QA Associate II

About the role

We are seeking an experienced Quality Assurance professional to support our pharmaceutical manufacturing operations in Taoyuan. The QA Associate II will maintain and improve quality systems covering raw material release, batch record review, stability, change control, audits, supplier management and more. This role contributes to delivering high‑quality drug products to global markets.

Key responsibilities

• Review incoming material documentation, perform sampling, ID testing and release activities.
• Inspect batch records and related documents to ensure completeness and accuracy for batch disposition.
• Manage stability program, stability chambers and annual inspection of reserve samples.
• Maintain change control, document control and training programs.
• Coordinate internal audits, regulatory inspections and supplier qualifications.

Required profile

• B.S. or higher in Science or Pharmaceutical Science with up to 3 years experience in biotechnology or GMP pharmaceuticals.
• Strong communication and interpersonal skills for cross‑functional collaboration.
• Excellent organizational and time‑management abilities.
• Fluent in English and Mandarin, both spoken and written.

Required skills

• Proficiency in Microsoft Excel.
• Proficiency in Microsoft PowerPoint.
• Proficiency in Microsoft Word.

What we offer

• Competitive salary with performance‑based incentives.
• Comprehensive health coverage (medical, dental, vision).
• Retirement savings plan with employer contributions.
• Paid time off and flexible work arrangements.
• Professional development and employee wellness programs.