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Intern (Pharmaceutical Manufacturing)

Формат работы
onsite
Тип работы
fulltime
Грейд
trainee
Английский
b2
Страна
Singapore
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Мэтч & Сопровод

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Описание вакансии

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TL;DR

Intern (Pharmaceutical Manufacturing): Supporting fill-and-finish pharmaceutical manufacturing operations with an accent on cGMP compliance, documentation, and process learning. Focus on troubleshooting process-related issues, developing standard operating procedures, and building problem-solving skills in a supervised manufacturing environment.

Location: Onsite at the Tuas facility in Singapore

Company

A global life sciences manufacturing organization with more than 30 sites across five continents, focused on turning customers’ innovations into viable therapies.

What you will do

  • Learn the principles and processes involved in pharmaceutical fill-and-finish operations.
  • Support manufacturing, quality, development services, and manufacturing science and technology teams in daily operations.
  • Follow cGMP and safety requirements during all activities.
  • Contribute to developing standard operating procedures in line with company policies.
  • Collaborate with colleagues to identify and troubleshoot process-related issues.
  • Organize tasks and maintain accurate documentation with daily supervision and coaching.

Requirements

  • Currently pursuing a degree in biomedical science, pharmaceutical science, biotechnology, chemical engineering, or a related field.
  • Strong analytical and problem-solving skills.
  • Excellent communication and interpersonal skills.
  • Ability to work independently and collaboratively.
  • Proficiency in Microsoft Office Suite and other relevant software.
  • Motivation to learn new processes and develop decision-making skills.

Culture & Benefits

  • Inclusive and ethical workplace.
  • Daily company bus service from an MRT location near home to the Tuas site and back.
  • Step-by-step guidance for new tasks and daily supervision for routine work.
  • Coaching on process flow in a cGMP manufacturing environment.
  • Collaborative culture focused on accountability, excellence, passion, integrity, and inclusion.

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