Scientist Molecular

Virtue Diagnostics; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A leading diagnostic solutions company in Singapore is seeking a highly motivated Scientist to lead the development of qPCR-based viral load quantification assays. The ideal candidate will have a strong background in molecular diagnostics and experience in a regulated environment, particularly in IVD product development. Responsibilities include design optimization and regulatory compliance, requiring excellent communication skills and willingness to travel. Fluency in English and Mandarin is essential.

Qualifications

• Minimum 3 years of hands-on experience in molecular assay development.
• Solid understanding of IVD product development processes.
• Excellent oral and written communication skills.

Responsibilities

• Design and optimize qPCR-based IVD assays.
• Conduct design verification and validation studies.
• Lead technical transfer of assays to production.

Skills

Molecular assay development

Technical transfer

Regulatory compliance

Data analysis and troubleshooting

Bioinformatic analysis

Effective communication

Education

MSc or PhD in Biochemistry or related field

Job description

We are seeking a highly motivated Scientist with strong expertise in molecular diagnostics and in vitro diagnostic (IVD) product development. This role offers the opportunity to lead the design, development, and validation of qPCR-based viral load quantification assays within a regulated environment.

The ideal candidate is an innovative thinker with experience across the entire IVD product lifecycle, including assay design, design verification/validation, technical transfer, and training. This position plays a key role in expanding and optimizing our diagnostic product portfolio and supporting global deployment.

Responsibilities

• Design, develop, and optimize qPCR-based IVD assays for viral load quantification
• Conduct design verification and validation studies to ensure performance, accuracy, and robustness
• Perform data analysis, troubleshooting, and optimization to ensure consistent assay reliability
• Ensure all products meet regulatory requirements(e.g., ISO 13485) and adhere to CLSI guidelines
• Lead the technical transfer of assays to overseas production or external partners
• Collaborate with Regulatory Affairs, QA, and Manufacturing teams to support product development and launch
• Maintain clear, complete, and compliant technical documentation and validation reports
• Support innovation by collaborating with cross-functional R&D teams to improve assay platforms and technologies
• Develop and deliver technical training to internal staff, customers, and end-users as needed

Requirements

• MSc or PhD in Biochemistry, Molecular Biology, Molecular Genetics, or a related field
• Minimum of 3 years of hands-on experience in molecular assay development (e.g., qPCR,)
• Demonstrated work experience in an ISO 13485-compliant environment
• Solid understanding of IVD product development processes and regulatory expectations
• Proven ability to troubleshoot and optimize molecular assays
• Excellent oral and written communication skills
• Skilled in bioinformatic analysis of genomes is an advantage
• Experience in regional technical support or customer training is a plus
• Willingness to travel when required
• Native or Fluent in English and Mandarin is required; Fluent in Malay or Bahasa will be a plus

Professional Competencies/skills

• Diligent with attention to detail
• Good characteristics in teamwork
• Dynamic and vigorous
• Self-motivated & self-sufficient
• Team player with the ability to work independently