Key Responsibilities:
Perform chemical analysis of bulk and finished products (mainly Tablets).
Conduct weight variation tests during in-process and final stages.
Assist in stability studies using Dissolution & Disintegration apparatus.
Operate and calibrate UV-Spectrophotometer, Dissolution, and Disintegration test
machines.
Maintain log books, SOPs, and ensure regulatory documentation.
Prepare bulk and finished product reports.
Ideal Candidate:
B.Sc. / M.Sc. in Chemistry or related field.
Keen interest in pharmaceutical quality control.
Strong documentation habits and attention to detail.
Willing to learn and grow in a GMP-regulated environment.