Responsibilities
- Follow GMP (Good Manufacturing Practices)
- Understand and comply with GMP requirements during all manufacturing activities.
- Learn why compliance is critical for patient safety.
- Read and Follow SOPs
- Study Standard Operating Procedures before performing any activity.
- Learn how manufacturing processes are standardized and controlled.
- Observe Manufacturing Operations
- Gain exposure to dispensing, granulation, blending, filling, packaging, or biologics manufacturing processes (depending on the facility).
- Maintain Production Documentation
- Support batch records, logbooks, and manufacturing documentation.
- Learn Good Documentation Practices (GDP).
- Monitor Shop Floor Activities
- Participate in daily production reviews and understand workflow management.
- Learn Equipment Operations
- Observe equipment setup, operation, cleaning, and maintenance activities.
- Understand the importance of qualified equipment.
- Support Line Clearance Activities
- Learn how production areas are checked before starting a new batch to prevent mix-ups.
- Participate in Safety and EHS Activities
- Follow safety procedures, PPE requirements, and emergency response processes.
- Understand Deviation Reporting
- Learn how manufacturing issues, deviations, and incidents are documented and investigated.
- Assist in Production Data Analysis
- Support collection and review of manufacturing metrics such as yield, downtime, and productivity.
- Learn Cross-Functional Coordination
- Work with Quality, Warehouse, Engineering, Planning, and Supply Chain teams.
- Understand how departments collaborate to deliver products.
- Participate in Continuous Improvement Projects
- Contribute to Lean Manufacturing, 5S, Kaizen, process optimization, or productivity improvement initiatives.
Qualifications
- B PHARM, BSc (Chemistry)
- Duration: 1 year
- Pass Out Batch: 2025, 2026
Eligible Candidates Please send their CV to the Below.
Email ID : [Confidential Information]
