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Overview
Be Part of a High-Performing Team
This innovative biopharmaceutical company is dedicated to advancing therapies for rare diseases, with a strong focus on next-generation gene therapy solutions. The R&D team in Lebanon, NH, operates in a collaborative, fast-paced environment where experimental and computational scientists work side by side to drive discovery and innovation. The lab fosters creativity, scientific rigor, and mentorship, providing an opportunity to contribute directly to groundbreaking advancements in biologics research.
What’s In Store For You
Hands-on role in a state-of-the-art research lab, supporting cutting-edge gene therapy programs
Opportunity to lead projects and mentor junior scientists
Exposure to novel discovery efforts with real-world impact on rare disease treatment
Long-term career trajectory, with conversion from contract to full-time employee after 6 months
How You Will Make an Impact
Lead research efforts focused on engineering and discovery of viral vectors for gene therapy
Design and optimize molecular and cellular assays for high-throughput screening
Conduct viral vector development, transfection, transduction, and sequencing-based analysis
Build and characterize viral vector libraries using advanced molecular biology methods
Perform mammalian cell culture, primary cell work, and provide in vivo study design support
Prepare and analyze Next- Sequencing (NGS) libraries, with exposure to long-read sequencing (PacBio)
Document protocols, deliver reports, and present results to cross-disciplinary teams
Mentor junior scientists and support lab operations while maintaining high-quality standards
Are You an Accomplished Scientist Ready to Drive Innovation in Gene Therapy?
PhD in cell biology, virology, immunology, molecular biology, bioengineering, or related field with 2+ years of industry experience (academic considered), OR Master’s with 8+ years hands-on experience
Proven expertise in viral vectors; direct AAV experience strongly
Strong foundation in molecular biology (cloning, PCR/qPCR/ddPCR, DNA/RNA workflows)
Skilled in mammalian and primary cell culture
Background in viral vector engineering, library preparation, and screening
NGS sample preparation experience required; PacBio or long-read sequencing strongly desired
In vivo study design experience is a plus
Prior leadership or mentorship experience , with potential to transition into a leadership role after conversion
Strong communication, problem-solving, and organizational skills
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This innovative biopharmaceutical company is dedicated to advancing therapies for rare diseases, with a strong focus on next-generation gene therapy solutions. The R&D team in Lebanon, NH, operates in a collaborative, fast-paced environment where experimental and computational scientists work side by side to drive discovery and innovation. The lab fosters creativity, scientific rigor, and mentorship, providing an opportunity to contribute directly to groundbreaking advancements in biologics research.
What’s In Store For You
Hands-on role in a state-of-the-art research lab, supporting cutting-edge gene therapy programs
Opportunity to lead projects and mentor junior scientists
Exposure to novel discovery efforts with real-world impact on rare disease treatment
Long-term career trajectory, with conversion from contract to full-time employee after 6 months
How You Will Make an Impact
Lead research efforts focused on engineering and discovery of viral vectors for gene therapy
Design and optimize molecular and cellular assays for high-throughput screening
Conduct viral vector development, transfection, transduction, and sequencing-based analysis
Build and characterize viral vector libraries using advanced molecular biology methods
Perform mammalian cell culture, primary cell work, and provide in vivo study design support
Prepare and analyze Next- Sequencing (NGS) libraries, with exposure to long-read sequencing (PacBio)
Document protocols, deliver reports, and present results to cross-disciplinary teams
Mentor junior scientists and support lab operations while maintaining high-quality standards
Are You an Accomplished Scientist Ready to Drive Innovation in Gene Therapy?
PhD in cell biology, virology, immunology, molecular biology, bioengineering, or related field with 2+ years of industry experience (academic considered), OR Master’s with 8+ years hands-on experience
Proven expertise in viral vectors; direct AAV experience strongly
Strong foundation in molecular biology (cloning, PCR/qPCR/ddPCR, DNA/RNA workflows)
Skilled in mammalian and primary cell culture
Background in viral vector engineering, library preparation, and screening
NGS sample preparation experience required; PacBio or long-read sequencing strongly desired
In vivo study design experience is a plus
Prior leadership or mentorship experience , with potential to transition into a leadership role after conversion
Strong communication, problem-solving, and organizational skills
#J-18808-Ljbffr