Indoco Remedies

Expertise in Stability studies of pharmaceutical products, Analytical Method Validation, Analytical Method transfer for finished dosage forms.

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

Experience of formulation plant and knowledge of GLP & GDP. Should have knowledge of Microbiological testing, Environmental monitoring, Water system analysis, HVAC validation, QMS

Hands-on experience with HPLC, GC, UV-Visible Spectroscopy and Dissolution tester. Proficient in Empower-3 software. Strong analytical and problem- solving skills.

Knowledge of microbiological testing, environmental monitoring, water system analysis, HVAC validation, QMS. Able to carry in-process checks, line-clearance, knowledge of track & trace system, issuance of protocols, logbooks, BMR & BPR

M.Pharm; Responsible for development and execution of complex injectable, suspension, emulsion, ophthalmic formulations solution, emulsion for regulated markets. Should be responsible for review of trials and stability data throughout product development.

Perform audits individually or for evaluation and approval of new sites identified for Contract Manufacturing Loan license, third party, generic business for global markets including Domestic, ROW, Latam, Regulated Markets and Generic Business.

Achieve sales targets and execute growth plans for East Africa. Develop and implement strategies to expand market share in the region. Identify and negotiate business partnerships in untapped territories.

Environment Monitoring, QMS, Routine and Non-Routine Analysis, PET, Sterility, BET and Water Testing. QMS, IPQA, AQA, Qualification, Process and Cleaning Validation, Aseptic Core Monitoring