Scientist Molecular

Borr Drilling; Singapore; On-site; SGD 70,000 - 90,000; Full time

Job summary

A leading diagnostics company in Singapore is seeking a motivated Scientist to lead the design and development of qPCR-based viral load quantification assays. The ideal candidate will have at least 3 years of experience in molecular diagnostics, a strong grasp of IVD product development, and the ability to ensure compliance with regulatory standards. This role offers the chance to innovate in a dynamic environment with cross-functional collaboration.

Qualifications

• Minimum of 3 years of hands-on experience in molecular assay development.
• Demonstrated work experience in an ISO 13485-compliant environment.
• Solid understanding of IVD product development processes.

Responsibilities

• Design, develop, and optimize qPCR-based IVD assays.
• Conduct design verification and validation studies.
• Collaborate with Regulatory Affairs and QA teams.

Skills

Molecular diagnostics

IVD product development

Data analysis

Technical training

Troubleshooting

Education

MSc or PhD in Biochemistry, Molecular Biology, 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.

Key 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

Basic Requirements of the Job

Education& Qualifications

MSc or PhD in Biochemistry, Molecular Biology, Molecular Genetics, or a related field

Experiences

• Minimum of 3 years of hands-on experiencein molecular assay development (e.g., qPCR)
• Demonstrated work experience in an ISO 13485-compliant environment
• Solid understanding of IVD product development processesand 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

Language skills

Native or Fluent in English and Mandarin is required; Fluent in Malay or Bahasa will be a plus.