Candidate should have very good educational and theoretical background.
Candidate should have knowledge of calibration, method development and troubleshooting using various instruments like KF auto titrator, dissolution (I, II & IV), spectroscopic instruments e.g. UV spectrometer, IR and Chromatographic instruments e.g. HPLC, GC
Knowledge of various regulatory guidelines w.r.t. method development, product development and documentation
Knowledge of method development for oral dosage forms w.r.t. tests like assay, degradation products, dissolutions, blend uniformity, content uniformity, cleaning method, etc.
Knowledge of specification setting for oral dosage forms, in-process specifications as well as product specifications
Knowledge and operating of instruments like LC-MS, GC-MS will be added advantage
Good understanding of Documentation as per GxP requirements
Online Lab note book writing
Method development report preparation - Assay, Degradation products, Dissolution, cleaning method, etc.
Method of Analysis, Test report, SOP preparation
Calibration documentation
Review of documents generated by peers or juniors
Should be able to search scientific literature on-line
Should be a team player and able to coach juniors technically