Job Description Experience Required: B.Pharm / M. Sc. with 2-4 years of experience in Chemical & Instrumental analysis QC (RM). candidate with exposure of sampling in Isolator shall be preferred. Well versed with CAPA, GMP Documentation, should have exposure to regulatory audits such as MHRA, USFDA etc. Followings will be the responsibilities of the position holder: 1. Sampling of raw material (Exposure to sampling in Isolator) as per defined procedure of Quality Control Lab of Hormone block. 2. To ensure the proper cleaning of sampling booth, sampling utensil and compilation of its records. 3. Analysis of Vendor Approval Samples. 4. Raw material samples sent to outside laboratories with proper documentation and its receiving compliance. 5. Analysis of Raw material, Finished Goods, & stability samples as per defined STP. 6. Preparation of volumetric solution & standardization, preparation of reagent and indicator as and when required. 7. Labeling on approved RM, Rejected RM and related to documentation. 8. Data entry in SAP system. 9. Coordinating and aligning the practices and procedures in line with the COBC requirements
