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10 дней назад

Process Expert MSAT Downstream - Mammalian Large Scale (Biopharma Manufacturing)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Switzerland
Релокация
Switzerland
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 Expert MSAT Downstream - Mammalian Large Scale (Biopharma Manufacturing): Leading technology transfers, process scale-up, manufacturing implementation, and process troubleshooting for large-scale mammalian biopharma production with an accent on GMP compliance, process scalability, and cross-functional coordination. Focus on designing and implementing manufacturing processes, managing process risks and deviations, supporting capital projects, and driving continuous improvement.

Location: Visp, Switzerland. Relocation assistance is available for eligible candidates and their families.

Company

hirify.global is a global life sciences company developing and manufacturing products and services that support healthcare and biopharma applications.

What you will do

  • Lead cross-functional technology transfer projects from process design and scale-up through manufacturing implementation and completion.
  • Act as the interface between customers, process development, and operations, ensuring process scalability and manufacturability.
  • Manage process risks, change controls, deviations, regulatory requirements, and GMP risk analyses during manufacturing.
  • Support capital investment projects by delivering process inputs such as block-flow diagrams, media and buffer lists, and critical parameter lists.
  • Interact with customers during technology transfer and campaigns, including batch-status reporting, campaign preparation, execution, and closure.
  • Drive continuous improvement, standardized MSAT procedures, troubleshooting initiatives, technical documentation, staff training, and mentoring.

Requirements

  • Bachelor’s or master’s degree in biotechnology, chemical engineering, or a related discipline; PhD preferred.
  • At least 5 years of experience in biopharma manufacturing and/or process development, preferably in mammalian manufacturing.
  • Knowledge of GMP and a deep understanding of bioprocess technology.
  • Fluency in English is required.
  • Strong leadership, communication, teamwork, organization, and solution-oriented skills.
  • Ability to work with customers and multiple interfaces across project organizations.
  • Structured, focused, open-minded, agile, highly motivated, and dynamic working approach.

Nice to have

  • Fluency in German.

Culture & Benefits

  • Work in a global life sciences organization across five continents.
  • Opportunity to contribute to products and services that improve lives worldwide.
  • Ethical, people- and environment-focused working culture.
  • Relocation assistance for eligible candidates and their families.

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