M.Pharmacy; Responsible for Formulation Development of Nasal Formulations. Responsible for conducting Formulation Development Trials and documenting the details in LNB.
RA publishing will participate in the publishing of different regulatory activities. The focus will be to ensure 100% quality and timeline of the submission. This role will be the primary interface with the Regulatory Affairs Associate
Knowledge of handling SCADA base coating machine. Knowledge of equipment in granulation and able to handle Integrated Granulation Line PLC based equipment
Responsible for Monitoring and Completion of the production batches as the scheduled timelines. Responsible for implementation of the cGMP practices in the area. Responsible for Indenting of the production process related accessories and consumables.
Supervise production team operations. Handle equipment: Sifter, FBD, Dryer, Centrifuge, ANF, Spray Dryer, Reactor, etc.
Ensure compliance with GMP processes. Maintain BMR, BPR, and logbooks.
Compounding, Filling, Vial Washing, Tunnel, Autoclave, Capping, and Packing activities. Disinfectant, MLT, BET, and sterility method validations, executions, and related documentation, Culture handling & EM monitoring.