1. To plan line wise activity as per production schedule
2. To follow SOPs and minimize the deviations
3.To work with GMP and compliance in manufacturing process.
4.To maintain cleanroom with defined cleaning frequency
5.To report if any abnormality / deviation observed to immediate supervisor.
6.To complete the short term and long-term goals / objective as set by H.O.D.
7.To review document of all operations.
8.To ensure timely execution of batch manufacturing plan.
9.To control the rejection at various stages of manufacturing.
10.To record document of all operations
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.
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