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5.0 - 9.0 years
0 Lacs
hyderabad, telangana
On-site
You will be responsible for routine monitoring of Manufacturing Areas and conducting routine GMP Inspection & review of Quality Records of other departments. Your role will involve monitoring and ensuring that the compliance level of the organization is in line with current GMP requirements. Good Documentation recording and updation will be a crucial part of your responsibilities. Key Responsibilities: - Reviewing URS, DQ, and vendor/suppliers documents related to qualification - Preparing Validation/Qualification protocols and reports - Executing and reviewing qualification/re-qualification and validation activities of Equipment/System/Facility and Plant Utilities - Ensuring adequacy of exe...
Posted 12 hours ago
0.0 years
0 Lacs
hyderabad, telangana, india
On-site
Job Description Responsible for commercial batch release to market Responsible for in process Quality Assurance activities. Responsible for In process Quality Assurance checks during Manufacturing, packing operations. Responsible for line clearance of manufacturing, Packing and dispensing activities Responsible for assurance of cleaning, sterilization and aseptic manipulations of components. Responsible for Sampling of Cleaning Validation & Compilation of the records. Responsible for Sampling & compilation of Process Validation Reports (PVRs) Responsible for sampling and coordination during validation studies (process / cleaning validation). Responsible for routine monitoring of Manufacturin...
Posted 1 day ago
5.0 - 9.0 years
0 Lacs
hyderabad, telangana
On-site
Job Description: You will be responsible for commercial batch release to market and in-process Quality Assurance activities. This includes conducting in-process Quality Assurance checks during Manufacturing, packing operations, and line clearance of manufacturing, packing, and dispensing activities. Additionally, you will assure cleaning, sterilization, and aseptic manipulations of components, as well as sampling of Cleaning Validation & Compilation of the records. You will also be responsible for Sampling & compilation of Process Validation Reports (PVRs) and sampling and coordination during validation studies (process / cleaning validation). Routine monitoring of Manufacturing Areas, good ...
Posted 2 days ago
0.0 years
0 Lacs
hyderabad, telangana, india
On-site
Job Description Responsible for routine monitoring of Manufacturing Areas. Responsible for the routine GMP Inspection & review of Quality Records of other departments. To monitor and ensure compliance level of organization is as per current GMP requirement Good Documentation recording and updation. Responsible for review of URS, DQ and vendor / suppliers documents related to qualification. Responsible for preparation of Validation / Qualification protocol and report. Responsible for execution and review of qualification / Re-Qualification and Validation activity of Equipment / System / Facility and Plant Utilities. Responsible for adequacy of execution of validations being carried out at pre...
Posted 4 days ago
0.0 years
0 Lacs
hyderabad, telangana, india
On-site
Job Description Responsible for routine monitoring of Manufacturing Areas. Responsible for the routine GMP Inspection & review of Quality Records of other departments. To monitor and ensure compliance level of organization is as per current GMP requirement Good Documentation recording and updation. Responsible for review of URS, DQ and vendor / suppliers documents related to qualification. Responsible for preparation of Validation / Qualification protocol and report. Responsible for execution and review of qualification / Re-Qualification and Validation activity of Equipment / System / Facility and Plant Utilities. Responsible for adequacy of execution of validations being carried out at pre...
Posted 4 days ago
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