Job ref no.: CT3117832-01#0049
Zuellig Pharma Ltd

Quality Assurance Officer

Zuellig Pharma Ltd

  • 5-day week
  • 13-month pay
  • Competitive pay
  • Discretionary bonus
  • Education subsidies
  • Insurance plan
  • Medical plan
  • … + 1 more

Job Responsibilities:

  • Maintaining QMS and comply to all the requirements like Change control, Deviation CAPAs, Training, Risk management documentation
  • Responding to Quality related market complaints & documentation.
  • Responsible for supporting deviation close out, writing investigation reports and initiating/following up on corrective and preventative actions
  • Leading Quality based projects working as part of a multidisciplinary team as required
  • Responsible for supporting quality related customer complaint investigations and trending activities
  • To promote continuous improvement of the Quality Management System
  • Providing support and advice during cross functional investigations / projects and as required
  • Able to provide direct support during customer and regulatory audits
  • Approving pre and post execution validation documents
  • Able to provide training in all aspects of Quality Management Systems and GMP including procedural updates
  • For Quality Assurance Assistant who is registered as Department of Health Quality Assurance Officer, additional empowerment in dedicated area as below:
  • Dispose of starting materials and packaging materials (e.g. release, rejection, destruction)
  • Approve and review of batch records and product specifications
  • Release the finished redressed product at dedicated site according to the product specifications, local regulatory requirements and Zuellig Pharma SOP requirements.
  • Effective management of deviation, product/materials nonconformity, recall, and product complaints related to secondary packaging (includes investigation and corrective actions)

Qualifications & Experience:

  • Degree in related disciplines
  • Qualification on packaging of pharmaceutical products, together with a certified GMP training
  • At least 3 years relevant quality management experience in pharmaceutical industry
  • Experience / exposure in dealing with Quality, Regulations & Enforcements within the local laws of for Pharmaceutical industry.
  • Exposure to training and related expertise is an advantage

We offer competitive remuneration package to the right candidate. Interested parties please apply with full resume stating present and expected salary to : The Human Resources Manager, Zuellig Pharma Ltd., Suite 608, 6/F, Devon House, Taikoo Place, Quarry Bay, Hong Kong or email to
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More job information
Job ref no. CT3117832-01#0049
  • N/A
Job Function
  • Tsing Yi
Employment Term
  • Full-time
  • 3 years - 8 years
Career Level
  • Non-management level
  • Degree