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2 дня назад

Associate Scientist II (Biotech)

Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Associate Scientist II (Biotech): Conducting cell-based and analytical assays for pharmaceutical and biotech research services with an accent on cell culture, laboratory automation, and assay data quality. Focus on developing and optimizing methods, analyzing and QC-reviewing data, and supporting R&D projects with minimal supervision.

Location: St. Charles, Missouri, United States; onsite laboratory work, Monday–Friday, 8:00am–5:00pm, with overtime as needed. Candidates must be authorized to work in the United States indefinitely without restriction or sponsorship and should live within commuting distance.

Salary: Not specified.

Company

International life sciences and analytical testing organization providing laboratory research and testing services across pharmaceutical, biotech, food, environmental, cosmetic, and other industries.

What you will do

  • Perform cell-based and analytical assays for ADME Toxicology, Ion Channel, Translational Biology, Cell and Gene Therapy, and Large Molecule Services.
  • Maintain cell cultures in a BSL2 laboratory using aseptic technique and cleanroom guidelines.
  • Prepare and manage buffers, reagents, media, inventory, and laboratory materials.
  • Conduct production assays using recombinant, primary, and traditional cell models.
  • Calculate and analyze data, perform QC reviews, and prepare project reports.
  • Support R&D projects, equipment maintenance, client communication, training, and cross-functional delivery with minimal supervision.

Requirements

  • Bachelor’s degree with at least 2 years of relevant experience, or master’s degree with at least 1 year of relevant experience.
  • Experience with in vitro enzymatic assays, HPLC, GC–mass spectrometry, ELISA, high-content imaging, electrophysiology, or flow cytometry.
  • Experience in a contract research organization and in GLP or cGMP laboratory services.
  • Experience with method development and optimization, automation, robotics, HTS applications, and recombinant cell-line development.
  • Experience with documentation, laboratory record-keeping, data management, equipment, and office software.
  • United States work authorization without restriction or sponsorship is required.

Culture & Benefits

  • Full-time employment with medical, dental, and vision coverage.
  • Life and disability insurance.
  • 401(k) with company match.
  • Paid vacation and holidays.
  • Collaborative laboratory environment with opportunities to train colleagues and contribute to research and development initiatives.

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