<ul><li>Experience in review of HPLC, GC and other chromatography systems (Preferred faced regulatory audit like USFDA/ MHRA/TGA).</li><li>Responsible for Preparation and Review of Analytical method development and validation.&nbsp;</li><li>To guide team members for cost effective method development.</li><li>To monitor the execution of R&amp;D samples, stability samples, raw materials and excipients received from contract giver.</li><li>To provide job training and related advance topics as and when it require.</li><li>Responsible for execution and approval of Analytical Instrument Qualification and Calibration Responsible for preparation, review and approval of STP, SOP, Protocol and its reports.</li><li>Responsible to ensure all quality related issues are handling as per respective SOP, Investigation to identify root.</li><li>Cause or most probable root cause and appropriate CAFA Initiate to avoid reoccurrence of the same.</li><li>Responsible to maintain and follow GLP and GOP in compliance manner in laboratory.</li></ul>

Assistant Manager-ADL