Indoco Remedies

Review of stability data. Review of analytical method validation data. Review of analytical method transfer.

Candidate should have thorough knowledge on regulatory guidance, literature search applicable for sterile formulation development.

Hands on Experience on, Stability Studies, Analytical Method Validation & Finished Goods.

Experience in granulation, compression, capsule & coating oral liquid manufacturing areas of regulated markets. FDA approved personnel in tablet manufacturing would be preferred.

Experience in environment monitoring, QMS, routine & non routine analysis, PET, sterility, BET & water testing.

Knowledge of handling HPLC, UV, Karl Fischer, Autotitrator, GC and dissolution in sterile and non-sterile.

Knowledge of handling compression machine Sejong / Cadmach machine / tooling SCADA based machine

Diploma / D.Pharm / BSC / B.Pharm / M.Pharm. Pharma Production, Quality, Microbiology at Indoco Remedies

Indoco Remedies Ltd., is a fully integrated, research-oriented pharma company engaged in the manufacturing and marketing of Formulations and Active Pharmaceutical Ingredients