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9 дней назад

Process/Project Engineering Co-op (Biopharmaceutical Manufacturing)

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
Process/Project Engineering Co-op (Biopharmaceutical Manufacturing): Supporting the development of a large-molecule drug substance manufacturing site through process engineering documentation, commissioning and validation plans, data analysis, and project coordination with engineering teams and vendors. Focus on preparing SOPs and test plans, troubleshooting process systems and instrumentation, improving standards compliance, and tracking equipment, materials, and project activities.

Location: Wilson, North Carolina, United States; onsite

Company

Johnson & Johnson MedTech develops healthcare and biopharmaceutical solutions across Innovative Medicine and MedTech.

What you will do

  • Support the development of a new large-molecule drug substance manufacturing site.
  • Prepare engineering documentation, operating and maintenance procedures, SOPs, and commissioning and validation test plans.
  • Assist with testing, troubleshooting, and process improvement for utility systems, process systems, equipment, and instrumentation.
  • Develop tools to measure, track, and improve standards compliance and equipment utilization.
  • Pull, validate, and verify data; maintain databases, spreadsheets, project reports, and documentation.
  • Coordinate with project managers, engineering teams, internal functions, suppliers, and external vendors on schedules, procurement, inventory, and project activities.

Requirements

  • Currently pursuing a BS or MS in Chemical Engineering, Biomedical Engineering, Mechanical Engineering, Bioengineering, or a related engineering major.
  • Cumulative GPA of 2.8 or higher.
  • Strong analytical, organizational, time-management, communication, and problem-solving skills.
  • Proficiency with Microsoft Office, including Excel, Word, and PowerPoint.
  • Ability to work independently and collaboratively with minimal direction.
  • Must be permanently authorized to work in the United States without requiring current or future employment visa sponsorship.

Nice to have

  • Knowledge of large-molecule drug manufacturing and equipment such as bioreactors, chromatography, and tangential flow filtration.
  • Experience in a cGMP environment.
  • Understanding of monoclonal antibody production processes.

Culture & Benefits

  • Hands-on learning experience in biopharmaceutical manufacturing and process engineering.
  • Collaboration with process engineers, project engineers, team leads, and external vendors.
  • Opportunities to strengthen project management, communication, and engineering skills.
  • Professional networking and practical industry experience.
  • Inclusive work environment and equal employment opportunity.

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