Responsibilities
* 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 electrical 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.
Qualifications
* Bachelor of Engineering (Electrical or equivalent) is preferred.
* Trade qualification – A Grade Electrical Licence.
* 6 to 10 years of relevant experience working in a regulated (cGMP preferred) environment. Experience in sterile manufacturing is highly desirable.
* Demonstrated management and proficiency in maintaining and troubleshooting a variety of electrical supply and distribution, sensors, instrumentation, pneumatics, and drive systems used in biopharmaceutical production.
* Advanced control systems experience troubleshooting PLCs, HMIs/SCADA systems, VSDs/servos, 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) and technical writing skills.
* Customer‐service mindset and ability to manage competing priorities.
* Structured problem‐solving approach to determine root causes and develop effective corrective and preventative actions.
* Ability to identify and drive improvements to electrical tasks and strategy.
* Demonstrated ability to learn new equipment/systems.
* Familiarity with Excel, Word, and PowerPoint.
* Ability to interact well with other groups, take ownership of assignments, and follow through with minimal direction.
* Ability to represent Moderna's interests, objectives, and policies in a professional and responsible manner.
Requirements
* This position is site‐based, requiring full‐time presence at Moderna's site in Clayton, Melbourne.
* Remote work is not an option.
* The role may be subject to pre‐employment and periodic medical assessments in line with relevant legal and operational requirements.
Benefits
* Quality healthcare and insurance benefits.
* Lifestyle spending accounts.
* Free premium access to fitness, nutrition, and mindfulness classes.
* Family planning and adoption benefits.
* Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year‐end shutdown.
* Savings and investment programs.
* Location‐specific perks and extras.
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