Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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В Company hidden чётко описана старшая роль в биофармацевтическом производстве с техническим лидерством и улучшением процессов; работа только на площадке и требование немецкого языка сужают круг подходящих вариантов.
?Только на площадке
Чёткая зона ответственности
Биотехнологии
Помощь с переездом
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Senior Bioprocess Engineer (Biotechnology Manufacturing): Providing technical leadership for GMP manufacturing campaigns and improving upstream and downstream bioprocesses with an accent on batch execution, process monitoring, risk assessment, and GMP documentation. Focus on troubleshooting production issues, implementing sustainable process and equipment improvements, and coaching manufacturing teams while supporting audits and inspections.
Location: Fully site-based in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families.
Company
hirify.global operates biotechnology manufacturing sites worldwide and develops manufacturing solutions for innovative therapies.
What you will do
Provide technical leadership and oversight for GMP manufacturing campaigns across upstream and downstream bioprocessing operations.
Support batch execution through data analysis, troubleshooting, process monitoring, and sustainable technical solutions.
Lead and review risk assessments and ensure follow-up actions are implemented and monitored.
Maintain high-quality GMP documentation and inspection-ready, compliant manufacturing processes.
Identify and implement improvements to processes, equipment, and workflows with Manufacturing, MSAT, Engineering, and Quality stakeholders.
Deliver product-specific training, coach colleagues, and act as a technical expert during audits, inspections, workshops, and cross-functional initiatives.
Requirements
Experience in pharmaceutical or biotechnology manufacturing environments with a strong understanding of GMP requirements and regulated operations.
Solid knowledge of biotechnological manufacturing processes, ideally including upstream processing, downstream processing, or both.
Experience with deviation investigations, risk assessments, process optimization, and GMP documentation.
Strong analytical and problem-solving skills, including sound technical decision-making in a fast-paced production environment.
Ability to collaborate across functions, influence stakeholders, and support technical leadership initiatives.
Fluency in German and English is required.
Degree in Biotechnology, Chemical Engineering, Bioinformatics, or a related scientific or technical discipline, or equivalent biopharmaceutical manufacturing experience.
Culture & Benefits
Agile career opportunities and a dynamic working culture.
Inclusive and ethical workplace focused on collaboration, accountability, excellence, passion, and integrity.
Performance-based compensation programs.
Benefits vary according to the role and location.
In-person collaboration supports real-time teamwork and the technical precision required for high-quality, safe medicine manufacturing.
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