"• Follow cGMP and GLP practices in Quality Control Lab. • To perform the qualification of working standard. • To Maintain Inventory management for all chemicals, solvents and labo…
"• Receipt of Raw Material for main Pharma stores. • SAP data entries like GRN, Issuance, Transfer posting, reservations, SAP report generation etc. • To check the environmental pa…
Follow cGMP and GLP practices in Quality Control Lab. • To analyze the Sample of raw material on non-chromatographic instrument such as FTIR, UV, Polarimeter, KF, Autotitrator etc.…
Follow cGMP and GLP practices in Microbiology lab- Main pharma QC laboratory. • To analyze the Sample of RM, Validation, FP, in process, Stability for Microbiological analysis by r…
To perform In-process Quality Assurance for the process / products being manufactured and packed in Main Pharma Block (Tablet / Capsule). To ensure Quality and cGMP compliance of t…
Follow cGMP and GLP practices in Quality Control Lab. • To analyze the Sample of In process validation and finish product on non-chromatographic instrument such as FTIR, UV, Dissol…
Ensure the cGMP Compliance and schedule M compliance in production. • Ensure the proper utilization of men and machine of Granulation area. • To ensure the delivery of products as …
"• Follow cGMP and GLP practices in Quality Control Lab. • To analyze the Sample of In process validation and finish product on non-chromatographic instrument such as FTIR, UV, Dis…
"• Ensure the cGMP Compliance and schedule M compliance in production. • Ensure the proper utilization of men and machine of Granulation area. • Ensure the training of production s…
Follow cGMP and GLP practices in Quality Control Lab. •To perform the qualification of working standard. •To Maintain Inventory management for all chemicals, solvents and laborator…
"• Follow cGMP and GMP PRACTICES. • Responsible for charging the stability sample of Finished Product as per SOP. • To follow and maintain stability study schedule. • Pulling out s…
"• Receipt of Raw Material for main Pharma stores. • SAP data entries like GRN, Issuance, Transfer posting, reservations, SAP report generation etc. • To check the environmental pa…
To prepare and review the PQRs. • To compile the quality attributes & In-Process parameter in PQR as per current version of SOP. • To verify & review of Ingredient manufacture name…
"• To prepare and maintain SOP and documents related to Plant preventive maintenance. • To conduct routine breakdown maintenance of Main Pharma Block equipment’s. • To follow and i…
To assure Quality and cGMP compliance of the products being manufactured and Packed for Liquid Manufacturing Block. • To give Area /Equipment clearance i.e. checking and approval o…
"• Follow cGMP and GLP practices in Quality Control Lab. To follow safety procedure in qc department. To analyze the Sample of in process validation and finish product on instrum…
To prepare and maintain SOPs and documents related to plant preventive maintenance. To conduct routine breakdown maintenance of Main Pharma Block equipment. To follow and implement…