Sr Off-Qc

2 weeks ago

Sahibzada Ajit Singh Nagar, India SUN PHARMA Full time

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.

  • Sr Off-Qc

    2 weeks ago

    ajit, India SUN PHARMA Full time

    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...

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