Analytical Chemist

Core Purpose of the Role:

This role involves method development, method validation, method transfer and R&D stability studies by using laboratory instruments like Ultra performance liquid chromatography (UPLC), High Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Ultraviolet (UV) spectrophotometer, Polarimeter, etc. 

Role Accountabilities:

•     Must have strong hands-on experience in development and validation of Assay & related substances methods for drug substance/drug product. Managing the stability studies for individual projects and stability data analysis, knowledge on stability guidelines and maintaining the sample storage.
  •    Must have experience in handling HPLC, UPLC (Empower-3 software), GC, UV Visible spectrophotometer balances, Potentiometer, and stability chambers•    Shall have experience on Good documentation/laboratory practices such as ALCOA+ 
•     Experience in calibration and qualification of HPLC, UPLC, GC, and other QC laboratory instruments
  •    Shall prepare and review the raw data sheets, instrument operating procedures, and standard operating procedures•    Shall have good experience in handling of QMS (such as incidents, Out of Specifications, Deviations, and Change control) 
•     Shall be responsible for procurement and inventory maintenance of Pharmacopeial Standards/Chemicals/Reagents/Consumables/Spares etc., required for the projects
  •    Shall adhere to the procedure of GxP/Safety and as per the procedure defined in the internal standard operation procedure•    Shall operate the MS office (word, excel, ppt), outlook, and other essential tools required for routine activity•    Good communication and e-mail writing skills are required since the candidate needs to communicate to client/external users situated overseas