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    Research and Development Manager - San Diego, United States - VedaBio

    VedaBio
    VedaBio San Diego, United States

    5 days ago

    Default job background
    Pharmaceutical / Bio-tech
    Description

    ABOUT THE COMPANY

    VedaBio is revolutionizing molecular biology with a breakthrough platform for rapid, multiplexed molecular diagnostic detection without the need for target amplification. Our CRISPR CascadeTM platform is poised to emerge as a new gold standard in molecular biology. By combining the power of our platform with a strong focus on delivering products to solve real clinical and industrial needs, we are preparing to transform clinical and operational workflows for the betterment of patients and consumers in every setting.

    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.
    • Lead multiple projects/work-streams, and serve as a subject matter expert in collaboration with internal teams and external partners to advance product development timelines.
    • Apply in-depth molecular biology knowledge and experience in the development of CRISPR-based molecular diagnostic assay systems, including development of enzyme reagents and assay workflows, consumables, and instrumentation.
    • Some hands-on work in the laboratory to execute experimental designs/studies may be required.
    • Supervise and develop junior scientists and research associates.
    • Plan 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 reagents through a combination of technical experience, literature review, critical thinking, and creativity.
    • Prepare reports and documentation in the process of developing regulatory submissions.
    • Become familiar and 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).
    • Experience with molecular diagnostics, IVD assay development, and with handling infectious agents strongly preferred.
    • Proven leadership and effective people management experience required.
    • Broadly experienced in hands-on molecular biology techniques including extraction, amplification, and detection technologies, and with handling and manipulation of nucleic acids. Previous experience with CRISPR systems is a plus.
    • Demonstrated experience with biochemical assay development and optimization.
    • Excellent analytical, problem-solving, and communication skills.
    • Strong data and statistical analysis skills.
    • Ability to work independently 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.

    OTHERS

    • Must be eligible to legally work in the USA.
    • This position is located in San Diego (Torrey Pines), California.

    While performing the duties the employee is:

    • Constantly required to sit, and to reach to use computers and other office or lab equipment.
    • Occasionally stand for extended periods of time, up to four (4) hours/time.
    • Occasionally required to lift up to 20 pounds.
    • Constantly required to view objects at close and distant ranges.
    • Frequently required to communicate with others.

    Note: For the purpose of this summary, occasionally is used to represent up to 1/3 of the time given to the work day, frequently represents 1/3 to 2/3 of the time and constantly represents 2/3 or more of the time.

    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 $150,000 to $190,000.

    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 employer, and this salary range may not reflect positions that work in other states.



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