QC Supervisor

Our mission is to enable early disease detection and provide insights for better patient care by harnessing the power of microRNA to augment traditional testing. Our vision is to be the world’s leading developer and provider of accurate, actionable, and affordable microRNA-powered diagnostic tests.

Job Location: Tukang

Job Summary

The individual will also participate in the investigation of nonconforming products and follow-up with the actions that arises from these inspections.

• Supervise QC Technicians to ensure smooth execution of routine QC operations.
• Plan and schedule daily QC routine and ad hoc testing.
• Oversee QC lab housekeeping, including cleanliness, equipment maintenance, document archival, and reagent inventory tracking.
• Perform routine QC testing of raw materials, in-process materials and finished goods.
• Evaluate data, draft and/or review QC reports, highlighting deviations from standard operating procedures.
• Consolidate and monitor QC data trends.
• Troubleshoot QC failures and raise nonconformance reports when needed. Investigate nonconformances to determine root causes.
• Draft and update QC work instructions.
• Support validation and stability studies for lab develpment and diagnostic products as needed.
• Contribute to the continuous improvement of laboratory procedures and processes to ensure compliance to GMPs.
• Apply good documentation practices on all records for better traceability, transparency, and the purpose of auditing.
• Perform any other duties as assigned.

• Diploma/Bachelor/ Master of Science/ Engineering or equivalent in Biotechnology, Biochemical, Biochemistry, Analytical Chemistry, Molecular Biology/ Life Science related courses.
• Appropriate experience may substitute for education.
• Have qPCR knowledge and experience in using qPCR machine.
• Familiar with the basic laboratory procedures. Relevant experience with laboratory testing, and QC of assays-based workflow will be an advantage.
• Able to work independently with minimal supervision and with others within and outside their function.
• Excellent organizational and time management skills.
• High degree of initiative and ownership.
• Possess a positive and willing-to-learn attitude.
• Good logical thinking and reasoning ability.
• Good Documentation Practices and ability to write protocols and procedures.
• People management experience including training, development and mentoring/coaching of technical staff would be an added advantage.
• 2-3 years of relevant experience in quality control and preferably in medical device manufacturing industry.
• GMP and/or ISO 13485 experience would be an added advantage.

We appreciate your interest in the above-mentioned position, however, due to overwhelming response, only shortlisted candidates will be contacted.

This role will be based at 2 Tukang Innovation Grove, #09-02 JTC MedTech Hub Singapore 618305.