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9 дней назад

Teamlead Downstream Processing (Biotechnology)

Формат работы
onsite
Тип работы
fulltime
Грейд
lead
Английский
c1
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
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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