To work as per cGMP and ensure its compliance as per current guideline and SOPs.
Independently handling of HPLC, GC & Ion Chromatography instruments with other analytical instruments for the execution of Method validation activity.
Require good analytical hand to perform the routine chemical test like Assay by titrimetric, KF, Clarity ,UV analysis etc. as per SOP/Pharmacopeia methodology.
Need sound knowledge for Method development related activity for Liquid and Gas chromatography by using sophisticated instruments.
Responsible to understand any non-compliance/event occur during execution of GMP activities.
Sound knowledge of EMPOWER, Chromele\xc3\xb3n, Agilent software etc. for operation of highly sophisticated analytical instruments.
Good documentation, Data recording and understanding regarding it\'s compliance for GMP and developement activity.
Instrument calibrations activity
Awareness for trouble shooting at the time of analysis.
Basic knowledge of MS office (Word, Excel & Power point)