Posted:3 weeks ago|
Platform:
Work from Office
Full Time
Job Description:
Ensure GMP compliance.
Issue formats & protocols for Process Validation and Hold Time Study.
Prepare protocols and reports for Process Validation & Hold Time Study; compile related data.
Maintain all process validation documents along with batch records.
Perform Process Validation activities on the shop floor.
Maintain qualification records as per requirements.
Execute equipment software and system qualification & re-qualification activities under supervision and coordination with concerned departments.
Prepare QA SOPs.
Ensure discipline within the department.
Handle incidents, deviations, change controls, and CAPA.
Prepare, review, and approve Cleaning Validation Matrix.
Prepare, review, approve Cleaning Validation Protocols and Reports; perform Cleaning Validation activities.
Acme Generics
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