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Scientist I, Biologics Outsourcing Specialist (Biologics)

75 000 - 142 500$
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
Scientist I, Biologics Outsourcing Specialist (Biologics): Coordinating outsourced therapeutic biologics production at CROs from expression and purification through analytical QC, with an accent on protein production strategy, vendor collaboration, and data tracking. Focus on solving challenging production problems, aligning vendor QC methods, and interpreting rigorous analytical results across high-volume outsourcing projects.

Location: North Chicago, Illinois, United States; onsite position

Salary: $75,000–$142,500 per year

Company

hirify.global discovers and delivers medicines and solutions for serious health issues across areas including immunology, oncology, neuroscience, and aesthetics.

What you will do

  • Coordinate and manage outsourced therapeutic biologics production at CROs, covering requests from 100 mg to 50 grams.
  • Manage protein production activities including sequence design, expression method, scale selection, primary capture, secondary purification, and quality control.
  • Plan outsourcing projects, design strategies, manage risks, and track project status with requestors and collaborators.
  • Develop vendor data-sharing workflows and support accurate transfer of project data into LIMS.
  • Perform biophysical characterization and analytical QC, including SEC, intact and reduced mass spectrometry, endotoxin, and HCP testing.
  • Resolve scientific problems, communicate unexpected findings, and analyze and report experimental data.

Requirements

  • Onsite work in North Chicago, Illinois, United States is required.
  • Bachelor's or master's degree in biology, chemistry, biochemistry, or a related field, with typically 5+ years of experience for a bachelor's degree or 2+ years for a master's degree.
  • Experience with biologics production, including plasmid design, stable and transient CHO cell expression, Protein A, CH1, kappa select, AEX, CEX, and HIC purification.
  • Experience working with CROs on protein production projects.
  • Experience with analytical QC of biologics, including SEC, intact and reduced mass spectrometry, endotoxin and HCP testing, peptide mapping, released glycan analysis, and CE-SDS.
  • Experience in process development and optimization, including expression optimization and purification process development.

Culture & Benefits

  • Work supports worldwide drug discovery efforts and the development of therapeutic biologics.
  • Benefits include paid vacation, holidays, sick leave, medical, dental, and vision insurance, and a 401(k) for eligible employees.
  • Eligibility to participate in short-term incentive programs.
  • Collaboration with internal colleagues, external partners, and CRO vendors.

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