Regulatory Submissions Associate jobs
Regulatory Affairs Associate Manager
Accountabilities In this role, you lead the regulatory evaluation and approval process for raw materials.. You collaborate with suppliers and internal stakeholders to gather necessary regulatory, technical, and..
Regulatory Associate 80 100 %
Votre nouveau défi Vous travaillez dans une équipe composée de Regulatory Managers et Regulatory Assessors et préparez d'un point de vue administratif les demandes d'autorisation et de..
Junior Associate, Risk & Regulatory Ai Team
Design internal and client facing training programs supporting the upskilling around AI opportunities and technologies of our Risk and Regulatory staff in Engage with clients, leveraging your..
Regulatory Affairs Associate Manager
Position In order to strengthen our Regulatory Affairs team in the Perfumes Department based in Neuchâtel, we are recruiting a talentedRegulatory Affairs Associate ManagerReporting to our..
Regulatory Affairs Manager - (Swiss Submissions, home-based) (m/w/d)
The Manager, Regulatory Affairs International supports ambitious geographical expansion plans.. Indicate sufficient hyperlinking for Swissmedic purposes.Perform Support submissions activities to..
Regulatory Affairs Specialist
This position requires a good foundation in regulatory compliance frameworks within the EU and the.. and 510(k) submissions is advantageous.Additional InformationIntuitive is an Equal Employment..
Regulatory Affairs Associate Manager
Position In order to strengthen our Regulatory Affairs team in the Perfumes Department based in Neuchâtel, we are recruiting a talentedRegulatory Affairs Associate ManagerReporting to our..
Associate Director Regulatory Affairs Biosimilars
Basel.Primary Job Function Prepare, execute, and implement the global regulatory strategy for new.. biotech projects.Be the lead member from global regulatory on behalf of regional and national regulatory..
Clinical Scientist
They are seeking a Clinical Scientist to provide scientific and medical expertise to various products across various stages of clinical development to facilitate regulatory submissions..