ABOUT THE COMPANY
VedaBio is revolutionizing molecular biology with its breakthrough platform for ultra-rapid molecular detection of multiplexed analytes, delivering best-in-class accuracy without the need for target amplification. Our CRISPR Cascade™ platform is poised to emerge as a new gold standard tool to empower decision-making across multiple industries.
Veda is derived from the Sanskrit word for creation of knowledge. With our team of leading experts, we operate at the forefront of scientific innovation to push the limited of what’s possible in the field of molecular detection. Backed by top tier venture capital investors, VedaBio’s first applications are in molecular diagnostics.
ABOUT THE OPPORTUNITY
VedaBio is looking for an exceptional candidate to be an integral part of our mission to disrupt molecular detection, joining a world-class team that is redefining and pushing the boundaries of what is possible with our novel biochemistries. As part of a highly collaborative and cross-functional team, you will bring your technical depth and breadth, curiosity, and creativity to be a key technical contributor in developing highly multiplexed molecular IVD CRISPR assays and integrating them into our products.
ESSENTIAL DUTIES AND RESPONSIBILITIES
- Work in a highly cross-functional team to drive technology forward through development and commercialization.
- Act as a project leader and subject matter expert in collaboration with internal teams and external partners to advance product development timelines.
- Apply in-depth molecular biology knowledgeand experience in the development of CRISPR-based molecular diagnostic assay systems, including development of enzyme reagents and assay workflows, consumables, and instrumentation.
- Hands-on work in the laboratory to execute experimental designs/studies may be required.
- May supervise junior scientists/research associates.
- Lead planning and execution of experiments to contribute to maturing our in-vitro diagnostic assays from early concept through feasibility, development, and verification/validation.
- Optimize and troubleshoot assay designs, workflows, and/or reagentsthrough a combination of technical experience, literature review, critical thinking, and creativity.
- Prepare reports and documentation in the process of developing regulatory submissions.
- Become familiarand stay up to date with the relevant scientific CRISPR literature and landscape technologies and contribute to our IP portfolio.
- Routinely summarize methods and results for internal and external audiences (internal technical meetings, external scientific conferences, regulatory submissions)
REQUIRED EXPERIENCE AND SKILLS
- PhD in life sciences (Biology, Chemistry, Biochemistry, Microbiology), engineering, or related field with 6+ years experience in an industry setting, or equivalent experience (Masters Degree with 9+ years or BS with 12+ years of relevant experience in an industry setting)
- Proven track record and experience developing molecular diagnostic products in an IVD or CLIA setting
- Leadership experience and effective people management experience required
- Excellent analytical, problem-solving, and communication skills, and strong data analysis skills.
- Self-motivated with a strong work ethic and a strong sense of accountability
- Excellent written and verbal communication skills; experience presenting data to internal teams.
- Strong data and statistical analysis skills. Experience with python or other programming languages is desirable.
- Ability to workindependently and collaboratively in a fast-paced and highly cross- functional R&D start-up environment.
- Highly organized, detail-oriented, self-motivated, and strong sense of accountability.
Work Environment
Employee frequently works in a professional office or lab environment with lots of computer equipment, tools, and moderate amounts of noise and activity. Employee may occasionally be required to travel. The work environment is fast-paced and demanding. Off-shift, weekend and overtime duties may be required as assigned by the manager.
VedaBio provides a competitive total compensation package including the ability to purchase company stock, receive annual bonuses and participate in benefit and 401k programs The anticipated salary range for candidates who will work in San Diego, CA is $145,000 to $175,000.
The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. VedaBio is a multi-state