Type: Full-Time
Location: Baltimore, MD (On-Site)
Role Summary:
We are seeking a Senior Scientist with a strong background in molecular diagnostics and instrumentation to help lead the development of our PCR-based assays and guide the advancement of our integrated testing platform. This role is ideal for a motivated scientist with a startup mindset, technical breadth, and leadership skills to mentor and grow a team.
How to apply:
Please submit your application through our LinkedIn job posting found at this link.
Key Responsibilities:
- Lead the design, development, and validation of PCR/qPCR assays for infectious disease detection.
- Drive experimental planning and execution across molecular biology and engineering domains.
- Guide junior scientists, engineers, and technicians in laboratory work, data analysis, and project execution.
- Collaborate closely with hardware, software, and assay teams to integrate sample-to-answer workflows.
- Support prototyping and rapid iteration of fluidic and thermal systems, including 3D printing and light machining.
- Oversee quality documentation and design control activities in compliance with ISO 13485/FDA expectations.
Qualifications (Required)
- PhD. in Molecular Biology, Biomedical Engineering, Mechanical Engineering, or related area with a minimum of 3 years related industry experience, or B.S/M.S.
- Experience in qPCR primer and probe design and optimization
- Ability to work in a biosafety level 2 lab environment
- Experience with bacterial cell culture techniques
- Excellent communication skills (written, verbal) and an independent problem solver
- Experience with nucleic acid extraction and characterization techniques
Qualifications (Preferred)
- Experience with highly multiplexed nucleic acid probe-based assays
- Experience with lyophilization and development of shelf-stable reagents
- Rapid prototyping capabilities (e.g. Computer-aided design, 3D-printing, laser-cutting)
- Familiarity with design and operation of integrated diagnostic instrumentation (fluidics, thermal control, optics, etc.).
- Experience working with ISO13485 quality management systems, design controls, verification and validation
- Experience with FDA 510(K) and CLIA-waiver regulatory trials and submission
- Proficiency in code-based data analysis techniques (R, python).
Benefits
- Flexible paid time off (PTO) and company holidays
- Full health benefits including medical, dental, and vision coverage
- 401(k) with employer matching