Regulatory and Start Up Specialist 1 (Poland)(FSP) page is loaded Regulatory and Start Up Specialist 1 (Poland)(FSP) Apply locations Warsaw, Poland time type Full time posted on Posted 3 Days Ago job requisition id R1419544 ob Overview Perform tasks at a country level associated with Site Activa...
Your tasks will include: compiling and evaluating regulatory files for several countries (EU) tracking and monitoring submissions across all countries translating artworks and monitoring their compliance to all relevant regulations following up on regulatory changes, interpretations, issues respondi...
Your tasks will include: compiling and evaluating regulatory files for several countries (EU) tracking and monitoring submissions across all countries translating artworks and monitoring their compliance to all relevant regulations following up on regulatory changes, interpretations, issues respondi...
As a Regulatory Submission Specialist , you will be responsible for researching medical documents, finding the correct references for pharmaceutical marketing assets, submitting this content into Veeva Vault platform and maintaining internal processes and project management. The role will be perf...
The team is a multi-cultural team based in Frankfurt, Luxembourg, Mumbai and Warsaw, working as one to deliver best in class regulatory reporting to Deutsche Bundesbank & European Central Bank, under a strong and effective control framework. Capital monitoring and regulatory reporting activities ar...
Regulatory Affairs Specialist Warszawa NR REF.: 1183618 Key responsibilities: Preparing registration submissions and post-approval variations for medicinal products Managing CMC (Chemistry, Manufacturing and Control) Variations for Finished Products and Active Pharmaceutical Ingredients Mainta...
As a Regulatory Submission Specialist, you will be responsible for researching medical documents, finding the correct references for pharmaceutical marketing assets, submitting this content into Veeva Vault platform and maintaining internal processes and project management. The role will be perfect
Treść oferty Our Client, an international leader in the healthcare sector, is looking for a (Senior) Regulatory Affairs Specialist to join their ranks. You would join a small global team coordinating and monitoring regulatory submissions across Europe. The team are responsible for personal care...
Regulatory Affairs SpecialistWarszawaNR REF.: 1183618Key responsibilities: Preparing registration submissions and post-approval variations for medicinal products Managing CMC (Chemistry, Manufacturing and Control) Variations for Finished Products and Active Pharmaceutical Ingredients Maintaining Pr...