01 Aug
|
Amneal Pharmaceuticals
|
India
01 Aug
Amneal Pharmaceuticals
India
- 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.
Qualification: B.Pharm/M.Pharm candidate with minimum 3-5 years experience in manufacturing QMS/Process review/Compliance.
📌 Executive Manufacturing QMS and compliance Injectable (India)
🏢 Amneal Pharmaceuticals
📍 India