•To maintain proper hygienic condition before entering to parenteral manufacturing area. •To follow parenteral manufacturing area entry exit procedure properly. •To take part in training whenever necessary. •To perform the cleaning activity as per SOP. •To perform cleaning and operation of vial washing machine, Dehydrogenation tunnel and maintain the record. •To perform cleaning and operation of equipment installed in parenteral manufacturing area which ever is applicable •To perform on line in-process checks as per frequency. •To perform area cleaning as per SOP and maintain record. •To perform proper status labeling of area and equipment as per SOP. •To check calibration schedule of all measuring instruments and inform to supervisor. •To check integrity status of all equipment installed in parenteral manufacturing area and inform to supervisor. •To record TEMP/RH of parenteral manufacturing area. •To inform supervisor if any deviation from approved process. •To follow Good documentation practice during documentation. •To maintain area and equipment logs as per SOP. •To follow plant wise cGMP compliance. •To ensure Data integrity . •To handle additional responsibility assigned by HOD.
