M. Pharm / B. Pharm / M. Sc
Experience : 3 to 10 years
Should have experience in Stability Analysis; handling HPLC / GC; Analysis of raw materials, finished products, in process samples and oral suspensions by HPLC
Must have good knowledge in GLP
Must be experienced in analytical methods development, methods validation and tech-transfers to QC for raw materials, intermediates and finished products.
Should be able to conduct routine analysis of finished product and innovator samples.
Should be well versed in ICH guidelines and different regulatory authorities