Key Roles and Responsibilities:

• Assist in developing, implementing and maintaining the documentation system and quality management system;
• Perform routine inspection on products at various stages on the production line to implement the GMP policy;
• Assist in performing ad hoc project and other QA-related duties.

Requirements:

• Higher Diploma or Degree holder in Pharmaceutical Studies or other science related discipline;
• Hands-on GMP experience in pharmaceutical industry will be an definite advantage;
• Hardworking, initiative, self-motivated and fast learner;
• Strong communication skill, good command of English and Chinese;
• Good knowledge of MS Office and Chinese word processing;
• Fresh graduates are also considered.