• Prepare plans, procedure & mechanism for laboratory manual & testing.• Establish inspection protocols, define sampling procedures, and determine equipment to be used in the testing process.• Verify the comprehensiveness of the tests as well as compliance of supporting documents, and ensure follow-up of abnormalities.• Provide support & guidance to QC staff for following GMP compliances.• Prepare & implement plans for the use of operational manuals (SOP) for laboratories.• Assist in formulating or revising quality control policies & procedures.• Identify abnormalities and determine the cause along with establishing corrective and preventive actions by ensuring follow-up.• Ensure laboratories standard & safety as per the local and international specification.• Communicate testing priorities and distribute work assignments to staff.• Coordinate with production department & other divisions according to the approved product plan & recommend necessary application to control quality at all stages.• Assist management in assessing and responding to product related complaints, investigations/deviations and in the preparation of annual product reviews.• Perform data review/auditing of analytical results produced by laboratory• Provide support to quality event management such as deviation control, CAPA managing, change control etc.• Prepare automatic & routine reports on laboratory mechanism & recommend necessary steps to develop performance.• Keep abreast on material handling such as raw material, packaging material, R&D samples & manufacturing samples.• •

Perform and document testing of pharmaceutical actives, excipients; intermediates and finished products (Tablets & Capsule & Oral suspension &Eye Drops) using instrumental analysis.• Prepares and standardizes volumetric solutions, reagents and indicators.• Analysis of stability samples including their related substances.• Making stability indicating Methods & Making Forced degradation Methods For different forms of pharmaceutical products