3 - 8 years
6 - 10 Lacs
Posted:1 week ago|
Platform:
Work from Office
Full Time
Responsible for preparation & review of the master documents of sterile manufacturing for parenteral facility. Responsible for preparation and review of protocols and reports based on the requirements. Responsible for document management and preparation like BMR s, BPR s, master SOP s etc. Responsible for the handling of change control, deviations, CAPA, investigation etc. Responsible to give training to all the subordinates, technicians and operators of the department. Responsible for Audit and compliance on manufacturing shopfloor. Knowledge of kaizen and continuous improvements.
Amneal Pharmaceuticals
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My Connections Amneal Pharmaceuticals
Pharmaceutical Manufacturing
5001-10000 Employees
274 Jobs
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