QA Supervisor – Validation Team (5) - Khu Công Nghệ Cao, Thủ Đức

• Manage Process Validation and Cleaning Validation activities
• Oversee Equipment Qualification activities including DQ, IQ, OQ, and PQ
• Manage Utility System Qualification (HVAC, water system, compressed air, etc.)
• Conduct and supervise mapping tests and related qualification activities

GMP & Quality System

• Manage deviation handling and change control processes
• Review, revise, and maintain Validation SOPs and related GMP documentation
• Ensure all validation activities comply with GMP regulations and internal quality standards
• Support audits, inspections, and regulatory compliance activities

Coordination & Team Supervision

• Coordinate with Production, Engineering, QC, and other related departments
• Support validation planning and project execution for manufacturing equipment and utilities
• Supervise daily activities of validation team members
• Provide technical guidance and ensure timely completion of assigned tasks

• Minimum 5 years of experience in pharmaceutical company
• Experience in Validation & Qualification activities
• Experience working under GMP systems
• Intermediate or higher English communication skills
• Able to work overtime and weekends when required
• Diligent, responsible, and detail-oriented personality

Preferred Qualifications

• Strong understanding of Validation & Qualification systems
• Experience with pharmaceutical manufacturing equipment such as: Filling Machine; Isolator; Autoclave; Part Washer
• Other pharmaceutical production equipment
• Experience handling deviation and change control systems
• Experience reviewing and developing validation SOPs