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EA Licence: 11C3793

Production Supervisor (Graveyard Shift/ Biomedical/ East)
Responsibilities
• Coordinate daily production floor activities and delegate assignments to production personnel
• Manage and motivate direct reporting employees by communicating job expectations, planning, monitoring and appraising job results; initiating, coordinating and enforcing systems, policies and procedures
• Develop and maintain training programs to ensure that all personnel have the necessary skills to perform their duties safely and productively; and to ensure that training skills are met for current and future demands of the shift
• Monitor and enforce working time, break, attendance, absence and leave planning of the production floor personnel
• Assist in the selection and training of direct reporting employees
• Monitor, measure and report on production related process performance and general issues
• To ensure good communication of clear expectations to production personnel, develop personnel growth opportunities and monitor employee work performance
• Maintain material and work flow throughout the manufacturing facility and ensure the workstations are supplied with material quickly and efficiently
• Ensure equipment and tools are in good working order and available for use when required
• To ensure that Health and Safety rules and regulations are adhered to during the shift and all matters relating to this are dealt with using the resources within the company
• Maintain compliance with established company’s policies and procedures
• Address problems and provide solutions to resolve the issues
• Maintain housekeeping standards to ensure a clean and safe work environment at all times by educating and directing personnel.
• To ensure company’s resources are used in an effective manner to achieve best operating costs
• Be able to make appropriate decisions while following company’s policies and procedures

Requirements
• Bachelor’s Degree in Engineering, Manufacturing, Business Administration or equivalent.
• 5 to 10 years of relevant working experiences in the medical device technology or pharmaceutical industry with minimum 3 years in managerial or supervisory capacity in a manufacturing environment.
• Experience working in a clean room environment will be advantageous.
• Good understanding of production and manufacturing processes and techniques.
• Basic knowledge of Six Sigma will be advantageous.
• Familiar with ISO13485 and GMP.
• Proficient in SAP and MES.
To apply, please visit to www.gmprecruit.com, job code: 16124.
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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