Job Duties:

•     Participate in manufacturing & quality control of In-vitro diagnosis reagents;
•     Perform materials sourcing and quality control of incoming materials;
•     Conduct products stability study of new products;
•     Assist in production validation of new products;
•     To assist in developing, implementing and maintaining the documentation system, including the Standard Operating Procedures (SOPs) and other production documents;
•     Monitor and control production inventory using ERP system;
•     Conduct equipment monitoring and maintenance;
•     Handle general production and documentation work assigned by superiors;
•     Keep production areas and work environment clean and tidy by 5S.

 Requirements:

• Tertiary education level in life science or related discipline;
• Experience (1 year) with relevant background in science field; fresh graduate will also be considered;
• Experienced in DNA extraction, PCR is preferred;
• Experienced in handling equipment maintenance and calibration work is a plus ;
• Relevant experience or knowledge of ISO or GMP is preferred;
• Good communication skills;
• Team player attitude and proactive.

If you are passionate, driven and looking for a new and exciting opportunity within a successful and growing company, this may be the right role for you.

Please click “Apply Now” to submit your application.

For more info, please visit our web page at http://www.diagcor.com/en/

We will only consider applicants who apply directly to our firm and not through recruitment agencies. All applications will be treated in strict confidence. Personal data collected will be used for recruitment purposes only. Applicants who do not hear from us within 4 weeks may consider their applications unsuccessful and the applications will be destroyed within 6 months.