Notre client, une société de dispositifs médicaux de niche en pleine croissance, recherche un Head of Regulatory Affairs (QP) EU et US pour rejoindre son bureau de Genève. Cette …
Développer et mettre en œuvre une stratégie réglementaire globale alignée sur les objectifs commerciaux de l'entreprise. Surveiller les évolutions réglementaires nationales et in…
Notre client, une société de dispositifs médicaux de niche en pleine croissance, recherche un Head of Regulatory Affairs (QP) EU et US pour rejoindre son bureau de Genève. Cette …
Collaborer à la réalisation du design avec les départements Marketing, Affaires Réglementaires et R&D Etablir les spécifications techniques, les nomenclatures et la codification …
Company Description Sobi offers the opportunity to work at an international pharmaceutical company focused on specialty pharmaceuticals meeting the high medical needs of rare dis…
Provide Regulatory strategies for projects as RA representative in cross-functional teams Responsible for regulatory Assessment on product changes Coordinate the preparation of r…
Output 1: The structure for the guide and the training material are approved by ITC, by May 2024. Output 2: The list of regulations is shared and completed, by May 2024. Output 3: …
The Life Science Career Network CTC are specialised industry experts who can help companies source the best talent and provide reliable HR and consulting services, support varied…
About the Role Do you want to play an active part in managing the relationship with our group-wide supervisor FINMA as well as assessing and mitigating the key regulatory risks a…
BearingPoint is a leading independent management and technology consulting firm in Europe. As part of the strengthening of its activities in Switzerland, BearingPoint is looking fo…
Job Purpose Be a member of product development project-teams from the initiation phase, ensure implementation of quality and Regulatory Affairs requirements for Europe, US & Cana…
Company Description At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, …
Job Purpose Be a member of product development project-teams from the initiation phase, ensure implementation of quality and Regulatory Affairs requirements for Europe, US & Cana…
DESCRIPTION We are open to hire for this role across Munich, Frankfurt,Berlin-Germany; Amsterdam,The Netherlands; Luxembourg ; London, UK; Dublin, Ireland; At Amazon, security …
For our client in Zurich, we are looking for an IT Project Lead (m/f/d) Regulatory Reporting Key Facts Start: 01.05.2024 Dauer: 8 Monate / + Verlängerungsoption Auslastung: 95…
Support team members in creating CE Mark submissions and change notifications to our Notified Body (NB), including responding to regulatory inquiries Aid in the completion and upk…
Support Regulatory Surveillance process with regards to local EU regulation(s); support RA intelligence and regulatory surveillance process Actively engage in process improvement …
Directs the preparation and coordination of comprehensive regulatory submissions for Medical Devices, ensuring compliance with local and international regulations and achieving com…
About the role 26 major approvals, 13 major submissions and 2,000 associates worldwide. That was Regulatory Affairs in 2020. We are a culturally diverse, global team of talented …
Company Description At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, …