Jobs

We are seeking a highly skilled and motivated Lateral Flow Assay (LFA) Development Scientist to lead the design, development, and validation of novel in-vitro diagnostic assays. The ideal candidate will have deep expertise in assay sensitivity, specificity, and reproducibility, with a strong background in assay optimization and scale-up. You will collaborate with cross-functional teams to ensure the seamless transition of assay designs from R&D to production, and contribute to advancing diagnostic solutions that improve patient outcomes.

Key Responsibilities:

• Lead the development and validation of novel lateral flow assays focusing on assay sensitivity, specificity, and reproducibility.

• Design, optimize, and scale up LFA systems, integrating critical assay components and control systems to ensure robust performance.

• Troubleshoot and refine assay development processes to meet regulatory standards and address key performance parameters.

• Collaborate with cross-functional teams (mechanical, software, sourcing) to facilitate smooth technology transfer from R&D to production.

• Identify and work with external vendors for material sourcing, assay customization, and large-scale manufacturing.

• Conduct comprehensive system and subsystem performance evaluations using clinical samples in both lab and field environments.

• Maintain meticulous records of experimental protocols, data analyses, and interpretations in line with best lab practices.

• Drive strategic collaborations for acquiring and validating clinical samples such as blood, urine, and serum.

Required Qualifications:

• Master’s or PhD in Biotechnology, Biochemistry, or related Life Sciences field.

• Minimum 5 years industry experience in lateral flow assay or in-vitro diagnostic product development.

• Expertise in lateral flow assay design, protein detection methods (ELISA, immunochemistry), and experience with biomarkers or bioassays.

• Strong laboratory skills including antibody conjugation, protein purification, and assay troubleshooting.

• Proven ability to identify and overcome technical challenges related to assay performance and scalability.

Preferred Skills:

• Demonstrated leadership in LFA development, with experience in clinical diagnostics and regulatory compliance.

• Proficiency in statistical analysis tools such as Excel, R, or equivalents for data interpretation.

• Strong project management skills and experience working collaboratively across multidisciplinary teams.

• Excellent written and verbal communication skills, with the ability to clearly document complex protocols and present results effectively.