Job highlights
. To ensure and control Valuable laboratory practicesin QC laboratory . .

Responsible to analysis of in process, FinishedProduct, Stability, raw material, Packing material and water samples. Responsible to prepare and review of Stabilityprotocol analytical method validation protocol/Analytical methodverification/cleaning validation and their report.

Responsible to review of finished Product, inprocess, Stability, raw material and water. Volumetric Solution Log bookentries

Responsible to analysis and review of standardsqualification for working standard impurities.

Responsible to perform and review of allinstruments calibration and PM activity.

Responsible to conducting training program to QCpersonnel.

Responsible to maintenance of Controlsamples/Stability chamber with samples.





Responsible to preparation review of Specification ,Standard testing procedure(STP),ARDS and of Standard Operating Procedures (SOP s) for Packing material, Raw material, IN-processand Finished products.

Responsible for preparation and review of LogBooks / Sheets.

Responsible to prepare and review ofinstrument/miscellaneous Qualification (IQ, OQ, PQ) protocols andreports.

Responsible to review of in process, FinishedProduct, Stability, raw material, Packing material and water samples.

Responsible to initiate the change control,deviation, . Incident.

To ensure and control Valuable laboratory practicesin QC laboratory

Responsible for any other job responsibilitiesas and when assigned by Senior or HOD from time to time.

📌 Executive Bengaluru (India)
🏢 Ray Life Sciences
📍 India