Assistant Manager
• Review of analytical data of scale up and validation batches, commercial batches of finished products and also of raw materials, packing material, in process, intermediate, hold time study, stabili
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• Review of analytical data of scale up and validation batches, commercial batches of finished products and also of raw materials, packing material, in process, intermediate, hold time study, stabili
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
"• Responsible rDNA manufacturing and parenteral mfg activities at Dholka premises. • To do aseptic area entry exit procedure properly with proper gowning. • To check and ensure that differential pr
"• Cleaning and operation of Coding and data matrix Coding Machine. • Cleaning and operation of Coding Machine. • Clearance of coding area and machine. • Preventive maintenance of coding machine.
• 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) &
Role Objective: - 1.Operating machines and ensuring the cGMP compliance in primary packing almac machine area area Key Responsibilities: •To check and ensure proper operation of the machine in his res
• 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 , Har
"• To ensure achievement of planned productivity with quality compliance in respective shift. • Work allocation & proper utilization of men & machine. • Co-ordination with Tablet Mfg./Secondary pack
Production : • To take instruction from plant-in-charge for batch charging / monitoring • To report any deviation / discrepancy in plant / process to plant in charge • To ensure completion of batch
"• Ensure all the operating systems are maintained as per the SOP. • Check the environmental condition of dispensing area, RLAF diff. pressure and record the same. • Calibration of all weighing bala
"• 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 labor
Experience 12+ years in Software Quality Assurance, with significant experience in API testing and test automation. Job Overview We are looking for an experienced QA Manager to lead quality engin
Experience 5–10 years of experience in API manufacturing, preferably in a regulated pharmaceutical manufacturing environment. Job Overview Responsible for managing day-to-day production activitie
1. Planning and execution of Validation, Qualification, Re-Qualification and Re-Validation activities pertaining to Manufacturing facility at Dholka site in line with the cGMP requirements of national
Execute day-to-day production activities for sterile injectable products as per approved production schedules. Perform and supervise manufacturing activities such as solution preparation, filtratio
Timely validation of all instruments in laboratory. All documents required for Regulatory compliance are maintained properly. To report any OOS/incidents/deviation discrepancy in laboratory analyst to
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
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
Principal Tasks: To analyse finished goods, semi-finish and In-process samples. Analytical result recording in LIMS and SAP. Specification, Master, Record of Analysis preparation/correction in LIMS
Plan, execute, and monitor daily granulation activities as per the approved production schedule. Supervise dispensing-to-granulation activities, including sifting, dry mixing, wet granulation, dryi
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