Quality Assurance & Compliance Lead (QMS, ISO/AS)

globaltronic precision pte. ltd.; Singapore; On-site; SGD 60,000 - 90,000; Full time

Job summary

GlobalTronic Precision Pte. Ltd. in Singapore is seeking a QA/QMS specialist responsible for maintaining the quality management system, ensuring ISO 9001, AS9100 and medical requirements, and guiding audits and CAPA processes.

You will collaborate with Production, Engineering and QC to drive continuous improvement, manage documentation, control records, and support customer and supplier quality requirements.

Qualifications

• Diploma/Degree in Quality, Engineering, Manufacturing or related field.
• Minimum 5 years of QA/QMS experience in manufacturing or precision engineering.
• Good knowledge of ISO 9001.
• Knowledge of AS9100 and ISO 13485 is an advantage.
• Experience in medical, semiconductor or aerospace industries preferred.
• Experience in audits, CAPA, RCA and 8D.
• Good leadership, communication and problem-solving skills.

Responsibilities

• Manage and maintain the company's QMS, procedures and quality documentation.
• Ensure compliance with ISO 9001, AS9100, ISO13485 and customer requirements.
• Coordinate internal, customer and certification audits.
• Manage CAPA, RCA, 8D and corrective actions.
• Monitor quality performance and drive continuous improvement.
• Ensure proper document control, records and traceability.
• Work closely with Production, Engineering and QC to resolve quality issues.
• Work closely with the QC Manager to improve overall Quality Department efficiency and effectiveness.
• Support customer and supplier quality requirements.
• Drive improvements to reduce rejection, rework, scrap and customer complaints.

Skills

Quality Assurance

QMS

Audits

CAPA

RCA

8D

ISO 9001

AS9100

ISO13485

Leadership

Communication

Problem Solving

Education

Diploma/Degree in Quality, Engineering, Manufacturing

Job description

GlobalTronic Precision Pte. Ltd. in Singapore is seeking a QA/QMS specialist responsible for maintaining the quality management system, ensuring ISO 9001, AS9100 and medical requirements, and guiding audits and CAPA processes.

You will collaborate with Production, Engineering and QC to drive continuous improvement, manage documentation, control records, and support customer and supplier quality requirements.