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 on line in-process checks as per SOP. To perform area cleaning as per SOP and maintain records. To perform cleaning and operation of Equipment's installed in parenteral manufacturing area. To perform routing activity as per routine and production plan. To perform all routine activity of autoclave. To perform filter integrity of hydrophilic/hydrophobic and disk filters as per routine activity. To perform proper status labeling of area and equipment as per SOP. To check monthly schedule of all measuring instruments and inform to supervisor. To record TEMP/RH in the parenteral manufacturing area. To take part in equipment qualification activities. 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 carry out the operation, documentation, and surveillance of equipment installed in parenteral manufacturing area. To handle additional responsibility assigned by HOD.
