To perform the manufacturing activities as per the batch processing record,
To perform the disinfectant preparation, ensure and perform the area cleaning activities,
Responsible for batch calculation and check the dispensed materials.
To ensure and perform the CIP, SIP, filter integrity and batch preparation activities.
Responsible for the reconciliation of filled and sterilized bottles.
To keep all the equipment in working condition and check and monitor the scheduled PMP activities
Co-ordinate with other relevant department regarding manufacturing, sampling and other stages of the process as per the batch processing record.
Record deviations and discrepancies in the batch stages and report to the QA personnel and production manager.
Preparation of L.VP facility documents i.e. SOP, MFR, BMR and BPR.
Handling of QMS activities ie Incidents, Change control, Deviation and CAPA.
Actively participate in internal and external audits.
cGMP compliance and implementation of GMPs activities and ensure the Online documentation activities.
Responsible to achieve the monthly production targets and to support the operators and executives to achieve the monthly target goals.
Responsible for the LVP entire facility maintenance like man and material movement as per procedure and monitor the area and report to superiors about the non cGMP compliance activities.
