Jobs 411 bis 420 von 1.167 (dupliziert 1.038)

IT Project Management - 6 months - Germany

Aplitrak
For our international client in Germany we are looking for an IT Project Manager with experience in the Quality and Regulatory domain. Your main task is to drive and manage the implementations and solution design of global
Vor 60+ Tage

RA/QM Spezialist (m/w/d) Medizinproduktehersteller M...

Aplitrak - München
Gehalt: EUR50000 - EUR70000 pro Jahr + verhandlungsfähig Aktuell suche ich für meinen Kunden, ein international agierender Medizinproduktehersteller mit Sitz in München, einen Quality und Regulatory Affairs Manager (m
Vor 60+ Tage - Preview

Clinical Development Expert (MD) - Oncology

Oncology - Sevenig (Our)
basis in Darmstadt. As the Clinical Development Expert, you will be accountable for the review of clinical study data, medical monitoring, and update of regulatory documents. Job Responsibilities: Review of patient level
Vor 60+ Tage

Lead Auditor (439743/004) Germany

Aplitrak - Hamburg
Key responsibilities of the Auditor include: Perform regulatory audits of Clients, as well as evaluations of regulatory submissions which include Technical File Review, according to EU directives. Reviewing corrective
Vor 60+ Tage - Preview

Head of Compliance

Aplitrak - Frankfurt
overseeing the AML/AFC framework. As Head of Compliance You Will: Build and implement Compliance initiatives Have oversight over other European satellite offices Act as main point of contact with regulatory authorities
Vor 60+ Tage

RA Manager (m/w/d) Medizinproduktehersteller Berlin

Aplitrak - Berlin
Gehalt: EUR60000 - EUR85000 pro Jahr + verhandlungsfähig Mein Kunde, ein Medizinproduktehersteller, sucht ab sofort einen Manager (m/w/d) für das Regulatory Affairs, Ihre Aufgabenfelder
Vor 60+ Tage - Preview

Medical Writer (f/m/d) (369821/001) Hamburg, Germany

Aplitrak - Hamburg
freelance basis (f/m/d) Project start: ASAP Project duration: 10 months + Location: Hamburg area Tasks: Facilitate and prepare high quality clinical and regulatory documentation, within established timelines, to
Vor 60+ Tage - Preview

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Vor 60+ Tage

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Vor 60+ Tage