Quality Assurance (QA) Associate Director, GCP QMS / Life Sciences MNC

Integrity Partners Pte. Ltd.; Singapore; On-site; SGD 80,000 - 110,000; Full time

Job summary

A leading life sciences innovator is seeking a seasoned Quality Assurance expert for their Singapore office to spearhead global GxP compliance. The ideal candidate will lead regulatory audits, drive continuous improvement initiatives, and ensure inspection readiness. Applicants should have over 8 years of experience in GxP Quality Assurance within the pharmaceutical or biotech sector. This is a pivotal role for those passionate about compliance and strategic leadership.

Qualifications

• Minimum 8+ years of experience in GxP Quality Assurance or Clinical Quality Management.
• Comprehensive knowledge of global regulatory frameworks.
• Experience in managing complex inspections.

Responsibilities

• Perform expert reviews of GCP, GLP, and GVP SOPs.
• Coordinate and lead regulatory audit responses.
• Analyze quality trends to drive continuous improvement.
• Mentor teams on GxP best practices.
• Integrate new regulatory requirements into workflows.
• Evaluate quality metrics for trend identification.
• Deliver training programs for inspection readiness.

Skills

GCP

GLP

GVP

Risk management

Stakeholder influence

Education

Degree in Life Sciences, Pharmacy, or related field

Job description

Are you a seasoned candidate in Pharmacovigilance Quality Assurance (PVQA) with a passion for compliance, risk management, and strategic leadership?

Our client, a leading innovator in the life sciences sector, is seeking a seasoned Quality Assurance expert to spearhead their global GxP compliance framework. In this pivotal role, you will serve as the definitive Subject Matter Expert (SME) for GCP, GLP, and GVP standards, ensuring that the organization’s global operations are not only compliant but best-in-class.

Key Responsibilities:

• Perform expert reviews of GCP, GLP, and GVP related SOPs to identify gaps and ensure global consistency.
• Coordinate and lead the response for regulatory audits, providing strategic input for documentation and follow‑up actions.
• Analyze quality trends and metrics to drive continuous improvement initiatives across the QMS.
• Use audit data to sharpen the QMS and mentor teams on GxP best practices.
• Partner with cross‑functional teams to integrate new regulatory requirements into existing workflows.
• Evaluate quality metrics and audit findings to identify trends, driving a culture of continuous improvement within the QMS.
• Develop and deliver specialized training programs to enhance inspection readiness across various business units.

What We’re Looking For:

• A degree in Life Sciences, Pharmacy, or a related field is required.
• A minimum of 8+ years of experience within GxP Quality Assurance or Clinical Quality Management in the pharmaceutical or biotech sector.
• Comprehensive knowledge of global regulatory frameworks, including experience managing complex inspections.
• Proven ability to influence stakeholders within a global matrix environment.

How to Apply:

• Interested applicants may apply by sending in your updated résumé (in MS Word format) to my email or apply directly.
• Consultant: Tan Weixiang