...Regulatory-, Quality- en Compliance activiteiten. Wat wij bieden: Binnen een professioneel en specialistisch team krijg je de ruimte om deze uitdagende rol als Manager Regulatory Affairs & Quality Ass...
...regulatory affairs and external partners such as legal manufacturers, distribution centers, and the Responsible Person for the medical product segment. You will join a small, dedicated quality team wh...
...regulatory, or procedural aspects of medicinal products. Experience in centralised procedure and liaising with regulatory/public health authorities. Regulatory affairs experience on EU-wide or nationa...
...Regulatory Affairs Specialist who will be responsible for the end-to-end regulatory management of a portfolio of pharmaceutical products, including the preparation, submission, and maintenance of lice...
...regulatory affairs and external partners such as legal manufacturers, distribution centers, and the Responsible Person for the medical product segment. You will join a small, dedicated quality team wh...
...Regulatory Affairs Specialist who will be responsible for the end-to-end regulatory management of a portfolio of pharmaceutical products, including the preparation, submission, and maintenance of lice...
...regulatory affairs and external partners such as legal manufacturers, distribution centers, and the Responsible Person for the medical product segment. You will join a small, dedicated quality team wh...
...regulatory affairs and external partners such as legal manufacturers, distribution centers, and the Responsible Person for the medical product segment. You will join a small, dedicated quality team wh...
...Regulatory Affairs Specialist who will be responsible for the end-to-end regulatory management of a portfolio of pharmaceutical products, including the preparation, submission, and maintenance of lice...
...regulatory affairs and external partners such as legal manufacturers, distribution centers, and the Responsible Person for the medical product segment. You will join a small, dedicated quality team wh...
...Regulatory Affairs Specialist who will be responsible for the end-to-end regulatory management of a portfolio of pharmaceutical products, including the preparation, submission, and maintenance of lice...
...Regulatory Affairs Specialist who will be responsible for the end-to-end regulatory management of a portfolio of pharmaceutical products, including the preparation, submission, and maintenance of lice...
...regulatory affairs and external partners such as legal manufacturers, distribution centers, and the Responsible Person for the medical product segment. You will join a small, dedicated quality team wh...
...Regulatory Affairs within Synres, in co-operation with Coim Regulatory Department. To develop and expand the Synres business and product portfolio, also in close cooperation with businesses within the...
...Manager sits comfortably in the Intellectual Property Team, which is part of the wider Legal, Compliance and Corporate Affairs Team. An incredibly diverse team that helps each other learn, grow and de...