Назад
Company hidden
5 дней назад

Principal Research Scientist II (Parenteral Process Engineering)

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 (Parenteral Process Engineering): Developing and commercializing parenteral manufacturing processes with an accent on filling-machine technology, process engineering, equipment design, and cGMP requirements. Focus on troubleshooting manufacturing issues, developing small-scale and computational models, evaluating new technologies, and leading cross-functional technical initiatives.

Location: North Chicago, Illinois, United States; onsite role

Salary: $141,500–$268,500 USD per year

Company

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

What you will do

  • Provide advanced technical expertise in process engineering and troubleshooting for parenteral manufacturing processes.
  • Lead the development and lifecycle management of parenteral manufacturing processes from process design through commercialization and technical support.
  • Guide the selection and design of process equipment, including filling machines, mixing systems, and facilities for new or expanding manufacturing sites.
  • Provide technical guidance to development and manufacturing teams and lead the resolution of manufacturing issues.
  • Support process engineering projects through troubleshooting, small-scale modeling, computational modeling, and technology implementation.
  • Represent the parenteral PDS&T organization in cross-functional teams and drive global process improvement initiatives.

Requirements

  • Expert knowledge and practical experience in Fill & Finish technology, including machine technology, machine setup, mixing systems, and process development.
  • Profound knowledge of quality and regulatory requirements for parenteral pharmaceutical and biopharmaceutical processing and filling equipment.
  • Experience with parenteral manufacturing or process development and a solid understanding of pharmaceutical development in a cGMP environment.
  • M.Sc. or diploma with 14+ years of relevant experience, or PhD with 8+ years in parenteral manufacturing, process development, process engineering, product quality, analytical sciences, material sciences, or a related field.
  • Strong leadership, problem-solving, organizational, interpersonal, and technical communication skills.
  • Ability to work independently, manage changing priorities and short lead times, and influence multidisciplinary teams without direct authority.

Culture & Benefits

  • Collaboration with global engineering, manufacturing, process development, quality teams, and external partners.
  • Paid time off, including vacation, holidays, and sick leave, for eligible employees.
  • Medical, dental, and vision insurance for eligible employees.
  • 401(k) and eligibility to participate in 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 →