Indoco Remedies

Conduct cycle meetings, sales training & drive SFE initiatives. Collaborate with cross-functional teams for successful product launches.

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