Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Чётко описанная руководящая роль в крупной компании из сферы наук о жизни даёт техническую ответственность и возможность развивать команду, но зарплата не указана, а работа полностью привязана к площадке в Виспе.
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Зарплата не указанаПонятная зона ответственностиКрупная биотех-компанияПомощь с переездом
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Teamlead Downstream Processing (Biotechnology): Leading the planning, execution, and documentation of biopharmaceutical downstream processing manufacturing campaigns with an accent on chromatography, filtration, UF/DF, GMP compliance, and process validation. Focus on managing investigations and continuous improvement, supporting technology transfers and start-up activities, and developing a team of Bioprocess Engineers.
Location: Visp, Switzerland; fully site-based role. Relocation assistance is available for eligible candidates and their families.
Company
hirify.global manufactures medicines and supports customers in turning life-science innovations into viable therapies across more than 30 sites worldwide.
What you will do
Lead the planning, execution, and documentation of downstream processing manufacturing campaigns.
Provide technical expertise in chromatography, filtration, UF/DF, bulk filling, process monitoring, technology transfers, validation, and lifecycle management.
Lead investigations, CAPAs, change controls, risk assessments, and continuous improvement initiatives.
Act as the downstream processing subject matter expert during audits, inspections, customer visits, capital projects, commissioning, qualification, and start-up activities.
Ensure manufacturing follows cGMP requirements, approved procedures, SHE standards, environmental monitoring, and quality requirements.
Lead, coach, and develop Bioprocess Engineers while partnering with downstream processing leadership and shift team leads on resource allocation, capacity planning, and manufacturing support.
Requirements
Bachelor’s or Master’s degree in Biotechnology, Biochemical Engineering, Chemical Engineering, Life Sciences, or a related field.
At least 5 years of experience in biotechnology, preferably in downstream processing operations.
Strong expertise in chromatography, filtration, UF/DF, viral clearance, and GMP-regulated manufacturing.
Experience with technology transfers, process validation, investigations, and continuous improvement.
Strong communication, stakeholder management, problem-solving, and people leadership skills.
Fluent English is required; German is highly desirable.
Culture & Benefits
Agile career development and a dynamic work culture.
Inclusive and ethical workplace.
Performance-oriented compensation programs.
Lifestyle, family, and leisure benefits tailored to the Visp location.
In-person collaboration in a site-based manufacturing environment.
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