At BioTalent, we are working with a client to fill their newly created QA specialist position. They are a transformative Device company focused on large range of products with a large customer baseThis role will offer youTo work in a fast-paced environment and the ability to take a huge impact.Work closely with their RPA chance to work across a global quality systemExposure to high visibility from the senior leadership team.You will be responsible forSupport both internal and external auditing in a front office facing roleLead QMS updatesSupport documentation updates including risk management and design history filesCoordinate GDP documentationYou will bring the followingHands on Quality experience within a device or IVD products in an ISO13485. Ideal candidates will have experience in pharmaceutical.Worked on internal auditsPrevious track record of updating QMSExperience within GDPExperience within CAPA, Post marketing, NCR, Complaint managementBSc or MSc in a relevant Life Sciences subjectIf you want to be part of an innovative thinking, growing company where you can grow and expand your current knowledge, GET IN TOUCH - Please email me at or on if you think you could be a good match.