He must know the QC equipment Qualification need
He must know how to review Method transfer documents
He must bed able to evaluate the suitability of method in lab vs Method development
He must know the pharmacopoeal need to comply method related
He must have experience in Pharma sector
He must be able to give training to all concern with respect to GLP/OOS/OOT
He must have good investigation skill and to recommend and upgrade lab for 21 CFR compliance.