Position Description

Production Supervisor (Perm Night Shift) / Medical Device (EAST)
Job Code 15457
Division GMP TECHNOLOGIES (S) PTE LTD (EA Licence:11C3793)
Job Placement Location Singapore
Apply Now

Jobscope:

  • 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

 

Requirements:

  • 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.
  • Strong intercultural experience and excellent interpersonal skills.

We regret that only shortlisted candidates will be notified.
GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Fiona Koh | Registration No: R1109239


 

Contact Person: Koh, Fiona - Reg No:R1109239 (fiona.koh@gmprecruit.com)

Back Apply Now