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...
. • To ensure implementation of quality policy in compression area. • To ensure the technical training & development of people...
(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...
Ensure the training of production staff and worker. • Ensure the development progress periodically of personals and take necessary corrective action. • To lead the Granulation department with respect to developing the second line. • To ensu...
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...
"• 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...
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 staff and worker. • Ensure the development progress periodically...
To perform the analysis of In-Process, Finish & Stability samples in Penicillin QC lab Dholka. • To ensure current good laboratory compliance and ensuring all SOPs related to Quality Control laboratory are prepared and reviewed/implemented ...
Follow cGMP and GLP practices in Quality Control Lab. • To analyze the Sample of stability on instrument such HPLC, UV, FTIR etc. by following test procedure. • Analysis of Stability Samples as per schedule • To follow safety procedure in Q...
Follow cGMP and GLP practices in Quality Control Lab. • To analyze the Sample of stability on non-chromatographic instrument such as FTIR, UV, Dissolution, DT, Hardness etc by following test procedure. • Analysis of Stability Samples as per...
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 samples from chambers as per the schedule • Maintain all stabili...
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, Dissolution, DT , Hardness etc by following test procedure. • To a...
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...
Validation of computerized system as per regulatory requirement • Data integrity of computerized system • Prepare/Review/Revise SOPs related to computerized system validation. • Prepare/Review/Revise master validation plan for computerized ...
Follow cGMP and GLP practices in Quality Control Lab. • To analyze the Sample of stability on non-chromatographic instrument such as FTIR, UV, Dissolution, DT, Hardness etc by following test procedure. • Analysis of Stability Samples as per...