Experience summary:
Ø Working as an analyst in DIVI’S & SYMED laboratories Sept-2016 to Till Date. It is an API & intermediate manufacturing unit approved by US FDA & EU GMP.
Ø Experienced Four US FDA and EU GMP audits during this period of working.
Job responsibilities:
Ø Sampling and analysis of cleaning validation samples using UV spectrophotometer, & HPLC.
Ø Performed analysis of stability studies samples by HPLC technique.
Ø Analysis of Final /finished product by HPLC technique.
Ø Perform analytical method validation by UV ,IR,POLARIMATER & HPLC technique.
Ø Very familiar with Empower software and LIMS.
Quality control tests