We're sorry, the job you are looking for at Selvita on EuroPharmaJobs has expired.
Click here to see more jobs at Selvita .
We still have many live jobs. Click below for similar jobs in:
or go to our job search page.
You will lead research programs in collaboration with internal and external partners focused on the development of novel drug candidates for the treatment of chronic liver...
Provide GMP/GDP expertise and supervise the clinical trials supplies within the EU and Switzerland and ensure the correct handling of the IMP (Investigational Medicinal Product)...
You will be responsible for all regulatory activities related to product development and marketing authorizations in the region and is the primary contact point within UCB for any...
In this role, you will be responsible for leading an operational team that provides a range of services related to laboratory analysis within clinical trials for our clients. This...
You will be responsible for leading the Global Quality Management Systems team with responsibility for the Quality Management Systems (QMS). The primary role of this position will...
Lead, manage, and develop multiple laboratory teams, fostering a culture of excellence and continuous improvement. Oversee protein analytical methods, including method development...
Act as a specialist in the area of oncology. Represent Regulatory Affairs internally working on a collaborative basis both within Europe and globally as a member of a...
Provide strategic and technical pharmacovigilance advice to Global Patient Safety (GPS), and other regulatory and medical functions within the Medicines Development Unit; Play an...
Provide DMPK scientific leadership across all stages of the portfolio; Oversee the quality and performance of all DMPK activities including interactions with external CRO’s and...
Manage, prepare, finalise CMC sections of EU IMPD/MAA and rest of world equivalent documents. Oversee teams preparing content, arrange reviews by regulatory, SME peers, senior...
Lead design of preclinical and/or clinical studies needed to support health benefit claims. Author, update and maintain relevant scientific documentation. Work closely with Product...
Responsible for providing strategic regulatory guidance on the global pediatric development in alignment with and within the overall development of a product; Lead multiple...