When you ask for someone with ISO 13485 knowledge and CAPA experience, we will send you people that match your brief not someone from another sector.  If you ask for a Regulatory Affairs Manager with FDA 510k knowledge, we will make sure this is what we supply.

The Quality Assurance & Regulatory Affairs role we recruit for include standards in the UK, Europe, USA and worldwide regions.

So, if you are looking for a new Quality Engineer, Design Assurance Specialist, Product Manager, Regulatory Affairs Manager, Validation Engineer, QARA Directors or other roles that need specific Medical Devices Quality Assurance or Regulatory Affairs knowledge please get in contact by clicking here or calling on 0121 268 2240.