1.Execute formulation development for new / generic dosage forms.
2.Conduct API, excipient and patent research for non-infringing formulation.
3.Perform stability studies as per ICH guildelines to ensure product quality.
4.Prepare SOPs, report and documentation in compliance with GMP
5.Coordinate with AR&Ds;, QA and manufacturing for tech transfer and scale up.
Preferred candidate profile
Basic understanding of pharmaceutical process and cGMP, with proficiency in Ms. office, robust problem solving ability, adaptability, project management skill and effective communication.