Role: Regulatory Affairs Consultant
Rate: £45-60 per hour
Length: 6 Months
Location: Remote (Site is in South Yorkshire)
Working arrangements: Majority can be done from home, but will need to be on site on for meetings
My client is looking for an experienced Regulatory Affairs consultant to help take a current consumer based product through the new MDR regulations.
The product is a Combination Device, however this role will focus more on the Device rather than the drug.
They ae looking for someone to get them in a comfortable place against the regulation in the next 6 months and provide consultant and advice in regards to testing, specifically lab testing, in line with the Design History Files.
Experience working to MDR
Ability to plan for testing - specifically lab testing - help and advice to meet DHF
Provide a consultative approach
Work on combination devices and drug experience would be a bonus
Flume / Vapour analysis experience
The client is looking for someone to start in October and can be flexible on number of hours/days per week. The work will ramp up the further into the project they get.
The majority of work can be done from home, but travel for meetings o site and potentially other UK sites will be needed.
If interested please submit your CV or call Casey Sedgwick at Real Life Sciences.
To find out more about Real please visit www.realstaffing.com
Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales