JOB RESPONSIBILITIES 1. Working on Unit operations related toupstream processing during Drug Substance (DS) manufacturing.
- GMP documentation related to DS manufacturing like batch records, equipment usage, facility monitoring.
- Preparation of documents like SOPs, MMDs and QMS related documents like change control, deviation, CAPA, risk assessment etc.
- Monitoring of manufacturing facility and keep it cGMP compliant 5. Involvement during regulatory audit preparation 6. Co-ordination with cross functional teams like QC, QA, Maintenance, Warehouse, Injection etc.
- Training and mentoring current joinees 8. Keep the track for calibration and qualification activities, for example for equipment, weighing scale and standards etc.
- Preparation and maintenance of virus stocks and cell banks
📌 Deputy Manager (Dholka)
🏢 DigiCAD
📍 Dholka
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