Ensure the pharmaceutical quality management system, GMP compliance and regulatory requirements are effectively established, implemented, monitored and continuously improved through core QA activities
Job Summary
Ensure the pharmaceutical quality management system, GMP compliance and regulatory requirements are effectively established, implemented, monitored and continuously improved through core QA activities.
Operate and maintain the Quality Management System (QMS), coordinate and track audits, manage exceptions, deviations and CAPA, and handle complaints, recalls and returned products.
Act as QA focal point coordinating quality activities at site, liaise with internal departments and corporate teams, and ensure QA activities are GMP-compliant, timely and properly documented.
Matching Summary
Ensure the pharmaceutical quality management system, GMP compliance and regulatory requirements are effectively established, implemented, monitored and continuously improved through core QA activities.
Skills & Requirements
Must-have
Quality Management System (QMS)
GMP compliance
SOP compliance
Manage exceptions, deviations and CAPA
Handle complaints, recalls and returned products
Nice-to-have
Continuous improvement actions
Cross-functional working skills
Growth mindset
Key Requirements
Minimum 3 years’ experience in pharmaceutical manufacturing
University Pharmacist or Bachelor in Chemistry, Biology or related disciplines
GMP-WHO training completed
Hands-on experience with GMP, CAPA and audits is an advantage