Quality System Officer
1 week ago
**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
- Minimum 2 years’ experience in quality control works and preferable in 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
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