Scientist, Clinical Diagnostics Laboratory

Mirxes; Singapore; On-site; SGD 70,000 - 110,000; Full time

Benefits offered by this job

Restaurant nearby

Job summary

MiRXES is seeking a Scientist in the Clinical Laboratory to perform, validate, and interpret high-complexity molecular diagnostic testing using qPCR and NGS, in a CAP/CLIA-compliant environment. The role emphasizes developing assays, validating workflows, and generating timely patient results.

The successful candidate will design workflows, write SOPs, establish QC criteria, train staff, and collaborate with product teams to translate cutting-edge research into clinical services in Singapore.

Qualifications

• Advanced degree in molecular biology (MSc or PhD).
• Experience with qPCR and NGS in a clinical lab.
• Ability to design and validate molecular assays and SOPs.

Responsibilities

• Lead molecular assay development and validation in a clinical service lab.
• Implement validated LDTs or IVDs with hands-on leadership.
• Plan validation tests, establish QC, write reports.
• Train and mentor technical staff.

Skills

qPCR

NGS

Molecular biology

Leadership

Communication

Education

MSc/PhD MolBio

Job description

MiRXES is a Singapore-headquartered molecular diagnostic company with R&D, manufacturing, and clinical lab operations in Singapore, USA, Japan, and China. We specialize in microRNA technologies and the development, manufacturing, and provision of diagnostic test kits and clinical services.

Job Summary

The Clinical Laboratory is seeking a Scientist to perform, validate, and interpret high-complexity molecular diagnostic testing using quantitative PCR (qPCR) and Next-Generation Sequencing (NGS) technologies. The role is responsible for ensuring that all laboratory activities are conducted in compliance with CAP, CLIA, and applicable local regulatory requirements, while delivering accurate, reliable, and timely patient results.

The Scientist will play a key role in the development, validation, and clinical implementation of new assays and testing workflows. Responsibilities include designing and optimizing laboratory workflows, preparing standard operating procedures (SOPs), establishing quality control and acceptance criteria, developing validation protocols, executing validation studies, analyzing validation data, and preparing validation reports. The role also involves training and mentoring technical personnel to support the successful adoption of new testing methodologies within a regulated clinical laboratory environment.

Role & Responsibilities

• Lead the molecular assay development and validation efforts in a clinical service lab setting.
• Demonstrate hand-on leadership to successfully implement validated LDTs or IVDs in the laboratory.
• Design, plan and execute validation tests, establish QC criteria, write validation plan and report.
• Lead the SOP writing and technology transfer to the clinical operations team
• Propose and implement process improvements and EQA
• Work closely with other Scientists and Product Managers to provide scientific inputs related to company products and testing services.
• Support other commercial activities as required.

Desired Skills & Competencies

• Candidate is expected to have advanced research degree (MSc or PhD) in molecular biology or related field. Experiences in oncology or infectious disease are preferred.
• Strong understanding and working experiences on qPCR and NGS technologies is highly desirable.
• Experience in developing and implementing new molecular assays in a clinical laboratory is an added advantage.
• Be a ‘hands-on’ person who welcomes challenges, works independently or as part of a team, and can communicate effectively at all levels

This position is based in Singapore.

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