We are very pleased to introduce Jasmin Hunter as a new member of our Qserve global team. Jasmin started May 2018 as a Consultant Clinical & Regulatory Affairs to strengthen the US team.
Jasmin has a broad basis both technically and in the Regulatory and Clinical field. Seven years ago, she moved to the medical device sector, working for a company developing and marketing devices in the respiratory field. This is where she got into the regulatory profession working on risk management, PMS, clinical evaluations. The past few years she was responsible as a product manager for training, technical product support and regulatory compliance toward both FDA and CE certification for Europe.
Given her interest and experience in medical writing, her strength for consulting lies in the first place in clinical evaluation, followed by regulatory work. Jasmin is very enthusiastic to start as a consultant with Qserve, sharing her experience with our customers in projects and expanding her competences working with our global team.
We look very much forward to working with Jasmin on Clinical and Regulatory projects!