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EA Licence: 11C3793

Maintenance Engineer (Pharmaceutical/ Tuas)
Responsibilities
• Work as maintenance front line leader supporting production equipment reliability
• Ensure equipment availability for delivery of a reliable supply of products to customers
• Identify and drive continuous improvement initiatives to improve department and site business performance
• Carry out implementation activities for plant change control /modifications, capital projects and other identified plant improvement projects in line with defined specifications, budget and qualification of facilities in accordance with site to approved procedures.
• Provide engineering assessment, engineering design, plant troubleshooting and equipment failure root cause analysis
• Provides specialist advice to other departments and subordinates for trouble shooting / continuous improvements to processes / systems
• Provide input to the project team of capital projects as well as develop and implement the maintenance plan for newly installed equipment
• Provide site inputs to the development of Global Engineering Standards (GES) and Standard Engineering Practices (SEP)
• Monitor and enforce compliance measures (including safety) within their specific discipline to ensure inspection readiness of plant, as well as participate as an audit team member in the conduct of audits
• Supervise, develop, and motivate junior staff to help realize their maximum potential so as to contribute towards achieving the objectives of the department.
• Contribute to the development of the annual operating budget of the section to ensure achievement operational targets of section
• Responsible for planning and implementing plant maintenance, managing of engineering resources during plant turnaround and prompt resolution of breakdowns, including engaging external assistance.
• To support the development of facility master plan to ensure compliance to engineering standards, management of obsolescence and asset replacement.
• To support customer complaints and deviation investigations and ensure that all relevant engineering corrective actions are completed within the agreed timeline
• Prepare and issue Engineering Technical Report and provide input to Periodic Reviews and Annual Validation Report to ensure timely completion of the report.
• Maintain inspection readiness of the systems to ensure audit compliance with regulatory, safety and engineering standards
• Play a key role in all internal and external audits

Requirements:
• A good degree in Mechanical Engineering from a recognized university
• At least 5 years of relevant work experience in the pharmaceutical, petrochemical, chemical or relevant GMP process industry
• Knowledge of industrial standards (ASME; BS) and local codes
• Must be willing to provide support after office hours when required
• Good knowledge of cGMP and facility validation for the pharmaceutical industry will be an advantage
• Knowledge of machinery vibration, reliability analysis, instrumentation will be an advantage
To apply, please visit to www.gmprecruit.com and search for Job Reference: 12480
To find out more about this opportunity, please contact Lionel Liew at lionel.liew@gmprecruit.com.
GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Lionel Liew | Registration No: R1330693
   

Sounds like a good fit?

If you are interested in or qualify for this position, please visit our website at www.gmprecruit.com to submit your application now. You may also click on the Quick Apply (pencil) icon at the bottom of this page.

Because we strongly believe in fair employment, we practice objective merit-based consideration for all qualified applicants. If you are shortlisted for the position, you will hear from our friendly consultants personally.


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