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
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.
Candidates must knowledge on all areas of production activities. Like handling of GLR, SSR, Centrifuge, Driers, Blender, Shifter, Miler, Documentation review, and regulatory knowledge.
Bharat Parenterals Ltd. is a Gujarat based pharmaceutical company, established in 1992 by Mr. Ramesh Desai, who started the company with a vision of making world class affordable medicines and to take it to the forefront of contract manufacturing units in Gujarat.
To monitor & prior checkup of equipment planned for usage in Scale up, Exhibit, Process validation batches i.e. Equipment preparation, vial washing and dehydrogenation, CIP, SIP System, PLCs, instruments etc.