Regulatory Affairs specialist
My client, a leading regulatory consultancy based in Yorkshire are expanding and looking to recruit a medical devices Regulatory Affairs professional on permanent basis. The role will be based on site.
You will be responsible for
o Responsible for compliance and diligence of product technical product files
o Provide and support advice and technical updates in Medical Device Regulations (MDR) Class 2 & 3.
o Liaise with regulated bodies submissions, queries and clarity.
o Compile and control product technical files for all new MDR product registrations
o Review compliance and update existing product technical files.
o Experience in Post Market Surveillance PMS, collation, review and writing
o Provide input and support to site leadership and business direction
To be considered for a role in Regulatory Affairs, you shoul...