|Publication date:||April 08 2021|
For a global market leader at the forefront of research to deliver innovative health solutions we currently have an exciting opportunity for a Senior Regulatory Affairs & Pharmacovigilance Specialist.
As a Senior Regulatory Affairs (RA) and Pharmacovigilance (PV) Specialist you will be responsible for meeting all RA requirements for obtaining and maintaining local product registration and overseeing activities for the entire product portfolio as applicable. You will collaborate with colleagues to ensure compliance with local laws and regulations which may include but are not limited to: review submission packages, translate and review product information, provide input for local PV and RA agreements, local due diligence activities, participation in audits and inspections and related readiness activities, review of local initiatives for compliance with PV requirements streamline and improve processes, training, communication of safety issues. Besides this, you are responsible for planning of departmental activities and monitoring KPI’s. You will report directly to the PV and RA Country Lead.
Main responsibilities but not limited to;
You will be joining a global dynamic and challenging environment with great opportunities for personal development.
If you are interested in this job, or in similar ones, please feel free to contact me directly.
Principal Consultant | Biotech & Pharma