Regulatory affairs director Jobs in Stolberg (Rhld.)
Senior Regulatory Affairs Specialist
MDR (EU) 2017 745) and supporting other departments to comply with these regulatory.. experience as Regulatory Affairs Specialist in the field of medical technology, preferably in an..
Global Regulatory Affairs Team LeaderNonStop Consulting
Global Regulatory Affairs Team Leader Our client, a global leader in agricultural solutions, is seeking.. This pivotal role offers the opportunity to lead a dedicated team of regulatory professionals, shape..
Regulatory Affairs Spezialist (m/w/d)
Ihre Aufgaben Sie sind für die Vorbereitung, Erstellung und Pflege der technischen Dokumentationen für nationale und internationale Produktzulassungen mit Schwerpunkten Europa und ..
Fabrication Director (m/f/d)
About the Job We're looking for an experienced Fabrication Director (m f d) to join one of our portfolio companies and lead its semiconductor foundry. You will work with an experienced fab team..
Technical & Engineering Director
An unserem Standort in Eppelheim suchen wir Dich (m w d) als. TECHNICAL & ENGINEERING DIRECTOR DEINE AUFGABEN Getränkeherstellung,. abfüllung und. verpackung Beaufsichtigung aller Aspekte der..
Head of Product (Regulatory)
Head of Regulatory Affairs & ProjectsLocation. Hybrid. 1 day per week on site in Aachen, Germany.Salary.. Initially taking a hands on approach to writing regulatory documents.Ensure compliance with quality..
Sales Director / Geschäftsführer Frankreich (m/w/d)
Sales Director. Geschäftsführer Frankreich (m w d) Referenz. 1202 SG I.SD Frankreich Für unseren Kunden suchen wir schnellstmöglich einen Sales Director. Geschäftsführer Frankreich (m w d..
Business Consultant - Regulatory, Risk and Compliance (all genders)
StandorteAachen, Augsburg, Berlin, Bonn, Bremen, Dortmund, Dresden, Düsseldorf, Essen, Frankfurt, Hamburg, Hannover, Jena, Karlsruhe, Kiel, Koblenz, Köln, Leipzig, München, Münster..
Assoc. Director Medical / Medical Scientist (m/f/d)
Infectious diseases. Minimum 5 years of pharmaceutical experience internationally in Clinical Development and or Medical Affairs and a thorough understanding of the pharmaceutical industry..