M.Sc

As Regulatory Professional II, the candidate will be responsible for making the timely submissions to the Health Authorities worldwide. The candidate is expected to establish and maintain the CMC part of the core regulatory file. 

Candidates with laboratory experience in human cell culture, animal handling and prior knowledge of developing therapeutics for different infectious and non-communicable diseases will be preferred 

Genome-wide evaluation of host genetic variations that associate with high risk for neonatal sepsis and sepsis related mortality. PhD in any branch Life Sciences from a recognized University. OR M.Sc or equivalent degree in any branch of Life Sciences from a recognized University

M.Sc. in Botany / Biochemistry / Plant Sciences / Biotechnology. Experience in molecular biology or genome editing techniques.

Successfully launch assigned brands in a specialty segment in line with brand strategy. Plan and consistently achieve patients on therapy, unit targets and value targets. B.Pharm / M.Pharm / M.Sc. candidates preferred.

Analytical Method Development, Method Validation, Analysis, HPLC, Stability, RM,GC, IP/FP

Competent in Process Validation, Hold Time Study, Cleaning Validation, and overseeing Validation Planner, with understanding of CSV and PLC validation

Encapsulation/ Gelatin, Medicament - Manufacturing Primary Packing, Compression and Coating , Granulation and Capsule Filling , Packing

Participate in function-specific sub teams and fulfill assigned project tasks and responsibilities under supervision -Uses professional concepts and company's policies and procedures to solve a wide range of difficult problems in imaginative and practical ways.