Medical Device Quality Inspector – ISO13485/GMP

QUASAR MEDICAL (SINGAPORE) PTE. LTD.; Singapore; On-site; SGD 30,000 - 45,000; Full time

Job summary

A medical device company in Singapore is seeking a QC Inspector responsible for supporting quality activities within operations. The role involves implementing standards for material inspection, assisting in quality issue investigation, and maintaining compliance with ISO13485 and FDA regulations. Ideal candidates should possess GCE 'O' level qualifications, 1-2 years of quality experience in medical device manufacturing, and strong communication skills. The position requires work in a multi-cultural team and cleanroom environment.

Qualifications

• 1-2 years of quality responsibility in Medical Device or Pharmaceutical Manufacturing.
• Knowledge of regulatory requirements and quality standards including FDA and ISO 13485.
• Ability to read/write manufacturing procedures and GMP requirements.

Responsibilities

• Support implementation of standards for incoming inspection and final product release.
• Perform incoming inspection for raw materials and finished products.
• Assist in the investigation and analysis of quality issues.

Skills

Excellent Communication Skills

Knowledge in ISO 13485

Computer Literacy (MS Office)

Ability to work in a multi-cultural team

Education

GCE 'O' level or equivalent

Diploma preferred

Job description

A medical device company in Singapore is seeking a QC Inspector responsible for supporting quality activities within operations. The role involves implementing standards for material inspection, assisting in quality issue investigation, and maintaining compliance with ISO13485 and FDA regulations. Ideal candidates should possess GCE 'O' level qualifications, 1-2 years of quality experience in medical device manufacturing, and strong communication skills. The position requires work in a multi-cultural team and cleanroom environment.