To maintain strict adherence of GLP in the analytical development laboratory
To review and maintain IQ/OQ/PQ and scheduled calibration report of all instruments/equipments in the analytical development laboratory
To ensure the review of all analytical records for correctness, completeness and compliance to cGMP so as to facilitate sharing of documents with Contract Giver
To prepare SOP, Specification and Standard test procedure as per the requirement
To ensure that the changes in the current regulatory guidelines are implemented and evaluate them from time to time
To review daily verification records of instruments/equipments like balance, pH meter and Daily temperature monitoring in the laboratory.
To review C.O.A of working standard, finish product, stability compilation and other Quality documents as and when required.
Working with all members of staff to maintain and develop the positive progressive culture within the Laboratory.
Observing and complying with Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP)
To ensure that appropriate safety procedures are followed in the laboratory
To carry out any other work as assigned by Department Head/ Head - Quality