Medical Device Process Specialist (GMP/ISO)

Quasar Medical; Singapore; Presencial; SGD 42.000 - 66.000; Jornada completa

Descripción de la vacante

Quasar Medical in Singapore is seeking a Process Technician to maintain, monitor and improve manufacturing processes within our medical device production environment. You will work closely with production, quality and engineering teams to ensure processes comply with regulatory standards and quality requirements.

Responsibilities include overseeing daily operations, training staff, supporting engineering studies, reviewing documentation, troubleshooting, and driving process improvements.

Formación

• GCE O level or higher with 1-3 years assembly or technician experience in medical devices.
• Familiarity with GMP/ISO documentation and cleanroom procedures.
• Proficient in Microsoft Office; AutoCAD a plus.

Responsabilidades

• Monitor and control manufacturing processes to ensure quality.
• Train production personnel per SOPs and GMP guidelines.
• Support engineering studies and process improvements.
• Maintain DHRs, SOPs, ECOs, and related documentation.
• Conduct regular inspections and tests to ensure regulatory compliance.
• Assist in NPI transitions and production support.
• Ensure safety and environmental compliance; rotate shifts.

Conocimientos

Manufacturing processes

GMP/ISO knowledge

Problem solving

Educación

GCE O level or higher

Herramientas

AutoCAD

Microsoft Office

Descripción del empleo

Quasar Medical in Singapore is seeking a Process Technician to maintain, monitor and improve manufacturing processes within our medical device production environment. You will work closely with production, quality and engineering teams to ensure processes comply with regulatory standards and quality requirements.

Responsibilities include overseeing daily operations, training staff, supporting engineering studies, reviewing documentation, troubleshooting, and driving process improvements.