Validation Manager – Pharmaceutical Validation

About the role

Abbott, a global leader in healthcare, is seeking a Validation Manager to lead validation and qualification activities for its pharmaceutical manufacturing site in Vietnam. The role ensures that all processes, equipment, and systems meet stringent regulatory standards and support the delivery of high‑quality products.

Key responsibilities

• Plan, execute, and document validation and qualification of factories, equipment, machinery, APIs, excipients, manufacturing and cleaning procedures, and computerized systems.
• Maintain compliance with WHO‑GMP, PIC/S‑GMP, EU‑GMP, and other relevant regulatory frameworks.
• Develop and manage the Quality Management System (QMS) documentation related to validation activities.
• Collaborate with cross‑functional teams to ensure seamless integration of validation outcomes into production processes.
• Provide technical guidance and training on validation concepts and regulatory requirements.

Required profile

• University degree in Chemistry or Pharmacy.
• Minimum 5 years of experience in validation/qualification within the pharmaceutical or medical device industry.
• In‑depth knowledge of validation, qualification, and systematic GMP processes.
• Proven ability to master validation concepts, requirements, and execution.

Required skills

• Validation
• Qualification
• WHO‑GMP
• PIC/S‑GMP
• EU‑GMP
• Quality Management System (QMS)
• Pharmaceutical manufacturing processes
• API and excipient handling
• Cleaning procedures
• Computerized system validation

What we offer

• Opportunity to work with a global healthcare leader.
• Professional development in a highly regulated environment.
• Competitive compensation package.