Cadila Pharma

•	Responsible for all activities related to raw material and packaging material of main pharma QC at Dholka plant.
•	To ensure current good laboratory compliances and ensuring all SOPs related to quality control laboratory are prepared and reviewed / implemented properly.
•	To manage an accurate, reliable, efficient and timely testing function of vendor samples, raw material and packaging material.
•	To ensure that the persons are working in the laboratory with proper compliance and follow the GMP & ALCOA+ Principle norms.
•	To ensure timely release of Vendor samples , raw material and Packing Material in order to avoid delay in delivery of goods.
•	To ensure timely regulatory & audit compliance related to raw material and Packing Material along with effectiveness. 
•	To ensure that only trained & Qualified and authorized personnel are in working on respective working area. To carry out review and suggest periodic training, wherever required.
•	To investigate and file change control, deviation, out of Specification (OOS), out of trend (OOT) report and Laboratory incidence whenever observed.
•	To ensure timely closer of QMS related to raw material and Packing Material along with root cause and CAPA. 
•	To review the Specification/STP and to update them from time to time if required.
•	To communicate the regulatory, technical and quality information to all the concerned.
•	To ensure the timely sampling of raw material and  packaging material as per requirement .
•	To ensure the training about the changes in the standard operating procedure (SOP) if required.
•	To ensure accurate document preparation / review procedures being carried out relating to raw material and Packing Material as per the regulatory norms, checking / monitoring them and review and approve certificate of analysis .
•	To initiate, review and implement the change control wherever necessary after getting it approved from HOD.
•	To review and update the specifications as per pharmacopoeia and other regulatory requirements.
•	Participation in quality review team.
•	Any other work assigned by HOD.

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