Quality Leader, Lab Operations & Compliance

GMP Technologies; Singapore; On-site; SGD 120,000 - 180,000; Full time

Job summary

GMP Technologies seeks a Senior Manager, Quality - Lab Environment to lead the Quality department within a newly established laboratory in Singapore. The role will oversee QA, QMS, vendor oversight, batch disposition, and regulatory compliance to ensure lab operations meet global standards.

Responsibilities include driving quality strategy, managing a growing team, and guiding technology transfer for clinical material production, while coordinating with regulators and inspectors to uphold GMP

Qualifications

• 10+ years in Quality Lead roles in pharma/biotech/healthcare
• Extensive knowledge of quality systems, validation, and vendor management
• Strong leadership and communication abilities to influence cross-functional teams

Responsibilities

• Establish and oversee QA functions and QMS for lab programs and services
• Implement and maintain QMS to ensure compliance with policies and regulations
• Drive quality metrics and continuous improvement through management reviews
• Provide quality oversight for technology transfer during clinical material production
• Serve as Quality representative to regulatory authorities and inspections
• Lead talent development and build a high-performance quality organization
• Alert senior management to significant quality and compliance risks
• Collaborate with cross-functional teams to ensure GxP-compliant programs

Skills

Leadership

Communication

Problem solving

Critical thinking

Education

Bachelor's or Master's in Science/Pharma

Job description

GMP Technologies seeks a Senior Manager, Quality - Lab Environment to lead the Quality department within a newly established laboratory in Singapore. The role will oversee QA, QMS, vendor oversight, batch disposition, and regulatory compliance to ensure lab operations meet global standards.

Responsibilities include driving quality strategy, managing a growing team, and guiding technology transfer for clinical material production, while coordinating with regulators and inspectors to uphold GMP