in Regulatory Affairs (must have experience with human medicine and biologicals) Experience in product
in Regulatory Affairs (must have experience with human medicine and biologicals) Experience in product
drawings, etc. Coordinate project activities and resources. Participate in commissioning and Factory Acceptance
regulations. - Manage budgets, schedules, and resources effectively to meet project deadlines and budget
Dictaphone and copy-typing of documents Preparing resource and client files Administering and organizing