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Senior Maintenance Technician (GMP)

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Original
Simplified
Senior Maintenance Technician (GMP)
Job ID
193079
Posted
02-Dec-2024
Service line
GWS Segment
Role type
Full-time
Areas of Interest

Building Management, Engineering/Maintenance, Facilities Management

Location(s)

Johor Bahru - Johor - Malaysia, Singapore - Singapore

About the Role:

As a CBRE Maintenance Sr. Technician, you will be responsible for supporting sitewide routine operation and maintenance and ad hoc corrective maintenance to process equipment, utilities and facilities system.

This role will be required to support equipment / instrument calibration and performance. All the tasks need to be done in compliance with cGMP, EHS, Data Integrity, and regulatory requirement.

What You'll Do:
  • Participate in problem solving discussions with cross functional team to identify / define and root cause, evaluate alternative solutions, and develop action plans.
  • Execute the routine maintenance for the site utilities systems, production equipment, control systems, etc in a timely manner and in compliance with engineering standards and safety procedures.
  • Complete training provided on-time to improve competencies.
  • Contribute to team effort by accomplishing desired results/KPIs. Share knowledge and coach colleagues to build-up their competencies.
  • Manage third-party vendor who is contracted to perform routine preventive maintenance, corrective maintenance and any other maintenance related activity.
  • All GMP documentation related to maintenance activities is completed accurately and processed to full completion in compliance to data integrity requirement.
  • This job involves working different shifts (Morning and Night) on a rotating basis and may include weekends and holidays.
  • Candidates must have experience working in a pharmaceutical plant.
  • Carry out any other duties and responsibilities as assigned by supervisor, including but not limited to the above.
What You'll Need:
  • NITEC or Diploma in Engineering related qualifications.
  • Minimum 5 years with relevant experiences in pharmaceutical industry.
  • Able to work in a fast pace and a regulated environment.
  • Strong understanding of facilities and utilities systems and process equipment related validation / GMP requirements.
  • Able to work in a fast pace and a regulated environment.
  • Able to plan, schedule, organize, prioritize day to day activity.
  • Strong troubleshooting skill and a good knowledge of different RCA tools.
  • Able to work independently.
  • Able to work rotating shift.
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