Description
I am currently shortlisting for a Senior Regulatory Affairs Consultant position with a leading pharmaceutical company based in Scotland (this role is to be based in Scotland with some flexibility for start times on Monday and finish times on Friday). This is a fantastic opportunity to work with one of the worlds leading medical device companies.This role is initially 6 months but is very likely to role on.
Role profile:
This role will support the RA Project Leads for new blood glucose monitoring system development projects.
- Supporting the project RA Lead during characterisation, verification & validation, labelling & claims development.
- Partnering with global regulatory affiliates and providing documentation to support international applications for new products/maintenance of existing product licenses.
Experience:
- An individual with strong regulatory and medical devices experience
If you are interested please call Akeel on ASAP as they are moving quickly, alternatively if you know someone who may be interested feel free to pass on this message. Any successful referral is entitled to £200 vouchers. Looking forward to hearing from you.