*Documentation Management, Review & Approval of the system Standard operating procedure, Equipment Operating procedure, Instrument operating procedure, Area monitoring etc.
cGMP requirements at all stages to meet compliance w.r.t. USFDA, EU, MHRA
Should be wellversed in manufactuirng, experince in oral solids , capsules, injectables is an added advantage.
Experience in cGMP regulatory standards, dealing with agencies internationally.
Possess Very good in communication skills .