Head of Pharmacovigilance and Regulatory Rffairs Department/ Responsible for PV / RA

Description of position: Organization of the work of the PV/RA department. Organization of development of documents for the PV/RA department, preparation for passing inspections and audits, implementation of PV/RA system in accordance with the requirements of the GMP EU (GMP MK). Monitoring the work of staff, organization of staff development.

Requirements:

• Higher education in pharmacy – pharmacist (for sure).
• Additional education – specialization in PV (as wish).
• Experience as PV/RA person in pharmaceutical production according GMP.
• Knowledge and experience in the development of PV/RA documentation.
• Analytical skills and attention to detail. Self-motivated with a results-driven approach.