2-3

Hetero is one of worlds leading producers of key Active Pharmaceutical Ingredients (APIs) and generic formulations with presence in 140+ countries and backed by 30 years of experience in the pharma sector

Handling QMS as per Regulatory requirements. Handling Deviations, CAPA, Change Controls, OOS investigations. Responsible to process internal quality audits.

BDR Group of companies has grown steadily and become a house-hold name in the pharmaceutical Industry over the last 15 years, in both domestic and international arenas

Strong understanding of formulation analytical method development. Working knowledge of ICH guidelines, SAP. and documentation systems.

Exposure to OSD Manufacturing operations like Granulation, Pellet coating, Compression, Coating, Capsules, Primary Packing

Experience into Literature Survey, Identification of route of synthesis, Process optimization with respect to cost & quality scale up, documentation & characterization.

Intas is one of the leading multinational pharmaceutical formulation development, manufacturing and marketing companies in the world.

Person should have the worked on Peptide Manufacturing & Peptide Synthesis and Exposure to Peptide Synthesis, purification, filtration and drying processes and Peptides synthesis, Peptide purification, Lyophilization.

RPG LIFE SCIENCES LIMITED, ARE INVITING CANDIDATURE FROM PROFESSIONALS FOR BELOW MENTIONED POSITIONS