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Material Handler

QUASAR MEDICAL (SINGAPORE) PTE. LTD.

Singapore

On-site

SGD 30,000 - 45,000

Full time

30+ days ago

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Job summary

A leading medical manufacturing company in Singapore is seeking a Kitting Specialist responsible for ensuring materials for production are correctly kitted and comply with all safety and regulatory standards. The ideal candidate will maintain accurate records, oversee material transactions, and ensure timely job releases to production. An understanding of ISO 13485, GMP, and FDA regulations is essential for this position.

Qualifications

  • Knowledge of ISO 13485, GMP and FDA regulations.
  • Ability to perform accurate material transactions.
  • Experience maintaining compliance with safety features.

Responsibilities

  • Ensure materials for production are correct and timely.
  • Maintain proper stock recording and labelling.
  • Report safety issues immediately to the supervisor.
Job description
ESSENTIAL DUTIES AND RESPONSIBILITIES

Include the following. Other duties may be assigned.

  • Ensure kitted jobs release to production are correct such as part numbers and material requirement as stated in the job router.
  • Follow and observe proper FIFO (First In First Out) of materials.
  • Maintain proper material labelling and stocks recording.
  • Ensure actual quantity and ERP system are tally and accurate.
  • Ensure kitted jobs and released to production on time.
  • Perform material transactions on timely manner.
  • Use any safety features (machine guarding, interlocks, etc.) in place at respective machine in use and under any circumstances should not bypass.
  • Report immediately to direct supervisor if any safety features (machine guarding, interlocks, etc.) are not functional or present some alteration.
  • Perform cut to length process in accordance with the Manufacturing Process Instruction (MPI) and SA0379 document.
  • Keep records for the kitted jobs for future reference and easy traceability.
  • Perform line clearance and ensure cleanliness of kitting room.
  • Maintain and comply with ISO 13485, GMP and FDA regulations.
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