
Visionary Engineer for Advanced Medical Diagnostics
3 days ago
Adiuvo Diagnostics is a techno-social enterprise focused on developing state-of-the-art platform technologies in optoelectronics. Our mission is to aid early disease detection and enable advanced healthcare diagnostics in low-resource settings.
This role requires a unique blend of hands-on technical expertise, cross-disciplinary knowledge, and leadership skills. The ideal candidate will design and execute cutting-edge R&D projects, build and mentor a strong engineering team, and deliver seamless innovation from concept to commercialization.
Key Responsibilities:
- Lead end-to-end R&D activities in hardware, optical systems, and device integration.
- Design, prototype, and validate novel hardware and optics solutions for imaging and diagnostic platforms.
- Translate product requirements into scalable technical designs in close collaboration with software, clinical, and regulatory teams.
- Build, guide, and mentor a multi-disciplinary team, fostering a culture of innovation and accountability.
- Oversee data-driven design decisions, ensuring precision, robustness, and compliance with regulatory standards.
- Drive experimental design, testing, and validation, including wet-lab support and cross-functional collaborations.
- Develop and maintain documentation required for regulatory submissions (FDA, CE, CDSCO).
- Manage project timelines, resource planning, and vendor coordination while staying hands-on with technical problem solving.
- Represent R&D leadership in discussions with external partners, investors, and collaborators.
Key Qualifications:
- Master's or PhD in Electronics, Optics, Physics, Biomedical Engineering, or related field.
- Strong technical expertise in hardware systems, optical instrumentation, sensors, and imaging technologies.
- Proven experience in leading experimental design, prototyping, and lab-based validation.
- Ability to manage and mentor engineers/scientists, while remaining hands-on in solving complex technical problems.
- Familiarity with regulatory documentation (e.g., ISO 13485, IEC 60601, FDA/CE submissions).
- Strong analytical mindset with ability to assimilate and interpret data.
- Excellent communication skills, with ability to collaborate across clinical, regulatory, and commercial teams.
- Prior experience in medical devices, diagnostics, or imaging platforms is highly desirable.
Why Join Us?
This is not a
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