Regulatory Affairs Consultant Medical Device CDX IVD

Regulatory Affairs Contract job, Combination Products, CDX, IVD, UK and Ire

Your new company
This well-known diagnostics company is looking for an experienced Regulatory Affairs professional to join their established team.
Your new role
The main aspect of this contract job within Regulatory Affairs is to

• Support the team in ensuring that regulatory requirements are met for Clinical Trial Applications that involve Medical Devices of any nature (e.g.: physical devices, digital devices, in-vitro diagnostics, etc)
• Continuously monitor the changes to the UK Regulatory environment and provide an impact assessment on changes to the current framework and/or implementation of new Regulations and be part of Trade Associations (e.g.:ABHI, ABPI, MedTech, etc) working groups and gather regulatory intelligence Keep track of changes and/or implementation of regulations relevant to medical devices, such as (but not limited to) Sustainability/Environment, etc
• Provide support for the implementation/adaptation of the medical device structure across the UK Affiliate

What you'll need to succeed
It is essential that those Regulatory Affairs professionals applying for this role specialise in UK markets and have worked on companion diagnostics and IVDs.
What you'll get in return
Flexible working options are available.

What you need to do now
For more information on this or any other Regulatory Affairs Medical Device contract jobs, please apply to this advert