Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Крутая вакансия
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Чётко очерченная senior-роль в крупной биофармацевтической компании даёт возможность вести полный цикл переноса технологий и влиять на производство, но работа только на месте в Виспе ограничивает гибкость.
?Работа в Виспе
Широкая ответственность
Крупная биофарма
Помощь с переездом
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
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.
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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