The Team Leader – Electronics Engineering & Automation is responsible for managing and supporting all electronic systems, automation equipment, and control systems within the solid dosage manufacturing and packaging lines. The role ensures reliable operation, regulatory compliance (GMP), minimal downtime, and continuous improvement of automated systems used in production and packaging processes.
The position leads a team of technicians and engineers to maintain, troubleshoot, optimize, and upgrade PLC, SCADA, HMI, and instrumentation systems supporting pharmaceutical operations.
Key Responsibilities
Automation & Control Systems
Supervise and maintain PLC, HMI, SCADA, and industrial control systems used in solid dosage manufacturing and packaging equipment.
Manage automation systems for equipment such as:
Tablet compression machines
Capsule filling machines
Blister packaging lines
Bottle filling and labeling lines
Checkweighers and serialization systems
Support troubleshooting and programming of PLC platforms (Siemens, Allen Bradley, etc.).
Maintain and optimize SCADA and data acquisition systems.
Maintenance & Troubleshooting
Lead preventive and corrective maintenance of automation, sensors, drives, and electronic systems.
Diagnose and resolve automation failures, control loop issues, and communication faults.
Ensure minimal production downtime through rapid technical support.
Team Leadership
Supervise and guide automation technicians and electronics engineers.
Plan daily maintenance activities and allocate resources.
Provide technical training and mentoring to team members.
Ensure adherence to safety procedures and GMP requirements.
Equipment Qualification & Validation
Support FAT, SAT, IQ, OQ, and PQ activities for new equipment.
Collaborate with QA, validation, and production teams during commissioning.
Ensure automation systems comply with GMP and 21 CFR Part 11 requirements where applicable.
Continuous Improvement
Identify opportunities for automation upgrades and process optimization.
Implement root cause analysis (RCA) and corrective actions for recurring issues.
Support digitalization and Industry 4.0 initiatives within manufacturing.
Documentation & Compliance
Maintain accurate maintenance records, SOPs, and change control documentation.
Ensure compliance with GMP, regulatory, and company standards.
Support internal and external regulatory audits.
Required Qualifications
Education
Bachelor’s Degree in:
Electronics Engineering
Electrical Engineering
Mechatronics Engineering
Automation Engineering
Experience
5–8 years’ experience in pharmaceutical manufacturing automation or industrial automation.
Experience with solid dosage manufacturing or packaging equipment is preferred.
Minimum 2–3 years in a supervisory or team leader role.
Technical Skills
PLC programming (Siemens S7, Allen Bradley, etc.)
SCADA systems
HMI configuration
Industrial communication protocols:
Modbus
Profibus
Ethernet/IP
VFDs and servo drives
Instrumentation and sensors
Troubleshooting of automated packaging lines
Understanding of GMP and pharmaceutical compliance
Soft Skills
Strong leadership and team management
Problem solving and analytical skills
Effective communication with cross-functional teams
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