful Medical Device company. Supporting the client with this key role is a brilliant opportunity to work with an exciting and established business.
As a Regulatory Affairs Specialist you will be supporting the client with the review and generation of technical files as part of the MDD – MDR transition. In addition you will also be responsible for supporting the client with a number of new product registrations.
The core experience the client is looking for centres on the previous Medical Device sector experience and the review and writing of technical files. Experience with Class II devices is essential and any experience with Class III devices would be highly beneficial.
If this position is of interest and you would like to discuss it in more detail, please submit your CV in response. Alternatively, please get in touch on the contact details provided.
Austin Fraser is acting as an Employment Business in relation to this vacancy.
Austin Fraser is committed to being an equal opportunities employer, and encourages applications from candidates regardless of sex, race, disability, age, sexual orientation, gender reassignment, religion or belief, marital status, or pregnancy and maternity status.
Due to the volume of applications received, we are unable to provide individual feedback to unsuccessful applicants.
Salary: £50 – £55/hour
Job Type: Contract
Location: Coventry, West Midlands
To apply for this job please visit www.cv-library.co.uk.