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2.0 - 6.0 years
0 Lacs
ahmedabad, gujarat
On-site
As a responsible team member in the pharmaceutical manufacturing process, your role involves the following key responsibilities: - Conduct line clearance activities before starting various operations such as dispensing, manufacturing, filling, inspection, sealing, labeling, and packing. - Perform process validation, cleaning validation/verification, hold time study, media fill, and routine batch sampling according to protocol/SOP. - Review executed Batch Manufacturing Records (BMRs) and Batch Packaging Records (BPRs). - Perform in-process tests at different stages as per batch documents/SOP. - Review environmental monitoring and water trends. - Review different types of calibration certifica...
Posted 1 month ago
3.0 - 7.0 years
0 Lacs
bhubaneswar
On-site
You will be responsible for managing the overall process of functional and visual inspection of vehicles before dispatch. This includes ensuring stringent checks and inspections are conducted, which also includes thorough cleaning and washing of the vehicles. Your duties will involve inspecting all completed work, ensuring proper documentation of all work, and reporting any deviations to the Manager. Additionally, you will be required to test-drive the vehicles to ensure they are operating as designed. As part of your role, you will need to perform in-process testing and inspection to ensure that parts and assemblies meet production specifications and standards. You will also be responsible ...
Posted 2 months ago
2.0 - 6.0 years
0 Lacs
ahmedabad, gujarat
On-site
You will be responsible for conducting line clearance activities before starting various operations such as dispensing, manufacturing, filling, inspection, sealing, labeling, and packing. Additionally, you will perform environment monitoring activities and ensure compliance with cGMP at the shop floor. Your role will involve process validation, cleaning validation/verification, hold time study, media fill, routine batch sampling, and in-process testing at different stages according to batch documents and SOPs. You will review executed BMRs, BPRs, environment monitoring data, water trends, printouts (CIP, SIP, autoclave, filter integrity), and different types of planner and calibration certif...
Posted 2 months ago
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