2.0 - 6.0 years

0 Lacs

gujarat

On-site

As a Senior Officer Production at Sun Pharmaceutical Industries Ltd., located in API Dahej, your responsibilities will include taking charge from the previous shift by checking Batch Manufacturing Records (BMR) and the status of plant/batches for operation during your shift. It is essential to ensure that all activities are in line with the log report while taking charge from the outgoing officer. Throughout the shift, you must strictly adhere to Good Manufacturing Practices (GMP) norms and promptly report any deviations to your superior. In case of any observed deviations from the process parameters outlined in the BMR, immediate corrective actions should be taken, documented, and reported to the relevant authority. Your role will also involve coordinating with service departments such as Engineering, Quality Control, and Stores to guarantee uninterrupted services. Additionally, you will be responsible for the calibration and verification of weighing balances, as well as overseeing the receipt of raw materials from the store by cross-checking Material Requisition Orders (MRO) and verifying them with all containers of raw materials dispensed for batch numbers. Managing the transfer of solid and process waste to the respective area and maintaining records of such activities will be part of your routine tasks. Furthermore, you will be expected to monitor differential pressure, temperature, humidity, and equipment occupancy records. It is crucial to uphold proper housekeeping standards and ensure that the designated areas are cleaned by the respective personnel. Moreover, you may be assigned other activities as required from time to time, contributing to the efficient and compliant operation of the production facility at Sun Pharmaceutical Industries Ltd.,

Posted 1 month ago

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Microbiology - Jr Executive Promea Therapeutics

1.0 - 5.0 years

0 Lacs

hyderabad, telangana

On-site

You will be responsible for conducting environmental monitoring in the In-Vitro Diagnostics production areas, Large Volume Parenterals production areas, and Microbiology Department. This includes filling out the related documentation for Environmental monitoring. Your role will involve analyzing the sterility test of finished/bulk/raw materials and documenting the results. Additionally, you will be responsible for performing the Bacterial endotoxin test on finished/bulk/raw materials. You will also analyze the Bioburden of bulk/raw materials and maintain detailed records of Temperature monitoring and relative Humidity in the analysis area log book. Water testing is a crucial part of the job which includes testing Raw water, purified water, and water For Injection (MLT and Pathogen testing) and documenting the results. You will also be responsible for conducting Microbial limit tests on raw materials and documenting the findings. Operating the steam sterilizer and vertical autoclave will be part of your duties, including filling out the related documentation for these operations. Another important task will be performing the Bacterial endotoxin test on water for injection. Additionally, you will need to conduct DOP on plates for all sections IVD, LVP, MBD and perform Gram staining tests while maintaining detailed records of these tests.,

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