QC

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

Interview for M.Pharm, B.Pharm, M.Sc, B.Sc ; Stability, HPLC, GC, Wet Analysis, Dissolution, IP/FP, RM, LIMS, Microbiology.

Rusan is a research driven pharmaceutical company having its Manufacturing Units in India and Worldwide Marketing of Pharmaceutical Formulation, Active Pharmaceutical Ingredients and Intermediates.

Experience of HPLC, UV spectrophotometer, Walk-in Stability chamber and Dissolution Tester operation. Experience of Analytical Method Validation.

Ensure compliance of online documentation and line clearance activities. Review and approve executed BMRs/BPRs, logbooks, and related records.

Responsible for ensuring the quality of incoming material in process & finished products to ensure compliance with regulatory & standard specifications.

Analysis of RM / IP / FP samples, Operation and troubleshooting of instruments such as HPLC, UV, KF, IR, and Dissolution Apparatus.

Titan, an integrated Pharmaceutical Group which is backed by the holistic approach towards catering multifarious integrated services, which aims to meet the concept-to-commercialization needs of our customers while providing quality pharma and API products that serve for life saving medications.

Responsible for performing the chemical and instrumentation analysis for In-process, raw materials, packing materials, intermediates and finished products to meet the dispatch timeline as per the monthly schedule received from PPIC.