Je bent verantwoordelijk voor de registratie strategie van nieuwe producten. Je volgt actief de relevante (internationale) wet- en regelgeving en normen en ... aangrenzende wetgeving op het gebied van de diensten en producten
Projects simultaneously to very strict timelines report to the Director of CMC Regulatory Affairs Skills Required years regulatory ... affairs experience with understanding of international clinical trials Degree (or equivalent)
Sustainability and quality. Description As Regulatory Affairs Specialist, you are responsible for the timely delivery of regulatory ... applications and the enforcement of regulatory dossiers. You ensure that the product conformity
For the preparation of the documents that feature in the regulatory dossiers/data-packages in order to meet the submission timelines. Ensuring that all ... regulatory aspects on the product safety/Pharmacovigilance and commitments/obligations
RA Director and looking for new challenge? Take look here! Working for Rousselot Darling lngredients means working for an ambitious industry leader in an ... entrepreneurial and no-nonsense industrial environment where
Our committed and engaged employees make that Fujirebio Europe (previously Innogenetics) provides innovative solutions for healthcare all over the world. Our ... products and services allow doctors to make fast and accurate diagnosis
Description) The Regulatory Affairs Registration Manager is responsible for the maintenance of the worldwide vaccine licences. by ensuring ... the planning/dispatch/submission/follow-up/approval of data-packages due to Regulatory Authorities:
Description) The Regulatory Affairs Registration Manager is responsible for the maintenance of the worldwide vaccine licences. by ensuring ... the planning/dispatch/submission/follow-up/approval of data-packages due to Regulatory Authorities:
Description) The Regulatory Affairs Registration Manager is responsible for the maintenance of the worldwide vaccine licences. by ensuring ... the planning/dispatch/submission/follow-up/approval of data-packages due to Regulatory Authorities:
Modis is looking for Regulatory Affairs Manager/CMC writer to work in Wavre. Your daily tasks will be related to the regulatory ... management of products (Vaccines). Your role will be to manage the content of relevant technical/CMC
