About the Organization :
The firm is more than 200 years of experience in producing the quality standards helping major bio-pharmaceutical firms in delivering high quality medicines to relieve many diseases. This is an organization supplying methods at free of cost for the product development and maintaining the standards. This is distributed across the globe serving mankind.
About the Job :
The Current position is a supervisory position for the updating of US pharmacopoeia NF monographs. The candidate need to handle the entire life cycle of work starting from procurement by lab request to execution and reporting. This position holds the responsibility of managing both drug substance and drug product portfolio.
Need to support with Scientific Liaison and QA team for flow of the work
Experience :
Masters with 12+ years of experience or PhD with 5-6 years of experience in pharmaceutical industry
Need to know the QBD approach of development
Exposure to instrumental techniques like UHPLC, GC-MS, ICP-MS, UV-Vis, FT_IR, LC-MS
Should have strong communication skills and writing skills
need to work flexible, some times out of office hours
Need to handle the IQ/OQ and PQ of instruments procured
Reviewing of the team dat for the compliance