Zuellig Pharma is a leading healthcare solutions company in Asia, and our purpose is to make healthcare more accessible to the communities we serve. We provide world-class distribution, digital, and commercial services to support the growing healthcare needs in this region.

The company was started a hundred years ago and has grown to become a multibillion-dollar business covering 17 markets with over 12,000 employees. Our people serve more than 200,000 medical facilities and work with over 450 clients, including the top 20 pharmaceutical companies in the world.

Purpose of the Role: Responsible for maintaining the quality and compliance of secondary repackaging processes by performing daily quality checks, updating product specifications and records, supporting audits and investigations, and providing administrative support to the Quality Assurance team, ensuring the product meets all relevant regulations.

Expectations of the Role:

• Be a member in Quality Assurance team on daily quality control in process checking and take relevant quality control job duty at the production line
• Responsible for secondary repackaging materials release process
• Review and update the product specification, work instruction, batch production record or other relevant documents for the secondary repackaging production
• Participate in quality/regulatory inspections and quality-related visit
• Provide administrative support in client quality audits and customer product quality complaints Ensure quality documentation and records are maintained according to the internal procedures and the quality management system
• Provide ad hoc administrative support to the Quality Assurance team as assigned

Attributes Required:

Must-Have:

• High Diploma or above with over 2 years of related experience in quality control or equivalent experience
• Proficiency in Microsoft Office (Word, Excel)
• Good command of both written and spoken English and Chinese (including Cantonese)

Advantage to Have:

• With work experience in FMCG or Pharmaceutical is preferable
• Familiar with local applicable regulations ISO 9001/GMP/GSDP is an advantage
• Good team player with strong sense of responsibility, self-motivated and independent

Why Join Zuellig Pharma:

• We are committed to fostering an inclusive environment where our employees can learn, grow, and achieve shared success.
• We champion diversity, equity, and inclusion, ensuring every individual feels valued, respected, and treated fairly.
• As a leading multi-market healthcare solutions provider, we empower our employees to gain comprehensive knowledge and expertise in the dynamic healthcare industry across the region.
• Enjoy the flexibility to effectively balance your work and personal life while taking charge of your career journey through our empowering growth opportunities.
• Our Total Rewards program is designed to support your overall well-being in every aspect.

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