Team member - Drug Substance - Cell Banking

About the role

We are looking for an individual to execute downstream/upstream manufacturing unit operations, ensuring documentation and compliance within GMP (Good Manufacturing Practices), regulatory, and organizational guidelines. The objective is to produce products within defined volumes and timelines while maintaining compliance with quality standards, GMP, and other regulatory and statutory requirements, as per the schedule.

What you'll do

• Execute unit operations within Upstream according to the BPR (Batch Production Record), conduct activities to support production schedules
• Perform routine process area cleaning, autoclave operation, manual cleaning and sterilization of components and parts, monitoring processes and results
• Issue discrepancies, collaborate with cross-functional departments to close them, implement corrective actions, and comply with GMP and safety standards
• Complete batch documentation in alignment with GMP, ensuring data collection and maintenance meet cGMPs (Current GMP), company standards, policies
• Emphasizing safety awareness and continuous improvement, you will actively adhere to safety rules and promptly report unsafe matters and near misses/accidents

What you need

• 3–6 yrs of experience
• GMP
• Documentation
• Calibration
• Communication
• B.Tech or B.E.