In Vitro Diagnostic Regulation (IVDR), Quality Consultants has never been more sought after due to the notified bodies constantly making regulatory changes within the space. At Meet, we understand the importance of your role and know the pharmaceutical organisations and medical device companies in need of your credentials. 

Your skillset lends itself to overseeing regulatory management systems and completing the technical documentation of conformity assessments aligned with clinical research. In addition, you look at the quality assurance of various In Vitro Diagnostic medical devices throughout the supply chain. Individuals in this role typically work 6 - 12 month contracts, and each day on the job is different. 

As an IVDR Quality Consultant, you work closely with your employer's Director of Compliance and other executives. Here you will complete gap assessments of IVD medical devices and clinical trials. In addition, you will work with the necessary medical device regulators to implement regulations into the business.

We recognise the value IVDR Quality Consultants bring to the Pharma and Biotech companies spearheading innovation within the space. You have a significant impact on the future of global health within the Life Sciences industry. Across the sector, now more than ever, your services are in demand.