Class III Medical Devices. As the Regulatory Affairs Manager, you will be responsible for designing and executing regulatory strategies to bring the company's devices to market. You will play a key role in leading submissions

Regulatory Affairs (w/m/d) mit folgenden Aufgabenschwerpunkten • Die Betreuung des Themas Biologische Sicherheit nach ISO 10993, die Erstellung von Berichten für Intern, Kunden und Behörden sowie die Prüfung und Bewertung

Regulatory Affairs (w/m/d) mit folgenden Aufgabenschwerpunkten • Die Betreuung des Themas Biologische Sicherheit nach ISO 10993, die Erstellung von Berichten für Intern, Kunden und Behörden sowie die Prüfung und Bewertung

Overview: We are seeking a Director of Regulatory Affairs to play a pivotal role in shaping and executing regulatory strategies for specific projects within our organization. This role involves collaborating closely with

) • A Study of Regulatory Affairs in medical devices, Optics, Engineering, International Business Administration, Quality Management or similar • Preferable, internships or working student jobs • An independent

regulatory database. Our team provides product-specific data globally. • As substance coordinator, you are responsible for dedicated substances as main contact for questions related to Chemical Regulations within and outside BASF

promotional activities across international markets, ensuring alignment with business objectives and regulatory requirements. Collaborate closely with cross-functional teams, including product development, sales, regulatory affairs

institutions. • Manage the end-to-end process of organizing events, panels, and conferences, including conceptualization, planning, execution, and post-event analysis. • Planning and monitoring PR activities to enhance

von der Produktdefinition bis zum Market Launch • Unterstützung von Clinical/Regulatory Affairs Teams weltweit bei der Produktregistrierung • Verantwortung für die Anpassung und Verbesserung von Clinical Affairs Prozessen • regelmäßige

von der Produktdefinition bis zum Market Launch • Unterstützung von Clinical/Regulatory Affairs Teams weltweit bei der Produktregistrierung • Verantwortung für die Anpassung und Verbesserung von Clinical Affairs Prozessen • regelmäßige

von der Produktdefinition bis zum Market Launch • Unterstützung von Clinical/Regulatory Affairs Teams weltweit bei der Produktregistrierung • Verantwortung für die Anpassung und Verbesserung von Clinical Affairs Prozessen • regelmäßige

for existing and new products in cooperation with the marketing, medical and regulatory affairs teams • Generation of global value dossiers and value communication tools for existing and new products • Support and

for existing and new products in cooperation with the marketing, medical and regulatory affairs teams • Generation of global value dossiers and value communication tools for existing and new products • Support and

for existing and new products in cooperation with the marketing, medical and regulatory affairs teams • Generation of global value dossiers and value communication tools for existing and new products • Support and

), and other functions such as Operations, Regulatory Affairs, and Quality Management • Monitor monthly sales results and constantly evaluate market effectiveness of workflow solutions and associated business models

), and other functions such as Operations, Regulatory Affairs, and Quality Management • Monitor monthly sales results and constantly evaluate market effectiveness of workflow solutions and associated business models

), and other functions such as Operations, Regulatory Affairs, and Quality Management • Monitor monthly sales results and constantly evaluate market effectiveness of workflow solutions and associated business models

), and other functions such as Operations, Regulatory Affairs, and Quality Management • Monitor monthly sales results and constantly evaluate market effectiveness of workflow solutions and associated business models

), and other functions such as Operations, Regulatory Affairs, and Quality Management • Monitor monthly sales results and constantly evaluate market effectiveness of workflow solutions and associated business models

prüfen Sie die fehlerfreie und konsistente Umsetzung • sich darüber hinaus u.a. mit den Abteilungen Entwicklung, Technologie, Auftragsabwicklung und Regulatory Affairs zur Stammdatenausprägung abstimmen, auch über Standort