RESPONSIBILITIES

• Prepare and review SOPs in order to comply with GMP and regulatory requirement
• Prepare production documents for production such as MBPR/MF
• Prepare equipment validation document such as IQ/OQ/PQ and responsible for the related activities
• Responsible for training for production staff and prepare the related document
• Handling Data Entry
• Assisting project management issue
• Other Ad Hoc issue

REQUIREMENTS

• Higher Diploma or above, preferably in Pharm Sci / Science disciplines
• Knowledge of GMP is an advantage
• MS office and Chinese word typing
• Willing to learn and responsible
• Good command of both written and spoken Chinese and English
• Fresh graduate will be considered

Interested parties please send CV and expected salary by clicking "Apply Now" for interview.

Data collected will be used for recruitment purpose only.