Executive LIMS

Sun Pharmaceutical Industries

Job Responsibilities:

To have thorough knowledge and understanding of QC workflows (Analysis/ Review/ Approve/ Investigation etc.), Analytical methods (Instrumental/ Pharmacopoeial chapters/ Monographs), QC instrumentation activities (operation, calibration, preventive maintenance etc.) and Analytical method validation/Method transfer activities and other processes of QC.
To have thorough knowledge and understanding of Analysis reporting requirements of all stages of product for eg, but not limited to; Finished product, API, Excipients, Process validation, Hold time, Swab/rinse samples, Stability including result reporting, trending, COA requirements etc.
To support for timely execution and completion of Masterdata activities.
To ensure Masterdata creation and review as per established procedures and ensure updation of masterdata as per the observations, if any.
To list down observations for any discrepancies found during creation/review of masterdata and share to respective team for resolution.
To handover reviewed Masterdata for further process and keep track of closure of observations, if any.
To track Masterdata activity status for creation, review and observation closure etc.
To coordinate masterdata change management to ensure ongoing compliance with business and regulatory requirements.