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5 дней назад

Principal Scientist I, Chemistry

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

Текст:
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TL;DR
Principal Scientist I, Chemistry (Pharmaceutical Manufacturing Development): Conducting late-stage development and commercialization of small-molecule therapies through registration, manufacturing transfer, and product lifecycle activities with an accent on organic chemistry, process characterization, scale-up, and CMC documentation. Focus on designing laboratory experiments, leading cross-functional process development teams, solving complex manufacturing challenges, and supporting regulatory and commercial manufacturing strategies.

Location: North Chicago, Illinois, United States; onsite

Salary: $124,500–$236,500 per year

Company

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

What you will do

  • Lead or contribute to cross-functional teams developing manufacturing processes for small-molecule therapies.
  • Design and execute laboratory experiments supporting process development, characterization, scale-up, and commercial manufacturing.
  • Define project strategies, responsibilities, timelines, and scientific approaches.
  • Act as a subject-matter expert for manufacturing processes and collaborate with manufacturing, regulatory, quality, engineering, analytical chemistry, and solid-state science groups.
  • Author and review technical reports, batch records, CMC regulatory documents, publications, presentations, and patents.
  • Generate scientific proposals, evaluate emerging technologies and competitive developments, and mentor or supervise colleagues when needed.

Requirements

  • Bachelor’s degree with typically 14+ years of experience, master’s degree with typically 12+ years, or PhD with typically 6+ years in organic chemistry.
  • Experience in pharmaceutical manufacturing process development and scale-up.
  • Expertise in modern organic chemistry, mechanistic understanding, compound purification, and control strategy development.
  • Experience with standard analytical methods and tools including HPLC, UPLC, LC-MS, and NMR.
  • Demonstrated success in scientific communication, publications, presentations, or patent invention.
  • Strong collaboration, communication, and cross-functional leadership skills, with adherence to safety and GxP standards.

Culture & Benefits

  • Work in a cross-functional, matrixed environment focused on innovative medicines.
  • Collaborate across scientific, manufacturing, regulatory, and quality disciplines.
  • Operate within a learning-oriented environment that supports experimentation and innovation.
  • Follow corporate standards for safety, controlled materials, conduct, and GxP compliance.

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