Company transport pick up from Pasir Ris MRT, Yishun MRT, Khatib MRT, Woodlands MRT, Sengkang MRT, Hougang Ave 2
Excellent training and career development opportunities
Our client is one of the largest healthcare services groups in Asia. They provide world-class distribution, digital and commercial services to support the growing healthcare needs in this region.
Responsibilities:
Perform 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 facilities 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 requirement
Support to improve quality system and process of data collection
Work closely with inter-departments personnel to ensure quality is maintained throughout the organization
Support in audit operation and handling
Requirements:
Diploma in any related discipline
Minimum 2 years of experience in quality control works and preferable in assembly/ production environment
Experience in pharmaceutical/ medical device industry will be preferred
Knowledge in GMP, GSDP, and ISO is preferred
Possess strong work ethics, good interpersonal and communication skills
Meticulous, detailed, and thorough in work
Ability to work independently, self-motivated, and task-oriented
HOW TO APPLY:
Interested applicants, please click on "Apply Now" or email to REF31@stafflink.com.sg to submit your resume.
We regret only shortlisted candidates will be notified.