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This is a site-based, individual contributor position reporting to the Plant Engineering Manager at our new GMP Manufacturing facility in Clayton, Melbourne. As an Electrical Engineer, you will lead the execution, coordination, and compliance of all electrical-related work across GMP and non-GMP process and support systems. You will be a key first responder for troubleshooting and resolving electrical equipment issues—either hands-on or by managing external service providers. Your work will ensure compliance, safety, and operational readiness of Moderna’s state-of-the-art manufacturing operations in Australia.
Job Responsibility:
Supervising and coordinating routine and non-routine electrical work orders through the computerized maintenance management system
Coordinating specification, fabrication, procurement, installation, and engineering start-up of new equipment and systems
Leading remediation efforts for follow-up and emergency work related to deviations and corrective actions
Acting as the electrical subject matter expert supporting deviation investigations and CAPA
Developing and maintaining electrical procedures, safe work methods, and approved practices
Ensuring all electrical work meets EHS requirements including LOTO, hot works, and working at heights
Participating in a reliability-centered electrical program, including budget planning, spare part recommendations, and tracking quality metrics
Supporting internal and external audits with full compliance to cGMP and documentation practices
Supervising and developing site electrical standards and ensuring their compliance
Maintaining both electronic and paper-based cGMP records
Providing rotating “on-call” support for 24/7 plant operations and rapid response to site electrical issues
Maintaining Qualified Trainer certification to deliver On-Job Training (OJT) to colleagues
Performing other duties as required to support operational continuity
Requirements:
Trade qualification – A Grade Electrical License
Bachelor of Engineering (Electrical or equivalent) will be considered pending hands-on experience
3 to 5 years relevant experience working in a regulated (cGMP preferred) environment
Experience working in sterile manufacturing is highly desirable
Demonstrated management and proficiency in maintaining, and troubleshooting a variety of electrical supply and distribution, sensor’s, instrumentation, pneumatics, and drive systems used in bio-pharmaceutical production
Advanced control systems experience troubleshooting PLC’s, HMI/SCADA systems, Drives (VSD/Servo’s) and instrumentation
Advanced understanding of Good Manufacturing Practices (GMP)
Familiarity with GMP standards, quality management system processes and regulatory standards
Demonstrated understanding and management of regulatory requirements (TGA, FDA, EMA etc.)
Understanding of how to validate equipment and systems to ensure they are working as intended
Knowledge of electrical safety practices in the pharmaceutical industry, including handling of hazardous materials and electrical safety
Computerized Maintenance Management Systems (CMMS) experience to schedule and track maintenance activities
Excellent interpersonal and communication skills (verbal and written)
Ability to present own work to peers and cross-functional managers and influence leadership decisions
Technical writing skills required
Must have a customer service mindset
Ability to manage competing priorities is critical
Must be able use his/her technical background to investigate issues using a structured problem solving approach to determine true root cause and develop effective corrective and preventative actions
Must be able to find true root cause and path forward for complex problems
Ability to identify and drive improvements to electrical tasks and strategy
Demonstrated ability to learn new equipment/systems
Familiarity with Excel, Word, and PowerPoint are required
Ability to interact well with other groups and must be able to take ownership of and follow through on assignments
Must be able to drive results on multiple complex assignments simultaneously with minimal required direction from his/her supervisor
Ability to represent Moderna’s interests, objectives and policies in a professional and responsible manner
Nice to have:
Experience working in sterile manufacturing is highly desirable
What we offer:
Best-in-class healthcare
Voluntary benefit programs
Access to fitness, mindfulness, and mental health support
Family building benefits, including fertility, adoption, and surrogacy support
Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
Savings and investments to help you plan for the future