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

Interested applicants please send your resume to alexis.bo@experis.com.sh

Bo Zhuang Mian

R1872731

Manpower Staffing Services (S) Pte Ltd

02C3423

Alexis, Zhuang Mian Bo EA License No.: 02C3423 Personnel Registration No.: R1872731