Timothy Davison has joined Qserve as Principal Consultant where he is part of the IVD team. With over 20 years’ experience in the industry, he can perfectly support the IVD team. Timothy has an extensive in IVD and medical device product development, validation and delivery.
“I am passionate about applying my experience in software, AI and IVD product development with a quality mindset to support the introduction of new medical technologies that improve patients’ lives. Having known and worked with Qserve for a number of years I am excited about joining Qserve IVD Team!”
Within the IVD industry Tim has worked on prognostic, predictive, risk stratification, and companion diagnostic assay development and delivery with a focus on complete end-to-end solutions.
There’s a personal profile available on this website where Timothy explains more about his experience and his core competences.
About Qserve Group
Qserve’s mission is to support all medical device and in-vitro diagnostics manufacturers with a practical approach, translating existing regulations to understandable requirements. We serve to guide manufacturers in gaining and maintaining compliance as well as conducting clinical studies as a CRO to ensure safe and quality devices in the most streamlined way possible. Qserve’s global team combines its regulatory and clinical knowledge and experience in the medical device industry, sharing more than 900 years’ worth of combined expertise in the medical field. Having teams in the EU, USA, and China provides a global footprint for global regulatory, clinical, CRO and quality services.
Qserve is constantly looking for consultants at different career levels with experience in regulatory affairs, quality assurance, clinical affairs or auditing in medical devices. Check our current vacancies.