R&D Upstream Scientist II
About The Position
The R&D Upstream Scientist II will work in a high-performing team to drive innovation in scalable viral vector production platforms for in vivo and ex vivo gene therapy applications. The role identifies, develops, and implements new and existing viral vector production technologies, with a focus on upstream bioprocessing, using internal and external resources to create robust, scalable solutions to viral production bottlenecks. This is a hands-on, fully site-based position in Houston, Texas. The scientist designs and executes experiments, develops metrics to evaluate results and technologies, and procures equipment. The role also acquires, analyzes, and communicates experimental data across functions. In-person collaboration supports the technical precision needed to manufacture medicines to high quality and safety standards.
Requirements
- Master's or Ph.D. degree in molecular virology, molecular biology, or chemical engineering.
- More than three years of industry experience, or relevant virus research experience in academia evidenced by peer-reviewed publications.
- Skills in bioprocessing, cell culture, viral vector production, transfection, Ambr15/250, and 3L bioreactors.
- Excellent oral and written English communication skills.
- Ability to work collaboratively as a team member and independently.
Responsibilities
- Lead a team developing next-generation viral production platforms, focusing on upstream platforms for gene therapy and contributing to pipeline development of novel, high-value vectors and bioprocessing methods.
- Independently design and execute experiments, analyze and communicate data, interpret results, and propose next steps.
- Obtain and analyze experimental data using statistics and graphing software.
- Maintain accurate, up-to-date records, including appropriate laboratory notebook entries, and deliver high-quality work on time.
- Present regular updates to the supervisor, R&D management, and process development teams, and present at technical meetings.
- Support evaluation of business development opportunities involving novel viral gene therapy platforms.
- Write and revise technical documents, including laboratory SOPs, test protocols, and reports.
- Participate in laboratory maintenance and procurement activities.
- Perform other duties as assigned.
Benefits
- Medical, dental, and vision insurance.
- Compensation programs that recognize high performance.
- An agile career and dynamic working culture.
- An inclusive and ethical workplace.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
