Quality Assurance Specialist

About the role

The Quality Assurance Specialist will ensure that all secondary repackaging activities and related processes comply with Zuellig Pharma's Quality Management System (QMS). This role supports product quality, regulatory compliance, and customer satisfaction across the company's operations in Asia.

Key responsibilities

• Maintain compliance with the QMS for secondary repackaging activities.
• Assess returned deliveries that require QA review and document findings.
• Report product quality complaints and coordinate corrective actions.
• Verify on‑site records under QA oversight, including calibration records and inspection reports.
• Act as the primary QA contact for PDEA inspection activities.
• Align QA activities with business objectives, regulatory requirements, industry standards, and client expectations.
• Promote a culture of quality and compliance throughout the organization.

Required profile

• Bachelor's degree in pharmacy, life sciences, or a related field.
• Certification in Quality Management Systems (e.g., ISO 9001, ISO 13485) is preferred.
• Licensed pharmacist status is preferred.

Required skills

• ISO 9001
• ISO 13485

What we offer

• Inclusive environment that values diversity, equity, and inclusion.
• Opportunities to gain comprehensive knowledge of the dynamic healthcare industry across multiple Asian markets.
• Flexibility to balance work and personal life.
• Robust Total Rewards program supporting overall well‑being.
• Career growth and development opportunities within a multibillion‑dollar organization.