Senior Executive-Production (Drug Product) Piramal Pharma Ltd

2.0 - 6.0 years

0 Lacs

telangana

On-site

Role Overview: You will be responsible for carrying out filling and packing activities as per BFR, BPR & SOPs. It is essential to follow and maintain current GMP standards in the production area/activities. Your role involves adhering to the day-to-day production schedule to ensure the completion of production activities (filling & packing) as per schedule. You are required to take and follow operating instructions for the shift activities from your superior/Manager. In case of any abnormalities found in the production area/activities, you are authorized to stop the activity immediately and highlight it to the production Manager. It is crucial to maintain manufacturing records online and com...

Posted 4 days ago

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Executive - Production (Drug Product) Piramal Pharma Ltd

3.0 - 7.0 years

0 Lacs

telangana

On-site

Role Overview: You will be responsible for carrying out filling and packing activities in accordance with BFR, BPR, and SOPs. It is essential to maintain current GMP standards in the production area/activities and adhere to the day-to-day production schedule. In case of any abnormalities, you are authorized to stop the activity immediately and inform the Production Manager. Your duties will also include maintaining manufacturing records online, verifying raw materials and packing materials upon receipt, and coordinating with various departments for production-related activities. Additionally, you will be responsible for ensuring cleanliness in the production area, following safety procedures...

Posted 1 month ago

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Executive-Production (Drug Product) Piramal Pharma Ltd

2.0 - 6.0 years

0 Lacs

telangana

On-site

Role Overview: You will be responsible for carrying out filling and packing activities as per BFR, BPR & SOPs, following and maintaining current GMP standards in the production area/activities, and adhering to the day-to-day production schedule. You will need to take and follow operating instructions for the shift activities from your superior/Manager. If any abnormality is found in the production area/activities, you are authorized to stop the activity immediately and highlight it to the Production Manager. It will be your responsibility to maintain manufacturing records online, comply with data integrity practices, and handle tasks such as indenting, issuance, and submission of BFR/BPR. Ad...

Posted 1 month ago

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