Local Quality Manager – Manufacturing (Philippines)

About the role

You will support operational quality activities at our Philippines manufacturing site, working closely with the Local Operating Country Quality Manager and cross‑functional teams to keep the Quality Management System (QMS) effective and inspection ready. The role focuses on day‑to‑day quality operations, investigations, and continuous improvement to protect patient safety.

Key responsibilities

• Maintain and operate the local QMS in line with GSK standards, GMP and local regulations.
• Review production and batch documentation to support timely lot release decisions.
• Lead investigations, root‑cause analysis and corrective actions for deviations, complaints and audit findings.
• Conduct self‑inspections and support external audits and regulatory inspections.
• Monitor quality performance metrics, perform trending and drive continuous‑improvement actions.
• Coordinate quality activities with third‑party providers, suppliers and cross‑functional teams.
• Coach production and warehouse teams on good documentation practices and GMP behaviours.
• Manage quality records, retained samples and ensure data‑integrity compliance.
• Support risk assessments, change control and CAPA processes.

Required profile

• Experience in pharmaceutical or biopharmaceutical quality management.
• Strong understanding of Good Manufacturing Practices (GMP) and regulatory requirements.
• Proven ability to conduct investigations, root‑cause analysis and implement corrective actions.
• Familiarity with audit preparation and support for internal and external inspections.
• Excellent documentation and record‑keeping skills.

Required skills