A
Executive Manufacturing QMS and compliance Injectable
Amneal Pharmaceuticals, Inc.
Ahmedabad
Full-Time
2-5 Years experience
Description
- 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.
Eligibility Criteria
- Experience: 2+ years
- Seniority: Entry Level
- Education: Bachelor's degree required
- Languages: English
About Amneal Pharmaceuticals, Inc.
Amneal Pharmaceuticals develops, manufactures, and markets generic and specialty medicines worldwide.