Cadila Pharma

•	To plan and provide the analysis support as per approved specification & test procedure and standard operating procedures.
•	Ensure that, all the analysis as per customer specification is done (for dispatch) as per the planning (planning to be taken as per delivery instruction).  To review and monitor daily activity of dispatches and report to Quality Control Head 
•	To approve/reject raw material/packing material based on the analysis data.
•	To approve / reject the intermediate and finished product based on the analysis data. 
•	Review and approval of certificate of analysis for raw material, packing materials, intermediates and APIs.
•	To plan for Joint analysis with R& D personnel during analytical method transfer on HPLC/GC.
•	To review the supplement specification as per customer requirement.
•	To plan for analyst qualification activities and impart on job training to all subordinates.
•	To ensure the qualification/preventive maintenance and calibration has been followed as per approved scheduled and records maintained.
•	Ensure CFR-21 –Part 11 practices are followed effectively with online documentation and periodic review of audit trials for the computerized system / instruments.
•	To impart training as per cGMP, GLP, ISO system, Instrumental and technical training to all the concern staff. 
•	Authorized person for HOD review and impact assessment of Change control, CAPA, Deviation, OOS and OOT in LIMS.
•	To maintain and adherence of the GLP and safety procedures in laboratory.

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