Job:

• Performs QMS document control including processing, approval, distributing and archiving.
• Coordinate the revision, review and approval of procedures and other ISO, GMP documents
• Process audit in accordance to ISO, GMP and regulatory requirement.
• Facilitate Change control and support applicable validation requirement.
• To maintain CAPA system and facilitates its activities in order to ensure timeliness, effectiveness and compliance of the system.
• Support in managing and responding to complaint investigation.
• Ensure supplier's performance to quality and regulatory requirement through qualification, audit and CAPA program.
• Ensure compliance to ISO procedures, GMP and all regulatory requirements.
• Support to improve quality systems and process of data collection
• Work closely with inter-departments personnel to ensure quality is maintained throughout the organization.
• Support in audit preparation and handling

Requirements:

• Diploma in any related discipline
• 2 years' experience in quality control works and preferable in manufacturing/assembly/production environment
• Experience in pharmaceutical industry will be preferred
• Knowledge in GMP, GSDP and ISO preferred
• Possess strong work ethics, good interpersonal and communication skills

Song Zhao Hui EA License No. 02C3423 Personnel Registration No. R1761205

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