Co-ordinate effectively with related department (Maintenance, Q.C, Store &R&D) for smooth running production schedule
*To insure work permit requirement are strictly followed after issuing work permit in plant area.
Handle Stability section & GLP section.
Preparing protocols, summary sheets in stability section.
Monitoring of temperature and humidity record in stability.
Maintaining withdraw record and all stability documents
Handle and maintain stock reference and working standards.
Preparing STP and SOP .
work as a planner and supervision in stability section.
Handle and maintain coloumns record in HPLC.
Review and checking of data in stability.
Troubleshooting in Hplc
Handling team in Hplc analysis (stability)
check all log books of instruments ,and working standards ,Referance standards.
calibration of all instruments in QC (Hplc, UV,FTIR,Dissolution etc)
Responsibilty
to handle incidence reports and documents
Test parameter of Assay, Related substances ,content uniformity, D.T, etc
Capability to test all type of samples chemical as well as instrument.
Take responsibilities on the absence of my senior
Reporting to the HOD QA & QC
Follow GLP and GMP
Capability to work all QC activities
Ensuring adherence to IS 13428:2005, ISO 9001:2008, 2005: 22000 and HACCP norms.
Consistent evaluation of vendor performance to ensure supply of quality material.
Preparing documentation as per ISO 9001:2008, 2005:22000, FSSAI, IP, HALAL.
Inspecting & maintaining quality standards for incoming packing & raw materials, ensuring stringent adherence to quality standards, norms & practices,identifying gaps and taking corrective action.
Ensuring delivery of tested, safe and quality product.
Mostly attention toIP, ISO, QMS, FSMS, HACCP,FSSAI, HALAL, maintain guidelines as per norms.
ISO 22000: 2005, ISO 9001: 2008, FDA, Quality & food Safety policy.