🏢 Job München Regulatory Affairs - Seite 3

Senior Consultant IT Quality & CSV / Life Sciences (m/w/d) Deutschland Teilzeit Deloitte GmbH … Prozessen z. B. in der Produktion, Qualitätskontrolle oder Regulatory Affairs Reisebereitschaft sowie Deutsch und Englisch sehr gut in Wort und Schrift … Know-how. What impact will you make? Du willst im Bereich Risk Advisory – Regulatory & Compliance innovative Lösungen entwickeln? Unser Team berät unsere … (m/w/d). Standorte: Berlin, Düsseldorf, Frankfurt (Main), Hamburg, Köln, München und Stuttgart. Dein Impact: Als Senior Consultant IT Quality & CSV (m/w/d) …Job MünchenQuality Engineer (m/f/d) München Vollzeit LivaNova … Knowledge is use of statistical application tools e.g., Minitab Regulatory Affairs knowledge is preferable Pragmatic and result-oriented: autonomous, … Quality Engineering pertaining to external suppliers‘ activities Support regulatory audits on site What are we looking for To successfully execute the …Job München Regulatory AffairsJunior Clinical Research Associate München Vollzeit AstraZeneca … and assisting with feasibility activitiesCollaborating with local Medical Affairs and other internal stakeholders, as neededFollowing quality issue … some countries, as required, CRAs are accountable for study startup and regulatory maintenance; tasks may include collection, preparation, review and …Job München

Medical Affairs Advisor Metabolics München Vollzeit AstraZeneca … you will do: The Medical Advisor Metabolics is a member of the Medical Affairs Team and will provide scientific and medical leadership especially for … teams, including support for other functions (e.g. marketing, regulatory affairs, market access, HEOR).The Medical Advisor Metabolics will report …München RegulatoryGlobal Pharmacovigilance Operations Lead (f/m/d) Garching bei München Vollzeit ITM Isotope Technologies Munich SE … (Clinical Operations, Clinical Science, Data Management, Medical Affairs) and external vendors What we offer: A modern workplace and exciting … safety procedures and processes including clinical and post-marketing regulatory reporting requirements Support and/or provide assistance in product filing …Regulatory Affairs