Team Member - Manufacturing (Liquid) - Operator

Role and responsibilities:

• You will be responsible for the operation, verification, calibration, and proper use of instruments in the Oral Liquid Manufacturing area.
• You will be responsible for machine setup, operation, and cleaning of all manufacturing equipment used in the Oral Liquid Manufacturing area.
• You will be responsible for performing and documenting in-process checks in accordance with approved BMRs and SOPs.
• You will be responsible for participating in troubleshooting activities to minimize operational risks and equipment downtime during breakdowns.
• You will be responsible for the operation, verification, calibration, and proper utilization of manufacturing equipment in the Oral Liquid Manufacturing area.
• You will be responsible for the execution, review, and recording of Electronic Batch Records (EBRs), e-logbooks, calibration and verification records, ECRs, and other related documents through PAS-X (Process Automation System).
• You will be responsible for the execution of CLITA activities and the logging, monitoring, and closure of Red Tags and White Tags in the AMPLE system.
• You will be responsible for reporting and recording Near Misses, Unsafe Acts, and Unsafe Conditions in the SHEHUB system.
• You will be responsible for reviewing and verifying SCADA/L2 batch reports to ensure accuracy, completeness, and compliance.
• You will be responsible for documentation activity like deviations, calibration, change control etc. related to manufacturing area
• You will be responsible for identifying process abnormalities, implementing lean tools such as 5S, Kaizen, and Autonomous Maintenance, and coordinating small project modifications with plant leads.

Skills & Attributes Functional Skills:

• Computer System operation
• Machine operation
• 5S maintaining
• MES operation
• ECR'S execution
• Technical Documentation
• Audit Management
• Compliance Management
• Lean Methodologies
• Root Cause Analysis
• Workplace Safety
• Behavioral Skills
• Proactive Safety Awareness – Demonstrates vigilance in identifying hazards and enforcing safety protocols during maintenance activities.
• Process Discipline and Documentation – Maintains accurate records, follows SOPs, and ensures compliance with GMP/cGMP and statutory standards.
• Collaborative Problem Solving – Works effectively with cross-functional teams to troubleshoot issues, implement solutions, and drive continuous improvement.
• Critical Exposures:

• Experience in performing calibration of calibration, verification of manufacturing equipment's.

Educational Qualification

Diploma/Graduation in pharmacy, Mechanical, Electrical, Instrumentation Engineering or related field is mandatory.

Work Experience:

3 to 6 years of experience.