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
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
Interested applicants please send your resume to email@example.com
Bo Zhuang Mian
Manpower Staffing Services (S) Pte Ltd
Alexis, Zhuang Mian Bo EA License No.: 02C3423 Personnel Registration No.: R1872731