Job Purpose

To ensure the reliable operation, monitoring, and maintenance of pharmaceutical production and laboratory process equipment, including water systems, utilities, and supporting facilities, while upholding cGMP, GDP, and EHS standards. The role safeguards product quality, minimizes equipment downtime, and contributes to the continuous improvement of engineering systems and compliance.

Key Responsibilities

1. Operations & Monitoring

• Operate and monitor water systems, production equipment, laboratory instruments, utilities, HVAC, BMS, EMS, and associated control systems.

• Detect and escalate abnormalities to prevent disruption of production and quality processes.

2. Maintenance Execution

• Perform preventive, corrective, and breakdown maintenance to ensure optimal equipment performance and minimize downtime.

• Troubleshoot technical issues and restore systems within defined response timelines.

3. Calibration & Testing

• Conduct calibration, verification, and testing of instruments, alarms, and control systems in compliance with cGMP and regulatory standards.

• Maintain calibration records and support audit readiness.

4. Documentation & Compliance

• Maintain accurate engineering documentation in line with cGMP, GDP, and regulatory requirements.

• Ensure timely completion of work orders, logbooks, and reports.

5. EHS Compliance

• Adhere to all Environmental, Health, and Safety (EHS) procedures, including statutory inspections, waste management, and safe work practices.

• Support incident reporting, risk assessments, and corrective actions.

6. Facility & Vendor Support

• Assist in managing utilities, facility systems, and AMC (Annual Maintenance Contracts).

• Coordinate with external vendors and contractors to ensure smooth service execution.

Department: Engineering
Experience Required: Minimum 3 years
Education: Diploma in Engineering (Electrical, Mechanical, Electromechanics, or similar)
Languages: English