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6 часов назад

Downstream Process Development Scientist II (Biotech)

106 480 - 146 410$
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
Downstream Process Development Scientist II (Biotech) (Chromatography and cGMP): Developing, characterizing, and transferring microbial downstream processes to commercial cGMP manufacturing with an accent on chromatography, tangential flow filtration, and regulatory-quality documentation. Focus on leading downstream development programs, optimizing unit operations, supporting technology transfer, and solving process and manufacturing issues.

Location: Boulder, Colorado, United States; onsite laboratory and manufacturing support, including shift coverage as needed.

Salary: $106,480–$146,410 per year

Company

hirify.global provides biopharmaceutical process development, technology transfer, and cGMP manufacturing services.

What you will do

  • Execute downstream process development, process characterization, and technology transfer for microbial processes.
  • Design and perform laboratory studies for chromatography, tangential flow filtration, normal filtration, sampling, and basic process-sample analysis.
  • Lead the downstream workstream for development, characterization, and technology transfer programs as a subject matter expert.
  • Prepare protocols, reports, client documentation, regulatory-quality records, and technical presentations.
  • Provide technical support during cGMP manufacturing through floor coverage, batch document review, deviation support, and change controls.
  • Evaluate and implement downstream technologies to improve process performance and operational efficiency.

Requirements

  • B.S. degree with 6+ years of related experience, M.S. with 4+ years, or Ph.D. with 1+ years in a scientific discipline.
  • Required experience in downstream process development and chromatography equipment.
  • Strong written and verbal communication skills, customer-service focus, and ability to meet strict client deadlines.
  • Collaborative approach and flexibility to support downstream processes and laboratory activities.
  • Ability to maintain training compliance and follow departmental safety procedures.
  • Knowledge of GMPs and regulations for biotechnology-derived products is preferred.

Culture & Benefits

  • Full-time salaried exempt employment.
  • Work includes collaboration across laboratory and manufacturing areas.
  • Workforce diversity and equal employment opportunity are supported.
  • Shift work may be required to meet laboratory and organizational needs.

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