Company Overview: Our client is a global leader in life sciences and biopharmaceuticals, offering unparalleled opportunities to impact healthcare. The Regional Quality Director will play a crucial role in leading and inspiring quality teams, ensuring the highest standards of quality, and directly impacting the safety and efficacy of life-saving treatments for patients worldwide.
Roles and Responsibilities:
- Team Leadership: Build and motivate high-performing teams to meet business needs while maintaining quality and regulatory standards.
- Global Coordination: Collaborate with international teams and stakeholders to align quality strategies across regions.
- Resource and Financial Management: Efficiently manage resources and financial plans to achieve business and quality goals.
- Audit Preparedness: Ensure the region is always ready for client, internal, and regulatory audits.
- Issue Investigation: Conduct thorough investigations into incidents, complaints, and data audits to ensure resolution.
- Regulatory Compliance: Maintain strict adherence to regulatory standards in all operations and reporting.
- Risk Management: Identify and mitigate key risks through effective collaboration.
- Document Oversight: Review and approve essential GxP documents and quality records accurately.
- Performance Reporting: Provide senior management with insightful performance metrics.
Qualifications:
- Bachelor's degree in Life Sciences; MSc or PhD preferred.
- Over 10 years of management experience in quality teams.
- More than 10 years in a GMP environment within a regulated industry (preferably pharmaceutical or biopharmaceutical).
- Strong global mindset, ability to work across time zones, and skills in relationship-building, negotiation, and change management.
To apply, click on the apply button or reach out to Kee Siang.
EA License No: 16S8194/R24119765
Company Overview: Our client is a global leader in life sciences and biopharmaceuticals, offering unparalleled opportunities to impact healthcare. The Regional Quality Director will play a crucial role in leading and inspiring quality teams, ensuring the highest standards of quality, and directly impacting the safety and efficacy of life-saving treatments for patients worldwide.
Roles and Responsibilities:
- Team Leadership: Build and motivate high-performing teams to meet business needs while maintaining quality and regulatory standards.
- Global Coordination: Collaborate with international teams and stakeholders to align quality strategies across regions.
- Resource and Financial Management: Efficiently manage resources and financial plans to achieve business and quality goals.
- Audit Preparedness: Ensure the region is always ready for client, internal, and regulatory audits.
- Issue Investigation: Conduct thorough investigations into incidents, complaints, and data audits to ensure resolution.
- Regulatory Compliance: Maintain strict adherence to regulatory standards in all operations and reporting.
- Risk Management: Identify and mitigate key risks through effective collaboration.
- Document Oversight: Review and approve essential GxP documents and quality records accurately.
- Performance Reporting: Provide senior management with insightful performance metrics.
Qualifications:
- Bachelor's degree in Life Sciences; MSc or PhD preferred.
- Over 10 years of management experience in quality teams.
- More than 10 years in a GMP environment within a regulated industry (preferably pharmaceutical or biopharmaceutical).
- Strong global mindset, ability to work across time zones, and skills in relationship-building, negotiation, and change management.
To apply, click on the apply button or reach out to Kee Siang.
EA License No: 16S8194/R24119765