3 - 4 Years Experience jobs in Belgium (7), Bulgaria (1), Czech Republic (1), Denmark (1), France (2), Germany (7), Hungary (2), Ireland (5), Italy (2), Multiple Countries (4), Netherlands (5), Poland (4), Spain (2), Sweden (1), Switzerland (7) and United Kingdom (11).
A key focus area of the position is the preparation of regulatory CMC documentation for small molecule products during development and commercial stage, in a manner that is scientifically sound, commercially viable and in accordance with current
Own the end-to-end lifecycle of Pharmacovigilance Agreements (PVAs), including development, execution, maintenance, and termination where applicable, along with all associated deliverables. Contribute to strategy setting in collaboration with line
Understand and conduct work consistent with GCP, ICH, 21 CFR Part 11, internal SOPs, and international regulatory requirements; Interact with the project statistician and guide other programmers participating in a project completion
Project management of Cryo-EM projects (Gene-to-Structure) including customer interactions with international Pharma and Biotech companies in the US and EU. Lead the science and manage project teams composed of scientists from Protein Science and