Walk-In Interview for Officer – QC @ Granules India Limited
Department: Quality Control
Position: Officer
No. of Openings: 20
Experience: 2 – 5 years
Date & Time: 29th August - 31st August, 9 AM onwards
Venue:
Granules India Ltd
Plot no 15A/1,
Phase-III, Jeedimetla,
Hyderabad-500055
Job Description:
- Monitoring of cGLP followed by laboratory personnel during routine operations to ensure adherence to procedure.
- Handling of HPLC , IV.
- Ensuring training of analysts in Laboratory techniques, Quality Control procedures and principles of cGLP / cGMP /General analytical methods instrumentation etc.
- Implementation QMS.
- Qualification of Laboratory Instruments (IQ/OQ/PQ)
- Planning of day to day Laboratory activities
- Maintain Real time documentation and Laboratory safety around the clock
- Review of analytical documents followed as per cGMP and Quality Policies.
- Handling of customer complaints.
- Checking the audit trails and analytical reports.
- Responsible for GLP compliance in the QC Department .
- Preparation and review of Method transfer/Validation protocols
- Review of Instrument Calibration data.
- Handling of Incidents, OOS, Change controls, OOT and all other cGMP record.
- Implementation of CAPAs
- Monitoring implementation of changes as per change control.
- Stability Management
- Preparation and review of specification and test procedures (STPs), General test procedures (GTPs) and cleaning methods.
- Preparation and review of Standard operating procedures (SOPs) and Validation Protocols.
- Review of Analytical Raw data sheets With respect to STPs, GTPs and SOPs.
- Preparation of Certificate of Analysis (COA) for Finished Products, and for Raw materials and intermediates.
- Review of BPCRs
- Preparation and review of Lab Metrics.
- Timely support to the regulatory activities in view of Revision of specifications and Test Methods
- Handling of HPLC , IV.
- Ensuring training of analysts in Laboratory techniques, Quality Control procedures and principles of cGLP / cGMP /General analytical methods instrumentation etc.
- Implementation QMS.
- Qualification of Laboratory Instruments (IQ/OQ/PQ)
- Planning of day to day Laboratory activities
- Maintain Real time documentation and Laboratory safety around the clock
- Review of analytical documents followed as per cGMP and Quality Policies.
- Handling of customer complaints.
- Checking the audit trails and analytical reports.
- Responsible for GLP compliance in the QC Department .
- Preparation and review of Method transfer/Validation protocols
- Review of Instrument Calibration data.
- Handling of Incidents, OOS, Change controls, OOT and all other cGMP record.
- Implementation of CAPAs
- Monitoring implementation of changes as per change control.
- Stability Management
- Preparation and review of specification and test procedures (STPs), General test procedures (GTPs) and cleaning methods.
- Preparation and review of Standard operating procedures (SOPs) and Validation Protocols.
- Review of Analytical Raw data sheets With respect to STPs, GTPs and SOPs.
- Preparation of Certificate of Analysis (COA) for Finished Products, and for Raw materials and intermediates.
- Review of BPCRs
- Preparation and review of Lab Metrics.
- Timely support to the regulatory activities in view of Revision of specifications and Test Methods
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