R&D Upstream Scientist II (Viral Vector Production)
Контакты
Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
US
chemical engineeringmolecular biologybioprocessingcell culturebioreactorstransfectionmolecular virologyviral vector production
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Хорошая вакансия
развернуть
Роль чётко сфокусирована на разработке процессов производства вирусных векторов в крупной биофармацевтической компании, с практической R&D-работой и взаимодействием между командами; главный компромисс - работа полностью на площадке.
?Только на площадке
Понятные задачи
Вклад в генную терапию
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
R&D Upstream Scientist II (Viral Vector Production) (Bioprocessing/Gene Therapy): Developing scalable viral vector production platforms for in vivo and ex vivo gene therapy applications with an accent on upstream bioprocessing, cell culture, transfection, and bioreactor-based production. Focus on designing experiments, analyzing experimental data, solving viral production bottlenecks, and communicating results across R&D and process development teams.
Location: Houston, Texas, USA; fully site-based role
Company
hirify.global develops and manufactures medicines and bioprocessing solutions for pharmaceutical and biotechnology customers.
What you will do
Lead development of next-generation viral production platforms, focusing on upstream platforms for gene therapy and novel high-value vectors.
Design and execute experiments, analyze results with statistics and graphing software, define metrics, and propose next steps.
Acquire, analyze, document, and communicate experimental data across cross-functional R&D and process development teams.
Maintain accurate laboratory records and deliver high-quality results on time.
Present updates to supervisors, R&D management, process development teams, and technical meetings.
Write and revise laboratory SOPs, test protocols, and reports; support business development evaluations, laboratory maintenance, and equipment procurement.
Requirements
Master’s or Ph.D. degree in molecular virology, molecular biology, or chemical engineering.
More than three years of industry experience, or relevant academic virus research experience demonstrated by peer-reviewed publications.
Experience with bioprocessing, cell culture, viral vector production, and transfection.
Experience with Ambr15/250 and 3L bioreactors.
Excellent oral and written English communication skills.
Ability to work effectively both independently and as part of a team.
Culture & Benefits
Agile career and dynamic working culture.
Inclusive and ethical workplace focused on collaboration, ownership, learning, and problem-solving.
Medical, dental, and vision insurance.
Compensation programs recognizing high performance.
In-person collaboration supports technical precision and quality and safety standards for medicine manufacturing.
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