Senior Executive.

1. Analysis of rawmaterial, in-process, finished products stability samples of variousformulation products: oral solids, injectable ophthalmic products.

2. Handling of QCInstruments like HPLC, GC, UV, FTIR, pH Meter, etc.

3. Exposure onsoftware like Empowers, Labware LIMS.

4. Knowledge on theGLP GDP practices.

5. Execution ofvalidation, qualification and calibration activities in QC laboratory.

6. Preparation ofSOP, GTP, STP, specification, protocol, IOCP, record of analysis and analysisreports.

7. Handling, issuanceand maintenance of consumables, glasswares, chemicals, reference standards,working standards and chromatographic columns etc.

8. Preference tocandidates with exposure to regulatory audits like USFDA.

9. To review raw materials, in process, intermediate, finishedproducts, packing material, stability, Hold time samples, qualification,calibration AMT documents.

10. Investigation of OOS test results and laboratory incidences.

11. Ensure the compliance, Safety and 100% Good laboratoryPractice