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11 дней назад

KBI: US - Scientist I (Cell-Based Assays)

86 000 - 115 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
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
KBI: US - Scientist I (Cell-Based Assays): Performing and interpreting bioassays, including 96-well cell-based assays and ELISAs, for contracted biopharmaceutical analytical programs with an accent on assay execution, data analysis, and cell culture. Focus on troubleshooting experiments, maintaining multiple cell lines without contamination, analyzing absorbance, luminescent, and fluorescent readouts, and meeting cGMP, GLP, and GCP documentation requirements.

Location: USA - NC - Durham - Hamlin Rd

Salary: $86,000–$115,000 per year

Company

hirify.global advances biopharmaceutical development and manufacturing to help life science companies bring medicines and vaccines to market.

What you will do

  • Perform and interpret bioassays, including cell-based assays and ELISAs, for contracted client analytical programs.
  • Execute 96-well cell-based assays with absorbance, luminescent, and fluorescent readouts.
  • Use plate readers, flow cytometers, and curve-fitting software to evaluate assay data.
  • Maintain multiple cell lines using aseptic technique, cell passaging, and cell banking while preventing contamination.
  • Conduct observations, elementary data analysis, troubleshooting, and experiment documentation.
  • Maintain instrumentation knowledge, scientific literature familiarity, laboratory notebooks, and safe handling of chemicals and hazardous waste.

Requirements

  • B.S. degree with 7 years of related experience, M.S. degree with 5 years of related experience, or Ph.D. in a scientific discipline.
  • Demonstrated expertise in cell-based assay analytical techniques.
  • Experience with plate readers, flow cytometers, curve-fitting software, aseptic technique, and cell culture.
  • Understanding of biotherapeutic regulatory requirements and expectations.
  • Strong oral communication, technical writing, presentation, and recordkeeping skills.
  • Ability to follow safety procedures and accurately document information required by cGMP, GLP, and GCP.

Culture & Benefits

  • Work in a highly technical analytical team within a dynamic biopharmaceutical development and manufacturing environment.
  • Participate in client-focused analytical programs with opportunities to contribute to project goals.
  • Follow established safety and health training requirements, including hazardous-waste handling.
  • Full-time employment in an on-site laboratory setting.

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