Cadila Pharmaceuticals

• 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 (Vendor Name) &

• 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 Tempe

. Responsible for operating vial/bottle and ampoule washing, filling and capping machine and PFS filling Machine at Dholka premises. • Should have knowledge of Operating and maintenance of vial/bottle

•To review Registration and Re-Registration Dossiers before submission in all Aus / NZ countries. •To maintain Country-wise registered products status for all AUS/ NZ countries. •To co-ordinate wit

Responsibility  Lab demonstration & scale up of new DMF and NDMF molecules, Process Optimization before Scale-up activities, Execution of Kilo Lab batches & technology transfer activity. Princ

• Ensure receipt and on-line documentation of the materials received as per SOP. • Ensure all the operating systems are maintained as per the SOP. • To receive the materials as per the amended appro

• 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 instrument such HPLC, GC

• To review Daily Packing plan for the assigned Packing line activities. • To ensure that arrangement of dispensed batches for the day in advance. • To ensure that Daily/Weekly/Monthly packing sche

• 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 laboratory required i

Production : • To check the labels of raw material, packing materials and solvents before usage. • To maintain storage conditions of raw material/intermediates in plant. • To maintain process condi