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5 дней назад

Manufacturing Project Engineer Intern (Manufacturing)

25$
Формат работы
onsite
Тип работы
fulltime
Грейд
trainee
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
Manufacturing Project Engineer Intern (Manufacturing) (Life Sciences Manufacturing): Supporting facility expansion, process equipment qualification, and production process development in a regulated life sciences facility with an accent on equipment studies, IQ/OQ protocols, and cGMP compliance. Focus on designing and executing qualification activities, analyzing safety and efficiency, and coordinating with engineering teams, suppliers, and external partners.

Location: Logan, Utah, United States

Salary: $25.00 per hour

Company

hirify.global’s Cytiva operates in the life sciences industry, developing products and solutions that support biological research, vaccines, medicines, and cell and gene therapies.

What you will do

  • Support facility expansion and process equipment qualification efforts.
  • Draft and execute equipment qualification studies, including sampling, data collection, and data compilation.
  • Create and execute IQ/OQ process equipment qualification protocols, engineering reports, and test protocols.
  • Organize equipment documentation such as design files, manufacturing drawings, P&IDs, manuals, spare parts lists, and maintenance schedules.
  • Evaluate equipment safety, quality, production performance, and cost efficiency while supporting capital expenditure priorities.
  • Collaborate with engineering disciplines, suppliers, third-party engineering services, and external partners to ensure designs meet intended-use requirements.

Requirements

  • Availability for the Summer 2027 internship from April through August.
  • Pursuing a bachelor’s degree in mechanical, industrial, manufacturing, or a related engineering or technical field.
  • Ability to apply scientific and engineering skills to evaluate and develop processes.
  • Excellent oral and written communication skills with the ability to work cross-functionally and independently.
  • Initiative, attention to detail, intellectual curiosity, and willingness to develop practical solutions to technical challenges.
  • Compliance with cGMP regulations, company policies, and ISO 13485-related quality requirements is expected.

Nice to have

  • Mechanical proficiency and hands-on machine design experience.

Culture & Benefits

  • Structured internship experience focused on professional skills, business acumen, feedback, and networking.
  • Cross-functional collaboration across electro-mechanical design, automation controls, facilities, quality, validation, and manufacturing.
  • Work on products and processes supporting life-saving research, medicines, and therapies.
  • Commitment to workplace and environmental safety, equal opportunity, and reasonable accommodations.

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