About this role
Key Responsibilities:
- 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.
Other facts
About Amneal
Amneal Pharmaceuticals, Inc. (NASDAQ: AMRX) is guided by a simple belief: essential medicines should be accessible to everyone. What began as a promise to deliver high-quality, affordable medicines has evolved into a diversified portfolio spanning complex generics and injectables, biosimilars, and specialty medicines, including more than 290 products, with scale and capabilities that help reach patients across the healthcare system while combining world-class precision with a deep sense of personal responsibility for every dose we deliver.
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Amneal recommends that you consult with your healthcare provider regarding personal health matters. To report a product complaint or adverse event related to an Amneal product, contact Drug Safety at 877-835-5472, option 3 or [email protected]. If you are currently experiencing a life-threatening event, please immediately contact 911.
What you'll do
- The role involves preparation and review of master documents for sterile manufacturing and managing various compliance-related activities. Additionally, the position requires training staff and ensuring audit compliance on the manufacturing shop floor.
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