Shift Chemist - Pharma Neuland Laboratories Ltd

2.0 - 6.0 years

0 Lacs

hyderabad, telangana

On-site

As a Shift Chemist at the Pharma Manufacturing department, your primary responsibility is to ensure the achievement of the desired production yield of pharmaceutical APIs. This involves ensuring that all production activities in the shift comply with cGMP, cGLP, EHS requirements, and specified operating procedures. Key Responsibilities: - Properly take over shift operations following defined procedures - Follow the Gowning Procedure before entering the pharma area - Indent raw materials from stores and update balance in Material Reconciliation Record - Collect Intermediate material and ensure availability of Utilities before charging the batch - Verify and charge raw material quantities, exe...

Posted 2 weeks ago

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Microbiology - Jr Executive Promea Therapeutics

1.0 - 5.0 years

0 Lacs

hyderabad, telangana

On-site

Role Overview: As an Environmental Monitoring Technician, your main responsibility will be to conduct 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 also 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 analyze the Bioburden of bulk/raw materials and maintain detailed records of Temperature monitoring and relative Humidity in the anal...

Posted 3 months ago

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Officer - Production SUN PHARMA

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 ...

Posted 4 months 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 ...

Posted 4 months ago

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