Minimum 1 year Regulatory Affairs experience but significant QA experience in pharma environment Computer Computer literate with prior experience with MS Office, Document Management System and / or Quality Management
years' experience in Regulatory Affairs, preferably in human medicines Demonstrable experience across quality, time and cost standards Competencies: Experience in use of CTD software builder and compilation
Minimum 1 year production experience. Minimum 2 years quality assurance experience (preferably with a multinational) multinational). Experience/exposure to Regulatory Affairs is a recommendation. Experience/exposure to pharmacovigilance
Minimum 1 year production experience. Minimum 2 years quality assurance experience (preferably with a multinational) multinational). Experience/exposure to Regulatory Affairs is a recommendation. Experience/exposure to pharmacovigilance
1-year production experience is advantageous. Minimum of 4-years Quality Assurance experience (preferably with Multinational). Minimum of 2-years' experience in a management role. Experience/exposure to Regulatory Affairs
1-year production experience is advantageous. Minimum of 4-years Quality Assurance experience (preferably with Multinational). Minimum of 2-years' experience in a management role. Experience/exposure to Regulatory Affairs