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ResMedPosted 1 month ago

Supervisor, Manufacturing Technician

On-siteJohor Bahru, Johor, Malaysia

Full TimeEnterpriseHEALTHCARE

Job Summary

Lead and supervise day-to-day manufacturing, assembly, and packing operations to ensure production targets, quality standards, and delivery commitments are achieved. Coordinate workforce planning, production scheduling, and resource allocation while monitoring performance metrics to address bottlenecks and inefficiencies. Provide direct supervision, coaching, and performance management to Manufacturing Technicians and Operators, assigning work and ensuring tasks are completed safely and to quality standards. Oversee equipment setup, troubleshooting, and maintenance activities, collaborating with Engineering teams to resolve issues and improve reliability. Ensure compliance with ResMed Quality Management System, GMP, and OH&S standards by overseeing inspections, in-process controls, and CAPA investigations. Analyze operational data to drive Lean Manufacturing and continuous improvement initiatives that enhance efficiency and productivity.

Required Qualifications

  • Bachelor's Degree in Engineering, Manufacturing, Industrial Technology, or a related discipline
  • Minimum 5 years of manufacturing, production, or assembly experience in a regulated manufacturing environment
  • Minimum 2 years of supervisory, team leader, or people management experience
  • Strong knowledge of manufacturing processes, production operations, equipment maintenance, and quality systems
  • Demonstrated experience leading teams and managing production priorities in a fast-paced environment
  • Working knowledge of GMP, Quality Management Systems, and Occupational Health & Safety requirements
  • Strong problem-solving, analytical, decision-making, and organizational skills
  • Effective communication and stakeholder management skills across all organizational levels
  • Proficiency in manufacturing systems, production reporting tools, and Microsoft Office applications

Desired Qualifications

  • Experience within the medical device, healthcare, pharmaceutical, or other highly regulated manufacturing industries
  • Lean Manufacturing, Six Sigma, or Continuous Improvement certification
  • Experience with automated manufacturing equipment, calibration systems, and process validation activities
  • Knowledge of ISO 13485, FDA, or other relevant regulatory standards
  • Proven track record in driving operational improvements and leading change initiatives

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