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
• ECRS 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.
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• Critical Exposures:

• Experience in performing calibration of calibration verification of manufacturing equipments.

Qualifications :

Educational Qualification

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

Work Experience:

3 to 6 years of experience.

Remote Work :

No

Employment Type :

Full-time