Are you looking for a patient focused, innovation driven company that will inspire you and support your career? We are looking for suitable candidate for our important client, an international medical company offices based in Prague. Join the team as a Regulatory Affairs Specialist for Medical Devices.Key responsibilities:- To assure regulatory support across EEU region- To coordinate cooperation between local regulatory teams and medical device manufacturers in order to assure timely medical device registration- To control management in particular the regulatory impact assessment of Quality Change Requests and their resolution.- To provide documents to local Regulatory teams and to International Support team- To analysist marketing materials from regulatory point of viewWe require:- University Education - Life science, medical science, pharmaceutical, chemistry or biotechnology degree- Basically Regulatory Affair experience is needed- Experiences with regulatory of medical devices are advantage- Excellent English skills (written and spoken), day-to-day communications with the US headquarters- Advanced knowledge of MS Office- Excellent organizational skills and attention to details.ContactJana Krištůfovájana_kristufova@drill.czTel.: +420 735 751 086Zpět na výsledky hledání
