eutical production experience or exposure to supplement regulatory knowledge.
data, however additional sources may be used to supplement the investigation. The fellow will research state-of-the-art
data, however additional sources may be used to supplement the investigation. The fellow will research state-of-the-art
eutical production experience or exposure to supplement regulatory knowledge.
Key
eutical production experience or exposure to supplement regulatory knowledge.
Key
eutical production experience or exposure to supplement regulatory knowledge.
Key
calibration of instruments is maintained.
to a QA Manager Liaise with Client's safety representatives on a regular basis, on behalf of the Company Company Schedule and attend site safety representatives, committee and toolbox meetings Schedule and conduct
GMP in-house training. Act as an authorized representative for medical devices. B. Pharm degree with at
relationship building skills High capacity to represent the brand High degree of client engagement Ability