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3 дня назад

Principal Engineer I, Process Development (Pharmaceutical Development)

124 500 - 236 500$
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

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TL;DR
Principal Engineer I, Process Development (Pharmaceutical Development): Developing robust processes for late-stage small molecule solid dosage assets and commercial pharmaceutical products with an accent on process engineering, experimental design, and technical problem-solving. Focus on leading cross-functional studies, implementing new technologies, resolving complex engineering challenges, and preparing technical and regulatory documentation.

Location: North Chicago, Illinois, United States; site-based role.

Salary: $124,500–$236,500 per year.

Company

hirify.global develops innovative medicines and solutions across areas including immunology, oncology, neuroscience, and aesthetics.

What you will do

  • Lead cross-functional projects developing robust processes for late-stage small molecule solid dosage assets and commercial products.
  • Resolve complex engineering challenges and integrate scientific objectives into new or improved products and technologies.
  • Design and coordinate experiments, test hypotheses, and ensure experimental quality through sound study design.
  • Champion new technologies and develop technical alternatives based on literature, industry knowledge, and development experience.
  • Present complex technical data and author technical reports, documentation, and regulatory submissions.
  • Build scientific collaborations, share expertise, and mentor functional colleagues.

Requirements

  • Bachelor’s, master’s, or PhD in chemical engineering, mechanical engineering, bioengineering, pharmaceutical sciences, or a related field.
  • At least 14 years of related experience with a bachelor’s degree, 12 years with a master’s degree, or 6 years with a PhD.
  • Strong engineering background and deep technical expertise in pharmaceutical development.
  • Extensive experience with solid oral dosage process development in both laboratory and production environments.
  • Ability to solve complex technical problems, influence cross-functional collaborators, and build relationships across scientific disciplines.

Culture & Benefits

  • Paid time off, including vacation, holidays, and sick leave.
  • Medical, dental, and vision insurance for eligible employees.
  • 401(k) benefits for eligible employees.
  • Eligibility to participate in long-term incentive programs.
  • Equal opportunity employment focused on integrity, innovation, and community impact.

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