About the role
- Preparation of SOP as per standard format & preparation of the procedures as recommended by superiors.
- To maintain issuance, distribution and retrieval record of SOPs.
- Preparation of SOP index.
- To prepare job description.
- Assist in all documents preparation of QA.
- To carry out activities in the quantum software as per user rights.
- Monitoring of training activity in entire plant as per scheduler.
- Maintenance of following files: Masters, control and obsolete files of SOP’s and job description.
- To prepare self-inspection plan.
- Responsible for withdrawal of stability samples of finished product and submission to QC for analysis.
- To prepare stability protocol & stability report.
- Responsible for investigation of change control.
- Responsible for control sample set up, to maintain its withdrawal, destruction record and all logbooks.
- Responsible for monitoring temperature, relative humidity, pressure differential and calibration of thermo-hygrometer.
- To prepare risk assessment.
- To ensure online documentation.
- To carry out activities in the quantum software as per user rights.
Pedigree
B.Pharm / M.Pharm with 1-3 years of relevant work experience