Title: Senior Officer-QC
Date:
Nov 18, 2024
Location:
Mohali - Quality Control
Company:
Sun Pharmaceutical Industries Ltd
RESPONSIBILITY:
- Analyze Finished Product/Stability/Validation/In-process/Swab Samples as per approved specification and standard test procedures.
- Recording the analytical data in raw data sheet/protocol.
- Ensure standardization of working standards and conduct, preventive maintenance, calibration, qualification of laboratory instruments as and when required.
- Ensure accuracy of document and maintain neat/concise/organized stability record.
- Follow the EHS policy, Laboratory procedure and maintain the compliance to cGMP requirements.
- Initiate the OOS, OOT and deviation & CAPA in Trackwise software.
- Destruction of Finished Product/Stability/Validation/In-process/Swab samples after completion of analysis and review of the data.
- Ensure integrity, accuracy and adequacy of the analysis performed.
- Recording of instrument and standard usage in the respective log books/registers.
- To perform the analytical method transfer activity.
- Preparation of eCOA /SAP COA/ Regulatory COA as per requirement.
- Any other Assignment given by Lab in charge/ Manager Quality Control from time to time.