Research Associate I, Analytical Development (Biotech)
Контакты
67 000 - 73 700$
Формат работы
onsite
Тип работы
fulltime
Грейд
junior
Английский
b2
Страна
US
data analysisgmpbiotechnologyaseptic techniqueanalytical developmentcell culturewet chemistrybsl 2
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
Пожаловаться
Зарплата и рынок
Нижеразвернуть
$67к-74к/год
$68к$86кмедиана$110к
По похожим ролям (45) ~ $86к/год
74
Хорошая вакансия
развернуть
Понятные задачи начального уровня, практическая работа в биотехнологической разработке и хороший пакет льгот делают вакансию привлекательной для старта, но лабораторный формат на месте и быстрый темп подойдут не всем.
Ниже рынка
Понятные задачи
Перспективная биотехнология
Высокий темп работы
Хороший пакет льгот
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Подключить Plus
Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Research Associate I, Analytical Development (Biotech): Supporting analytical and process development for drug substance and drug product platforms with an accent on bench-scale experiments, product characterization, and BSL-2 laboratory work. Focus on preparing assays and solutions, interpreting experimental and manufacturing data, troubleshooting analytical methods, and maintaining GMP laboratory operations.
Location: On site in Louisville, Colorado, United States; Monday–Friday during standard business hours.
Annual base pay: $67,000–$73,700, depending on qualifications, experience, and geographic location. The position is also eligible for a discretionary bonus and equity award.
Company
hirify.global is a commercial-stage biotechnology company developing immunotherapies, cell therapies, cancer vaccines, and infectious-disease therapies designed to strengthen the natural immune response.
What you will do
Support process development for bench-scale upstream and downstream unit operations and multiple product platforms.
Assist with analytical method development, optimization, troubleshooting, qualification, validation, transfers, and feasibility testing.
Set up experiments, prepare buffers, solutions, and assay reagents, and collect and interpret experimental and manufacturing data under supervision.
Perform product-quality and characterization testing using UV-Vis, osmolality, pH, conductivity, Karl Fischer analysis, and other analytical chemistry techniques.
Maintain mammalian and bacterial cell cultures and conduct analyses involving BSL-2 microorganisms in a biological safety cabinet.
Document and trend data in laboratory notebooks, Excel, GraphPad Prism, or JMP; operate, clean, maintain, and calibrate laboratory equipment.
Requirements
Bachelor’s degree in biological sciences or biomedical engineering.
Basic aseptic or sterile-technique skills, wet chemistry knowledge, and laboratory best practices.
Computer skills and familiarity with Microsoft Word, Excel, and PowerPoint, together with strong technical writing skills.
Attention to detail, organization, critical thinking, troubleshooting, and problem-solving ability.
Good interpersonal, verbal, and written communication skills.
Ability to work productively in a fast-paced environment with minimal direction and changing priorities.
Ability to work on site in a GMP BSL-2 laboratory in Louisville, CO.
Ability to occasionally lift or carry up to 40 pounds and frequently bend, sit, and squat.
Nice to have
Experience in a research laboratory or regulated pharmaceutical environment.
Training in handling and maintaining mammalian cell cultures in a BSL-2 laboratory.
Training in data analysis.
Culture & Benefits
Collaborative work across Process Science, Manufacturing, Quality Assurance, Quality Control, and Process/Product Development teams.
Professional development opportunities in a growing, publicly traded biopharmaceutical company.
Medical, dental, and vision plan options; health and financial wellness programs; and an employer assistance program.
Life and disability insurance, flexible spending accounts, a 401(k) plan with company match, and a 529 education savings program.
Paid time off and holidays, with vacation and health-pay arrangements varying by exempt or non-exempt status.
Hiring process
The application window is anticipated to close 60 days after posting or earlier if the position is filled or closed.
Applications are reviewed and hiring decisions are made by human recruiters and hiring managers; AI tools are used only to assist with sourcing and outreach.
Будьте осторожны
Если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого. Это мошенники. Обязательно жмите «Пожаловаться» или пишите в поддержку. Подробнее в гайде →