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4 дня назад

Emerging Technologies MSAT DS Biotherapeutics Fellow

164 000 - 278 800$
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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Текст:
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TL;DR
Emerging Technologies MSAT DS Biotherapeutics Fellow (Biotherapeutic Manufacturing): Shaping advanced manufacturing solutions for biotherapeutic drug substance processes with an accent on process intensification, real-time release, and process reliability. Focus on scouting and implementing emerging technologies, executing laboratory and pilot-scale studies, mentoring technical teams, and building partnerships across academia, government, and industry.

Location: Spring House, Pennsylvania, United States of America; full-time onsite role with up to 20% domestic and international travel.

Base pay range: $164,000–$278,800 per year.

Company

Global healthcare organization developing medicines, MedTech solutions, and other healthcare innovations.

What you will do

  • Shape the strategic direction of advanced manufacturing solutions for biotherapeutic drug substance processes.
  • Scout and benchmark emerging technologies supporting process intensification and real-time release.
  • Identify high-impact technologies and guide their laboratory and pilot-scale evaluation toward adoption.
  • Build and maintain relationships with academic, government, commercial, and internal partners.
  • Mentor technical contributors and support the Emerging Technologies organization’s advanced manufacturing roadmap.
  • Contribute to new or improved processes and products through technology discovery and licensing.

Requirements

  • BA/BS or PhD in chemical engineering, bioengineering, biomedical engineering, chemistry, or a related quantitative scientific field.
  • PhD holders must have 10–12 years of relevant experience.
  • Outstanding record of delivering strategic solutions for next-generation biotherapeutic pharmaceutical manufacturing.
  • Significant expertise in biotherapeutic or parenteral drug substance processes, unit operations, and GxP impacts.
  • Strong scientific communication skills, including authoring white papers and publications and presenting quantitative information visually.
  • Proficient written and spoken English required; up to 20% domestic and international travel required.

Nice to have

  • Knowledge of Quality by Design and pharmaceutical real-time release testing.
  • Familiarity with cGMP, systems qualification, process validation, tech transfer, PAT, continuous manufacturing, and modular manufacturing.
  • Experience with chemometric, mechanistic, machine learning, or AI-based modeling.
  • External scientific influence through presentations, publications, white papers, and academic or industry networks.

Culture & Benefits

  • Inclusive work environment focused on individual dignity, diversity, and employee wellbeing.
  • Vacation, sick time, holiday pay, parental leave, caregiver leave, volunteer leave, and military spouse time-off benefits.
  • Work focused on developing treatments, finding cures, and advancing healthcare innovation.

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