ביוטק

CMC RA Manager

74756

תאריך עדכון

16/09/2015

תיאור המשרה

Responsibilities:
Responsible for all CMC RA activities during development of biological product, as well as maintenance of the dossier in approved regions.

Qualifications:
At least 2 years of experience in CMC regulatory.
Experience with biological products.
Experience with FDA.
M.Sc. in a scientific field-a must, M.Sc in biology-an advantage.
High level of English regulatory writing.

המשרה אוישה למשרות נוספות לחץ כאן
המשרה מיועדת לנשים ולגברים כאחד