. • Removal and destruction of excess packing materials from the line in presence of packing supervisor and QA supervisor...
of area cleaning logs. • To co-ordinate with packing supervisor in relation to the issue related to packing...
of area cleaning logs. • To co-ordinate with packing supervisor in relation to the issue related to packing...
Granulation : • To plan daily Granulation activity per norms of cGMP. • To supervise Cleaning & Granulation activity as per requirement in Cephalosporin block. • To carry out in process checks during Granulation activities. • To arrange bat...
"• 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 implement PPM schedule for effective implementation in shorte...
"• Responsible for small volume parenteral manufacturing activities at Dholka premises. • To check hygienic condition of the workmen before entering to aseptic area, processing area and compounding area and maintain record. • To check and e...
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 parameters like Temperature, RH, pressure difference etc. • Daily...
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 parameters like Temperature, RH, pressure difference etc. • Daily...
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 the products being manufactured and Packed in Main Pharma Blo...
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 parameters like Temperature, RH, pressure difference etc. • Daily...
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 parameters like Temperature, RH, pressure difference etc. • Daily...
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 parameters like Temperature, RH, pressure difference etc. • Daily...
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 parameters like Temperature, RH, pressure difference etc. • Daily...
(1) Received the Finished goods day to day from packaging department. (2) To take GRN entry in SAP after verifies the same with physical stock. (3) Physical dispatches of domestics and export goods as per packing list. (4) Printout the barc...
1. Receive the day to day finished goods from packing department. 2. All transfer ticket entry in SAP. 3. To Export and domestic finished goods physically dispatch. 4. Maintain the Bond Room as per cGmp guideline in routine manner also. 5. ...
Follow cGMP and GLP practices in Microbiology lab-Penicillin QC • To analyze the Sample of RM, Validation, FP, in process, Stability for Microbiological analysis by respective specification and SOP. • To follow safety Procedure in Microbiol...
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. by following test procedure. • To attend the training as pe...
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. by following test procedure. • To attend the training as pe...
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. by following test procedure. • To attend the training as pe...