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4 дня назад

Sr. Associate Scientist, Analytical-ELISA/ddPCR (Contract) (Biotech)

45 - 50$
Формат работы
onsite
Тип работы
project
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Мэтч & Сопровод

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Описание вакансии

Текст:
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TL;DR
Sr. Associate Scientist, Analytical-ELISA/ddPCR (Contract) (Biotech): Developing and executing analytical methods for characterization, impurity testing, and release of clinical-scale allogeneic CAR T-cell products with an accent on ELISA, ddPCR, qPCR, and mammalian cell processing. Focus on method qualification, process characterization, tech transfer, GMP manufacturing support, and preparing data and documentation for regulatory filings.

Location: South San Francisco, California, United States; onsite

Salary: $45–$50 per hour

Company

hirify.global is a clinical-stage biotechnology company developing allogeneic CAR T-cell products for cancer and autoimmune disease.

What you will do

  • Develop and qualify analytical methods for CAR T-cell products.
  • Perform drug product characterization and impurity testing.
  • Support process characterization, BLA-enabling activities, in-process and release method qualification, and technology transfer.
  • Provide analytical support for GMP manufacturing and release of clinical material.
  • Document results in electronic laboratory notebooks and technical reports supporting regulatory filings.
  • Present data and analytical strategies to scientists and management.

Requirements

  • Bachelor’s or master’s degree in immunology, molecular biology, or a related field, or relevant experience.
  • Laboratory experience with nucleic acid extraction, qPCR, ddPCR, western blot, and ELISA.
  • Hands-on experience handling and processing mammalian cells.
  • Strong organizational, prioritization, communication, and interpersonal skills.
  • Ability to work independently and collaboratively.
  • Must be authorized to work in the United States.

Nice to have

  • Proficiency in data analysis and interpretation.
  • Familiarity with cGMPs and relevant regulatory guidance documents.

Culture & Benefits

  • Collaborative environment with cross-functional technical teams.
  • One-year contract opportunity with possible extension or contract-to-hire.
  • Opportunity to contribute to the development of clinical-scale cell therapies.

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