Testing of raw materials, Stability samples, and Finished products.
Recording the analytical data in raw data sheet/protocol.
Ensure standardization of working standards and conduct, preventive maintenance, calibration, and qualification of laboratory instruments as and when required.
Ensure accuracy of document and maintain neat/concise/organized stability record.
Follow the EHS policy, Laboratory procedures and maintain compliance with cGMP requirements.
Initiate the OOS, OOT, and deviation & CAPA in Track-wise software.
Destruction of RM/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 the instrument and standard usage in the respective logbooks/registers.
To perform the analytical method transfer activity.
Preparation of eCOA /SAP COA/ Regulatory COA as per requirement.
Any other Assignment is given by Lab in charge/ Manager Quality Control from time to time.
Work rights
The opportunity is available to applicants in any of the following categories.