5 дней назад
Manufacturing Project Engineer Intern (Manufacturing)
25$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
’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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