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EA Licence: 11C3793

Production Supervisor (Medical Device Mfg) (MNC / East)
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. GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | Fiona Koh | Registration No: R1109239 Contact Person: Koh, Fiona - Reg No:R1109239 (fiona.koh@gmprecruit.com)    

Sounds like a good fit?

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