Manufacturing Supervisor (Medical Device / East)

GMP TECHNOLOGIES (S) PTE LTD| Date Posted: 3-Nov-2019
EA Licence No: 09C3051|EA Personal Registration No: R1109239
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Job Nature:
Position Level:
Diploma, Bachelor's / Honours

Job Description


  • To take responsibility of the shift in terms of management of staff, management of production processes and quality targets
  • To ensure the smooth running of the production processes and maintain a positive work atmosphere
  • To take responsibility of the quality and product that is produced within the shift in line with company’s quality systems, processes and procedures
  • 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
  • Monitor, measure and report on production related process performance and general issues
  • 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
  • Address problems and provide solutions to resolve the issues
  • To have an active role in company’s continuous improvement plan to achieve plans for future growth within the company
  • Maintain housekeeping standards to ensure a clean and safe work environment at all times by educating and directing personnel


  • Bachelor’s Degree in Engineering, Manufacturing, Business Administration or equivalent.
  • Continuing education in Production Management will be preferred. 
  • Min. 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 help us process your application, please visit to upload your resume on our website.
GMP Technologies (S) Pte Ltd   |   EA Licence: 11C3793   |  Fiona Koh  |   Registration No: R11092398

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