Perform analysis of raw materials and finished products using UV, IR, HPLC, UPLC, GC, LCMS, etc. Ensure adherence to SOPs, GMP, and ALCOA principles during shift operations.
M.Pharm / MS Pharm / M.Tech. / M.Sc. with specialization in Medical Devices/ Biomedical Sciences/ Chemistry / Electronics / Biotechnology / Material Sciences / Nanoscience / Nanotechnology or equivalent.
Dossier & document preparation as per CTD, ACTD & country specific guidelines, Review of dossiers, DMF & Technical documents, Answer query raised from regulatory authority.