Job Description
- To Perform the Manufacturing Activity as per the SOP.
- Operation, Cleaning, and maintenance of the compression Machines, Metal detector & deduster as per SOP.
- Calibration of the balances and other Instruments.
- Online recording of the activity in the BMR and Logbooks.
- Checking and recording of the in-process parameter during manufacturing activity.
- Troubleshooting of equipment by coordination with engineering department
- To ensure safety and hygiene during manufacturing processes.
- Follow the supervisor’s instructions to achieve departmental goal.
- To report any incident or violation of GMP act to immediate supervisor
- To carry out the activity in effective manner to achieve departmental objective.
- Exposure to external Audits- USFDA, MHRA, TGA, ANVISA etc.
·To maintain the c-GMP environment in Manufacturing area.
·Additional responsibility of Preventive & regular Maintenance of machine.
·Accessories and inventory control of the area.
·Monitoring productivity improvement.
·Monitoring change overtime reduction.
Qualifications & Pre-Requisites
- D. Pharm/ ITI
- Total experience of 5+ years in OSD formulation.
·Should have good experience in operation of Compression equipment – Cadmach, Korch, Sejong, Karnavati, Fette etc.
Additional notes- Role is expected to work in all shifts.