Maintain reliable operation of electrical, instrument, Building Management System (BMS), Non GMP equipment.
Partner with shift utility personnel to perform daily site walk down, logging, sample collection and analysis.
Monitor utility system performance in BMS and Delta-V and partner with shift utility personnel to respond to alarm.
Apply technical knowledge and hands-on support to carry out troubleshooting of equipment breakdown or failure relating to electrical, instrument, BMS and non-GMP equipment.
Involve and support maintenance of electrical, instrument and non-GMP including plant shutdown maintenance.
Report abnormality or emergency issue to engineer, line manager or stakeholder. Support to conduct basic frontline troubleshooting / investigation to resolve problem or abnormality.
Support engineer or in-line manager to do deviation investigation using Fishbone Ishikawa or 5-why diagram.
Involve in data gathering and support engineer or in-line manager to create spare parts and consumables in Maximo.
Support planning and communicating with stakeholders/vendors for the execution of maintenance or project or repair work in compliance with safety and quality requirements.
Partner with SEM (Calibration, HVAC, Clean Utilities, Process Engineering, Validation, shift utilities) and project teams for excellent execution of maintenance, projects, or troubleshooting-related work.
Proactive and able to work with minimal guidance in day-to-day or maintenance work.
Preferred Qualifications
NITEC or equivalent technical school or Diploma certification in Mechanical, Electrical, Automation, or Pharmaceutical Engineering, candidates with equivalent work experience is plus. Equivalent work experience in the pharmaceutical industry, GMP environment, or oil & gas industry is a plus.
Ability to learn quickly, applying engineering knowledge and relevant skills to translate/simplify them into actionable steps.
Demonstrate good communication and presentation skills and comprehension abilities.
Display a good working attitude, strong work ethic, and willingness to follow leadership directives.
Open to accepting temporary work assignments, including overtime on weekends or weekdays, and other roles as required.
Excellent verbal and written communication skills in English.
Career development
With complete systematic training, you can potentially become a shift lead and a subject matter expert in your respective discipline.
A performance-oriented promotion system, diverse and comprehensive challenges in a cGMP manufacturing environment, and career advancement incentives will all contribute to your career development.
Explore your management potential and grow with the team in the Antibody Drug Conjugates industry of the future.
