Chennai, Tamil Nadu 1-3 Yrs ₹1.5 - ₹05 Yearly
Job description
Roles Responsibility:
To execute
Pre-formulation studies, bench scale batches using different formulation
processes.
To support and
execute the tech transfer activities, pilot batch manufacturing and
bioequivalence studies etc.
Coordination and
correspondence for the arrangement of API, RLD, Excipients, Punches and other
accessories for Lab scale batches.
Coordination with
cross functional departments like RA, QA, QC and ARD.
Should have
knowledge of Solid oral and liquid oral dosage form development.
Should have good
knowledge of F RD equipment and their handling.
Responsible for
conducting Literature search, Experimental batches, Pilot and Pivotal batches.
Should have
exposure in patents and non-infringing development.
Must be able to
prepare development documents like Master Formula Records (MFR/MPR),
development protocols, and pharmaceutical development report.
Need to be develop
the Products by QbD fashion and expertise in DoE studies and interpretation
using competent software.
Willingness and
Cooperation to work at Contract Manufacturing Organization (CMO) sites.