Senior Scientist (ImmunoDx), DxD Hub

Agency for Science, Technology and Research (A*STAR); Singapore; On-site; SGD 80,000 - 120,000; Full time

Job summary

A leading research agency in Singapore seeks a highly motivated senior scientist for its ImmunoDiagnostic team. The role emphasizes developing regulated diagnostic products, particularly in protein assays. Responsibilities include leading project teams, mentoring staff, and managing lab operations. The ideal candidate will have 6-8 years in protein-based assay development with strong project management skills. This position offers the opportunity to drive impactful solutions while working closely with clinical and commercial stakeholders.

Qualifications

• 6-8 years of hands-on experience in protein-based assay development or IVD product development.
• Strong laboratory skills in pre-analytical and analytical techniques.
• Familiarity with regulatory and quality standards like ISO13485.

Responsibilities

• Lead cross-functional project teams through product development phases.
• Mentor junior scientists and ensure compliance with regulatory guidelines.
• Manage lab operations including housekeeping and consumables purchasing.

Skills

Protein-based assay development

Project management

Cross-functional team leadership

Critical thinking

Experimental design

Education

Education in Biochemistry, Cell Biology, Molecular Biology or Biotechnology

Job description

Seeking a highly motivated senior scientist to join the ImmunoDiagnostic team, focused on developing regulated diagnostic products and services, especially in protein-based assays.

The candidate will have a wide range of exposure of different technology platform, such as but not limited to ELISA, lateral flow, flow cytometry, electrochemical sensor, and mass spectrometry. This role combines deep scientific expertise with strong project management skills.

The successful candidate can be a project tech lead in the development for wide range of clinical application. Candidate will work closely with clinical and commercial stakeholders to deliver successful and impactful solutions.

Key Responsibilities

• Lead cross-functional project teams through different phases of product development, from feasibility to design transfer and verification/validation.
• Responsible for good records and standard operating procedures (SOPs) in accordance with confidential information requirement, quality system and regulatory guidelines.
• Responsible for mentoring junior scientists and refreshing the latest tech development and product landscape.
• Responsible for prompt supports and communications for internal and external stakeholders.
• Responsible for assay planning, and execution, analysing experimental data, troubleshoot technical challenges.
• Responsible for presentation for progress, finding, and solution to internal and external stakeholder
• Responsible for technical development timeline, budgets and resources.
• Contribute to project scoping and preparing project proposals with in-depth understanding in clinical workflow, clinical unmet needs, technology value proposition, economic value capture, clinical deployment, and product commercialization pathway.
• Contribute to product landscape study on safety dossier and technical note approved by regulators.
• Contribute to clinical study design, clinical trial in regulated diagnostic product settings.
• Manage and perform lab operations activities, including general laboratory and equipment housekeeping and qualifications, and consumables purchasing.

Requirements

• Education in Biochemistry, Cell Biology, Molecular Biology, Biotechnology, or a related field.
• At least 6-8 years of hands‑on experience in protein-based assay development or IVD product development, preferably in industrial, diagnostics or clinical laboratory setting, with at least 2-3 years in a project or team leadership capacity.

• Strong scientific foundation, demonstrated critical thinking abilities, and proven experience applying first-principles methodology.
• Strong track record in experimental design, troubleshooting, and optimisation of laboratory workflows.
• Laboratory skills in techniques in pre‑analytical and analytical, including extensive knowledge and hands‑on experience in protein‑based techniques.
• Familiarity with regulatory and quality standards for diagnostic assay development e.g. ISO13485.
• Demonstrated ability to manage complex projects and coordinate cross‑disciplinary teams.
• Training or certification in project management (e.g. PMP) is advantageous.
• Highly multi‑tasking with prompt response.

• Ability to articulate complex matter, which is guided by a great feedback loop.
• Great presentation skills for a mixed audience.
• Strong in identifying critical pathways and demonstrate problem‑solving abilities.
• Solid academic knowledge and a critical and innovative mindset.
• Extensive industrial relation and understanding of product landscapes.
• Optimistic and enthusiastic about continuous learning and professional development in the rapidly evolving field.
• A strong team player with a proactive and upbeat attitude.