Назад
Company hidden
6 дней назад

Principal Research Scientist II (Biotechnology)

141 500 - 268 500$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Principal Research Scientist II (Biotechnology): Leading the development, lifecycle management, troubleshooting, and commercialization of parenteral manufacturing processes with an accent on fill-finish technology, filling machines, process engineering, and cGMP requirements. Focus on designing process equipment and facilities, developing computational models, resolving manufacturing issues, and driving cross-functional technical initiatives.

Location: North Chicago, Illinois, United States

Salary: $141,500–$268,500 per year

Company

hirify.global develops medicines and solutions for serious health conditions across immunology, oncology, neuroscience, and aesthetics.

What you will do

  • Lead the development and lifecycle management of parenteral manufacturing processes from development through product launch and technical commercial support.
  • Provide technical expertise on filling machines, equipment capabilities, process design, and troubleshooting.
  • Guide development and manufacturing teams in resolving technical issues and implementing process improvements.
  • Support equipment selection and facility design for new or expanding manufacturing sites.
  • Develop and apply small-scale and computational process models for development projects.
  • Represent Parenteral PDS&T in cross-functional teams and present scientific results to diverse audiences.

Requirements

  • Master’s degree or diploma with 14+ years of experience, or PhD with 8+ years of experience, in parenteral manufacturing, process development, process engineering, product quality, analytical sciences, material sciences, or a related field.
  • Expert knowledge and practical experience in fill-finish technology, including machine technology, machine setup, mixing systems, and process development.
  • Strong knowledge of quality and regulatory requirements for parenteral pharmaceutical and biopharmaceutical processing and filling equipment.
  • Understanding of pharmaceutical development in a cGMP environment.
  • Demonstrated leadership in establishing and managing cross-functional manufacturing teams.
  • Strong problem-solving, organization, communication, and collaboration skills, including the ability to influence without direct authority.

Nice to have

  • Practical experience with parenteral fill-finish processes.

Culture & Benefits

  • Collaboration with global engineering, manufacturing, process development, quality, and external partner teams.
  • Opportunities to evaluate new technologies and lead global initiatives.
  • Paid vacation, holidays, and sick leave.
  • Medical, dental, and vision insurance.
  • 401(k) and eligibility for long-term incentive programs.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →