Assistant ManagerJobs Opening in Cadila Pharmaceuticals Ltd at Ankleshwar
FEATURED JOBAssistant Manager
Cadila Pharmaceuticals Ltd
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Posted: 09 Jul 26
Job Description
Manage day-to-day operations of the QC laboratory, ensuring adherence to cGMP, GLP, and regulatory requirements.
Review and approve analytical data, laboratory records, specifications, Certificates of Analysis (CoA), and test reports.
Supervise testing of raw materials, packing materials, intermediates, APIs, cleaning validation, water samples, and stability samples.
Ensure timely calibration, qualification, preventive maintenance, and utilization of laboratory instruments.
Oversee analytical method verification, method transfer, validation support, and troubleshooting activities.
Investigate laboratory deviations, Out of Specification (OOS), Out of Trend (OOT), atypical results, and implement effective CAPA.
Ensure compliance with ALCOA+ principles and maintain data integrity in all laboratory activities.
Review analytical documentation for completeness, accuracy, and regulatory compliance.
Coordinate laboratory investigations with QA, Production, Engineering, and R&D departments.
Plan laboratory resources, manpower allocation, and testing priorities to meet production timelines.
Ensure availability of laboratory chemicals, reagents, reference standards, columns, and consumables.
Monitor laboratory KPIs such as sample turnaround time, OOS, OOT, calibration compliance, and instrument utilization.
Job Particulars
Role head quality
Education Any Graduate
Who can apply Freshers
Hiring Process Face to Face Interview
Employment TypeFull Time
Job Id2921234
Job Category Quality Control
Locality Address
State Gujarat
Country India
About Company
Cadila Pharmaceuticals Ltd
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