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6 дней назад

Manufacturing Line Specialist (Biopharmaceutical Manufacturing)

Формат работы
onsite
Тип работы
fulltime
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
Manufacturing Line Specialist (Biopharmaceutical Manufacturing): Supporting upstream or downstream manufacturing of life-changing biopharmaceutical products with an accent on cGMP compliance, process equipment troubleshooting, and manufacturing documentation. Focus on investigating deviations, change controls, and CAPA activities, commissioning equipment, and improving manufacturing operations in a regulated 4-shift environment.

Location: Visp, Switzerland; fully site-based role. Relocation assistance is available for eligible candidates and their families.

Company

hirify.global operates more than 30 sites across five continents and manufactures biopharmaceutical products for customers developing breakthrough therapies.

What you will do

  • Support upstream or downstream manufacturing activities in compliance with cGMP and safety requirements.
  • Troubleshoot process equipment, evaluate results, and recommend appropriate solutions.
  • Contribute to environmental monitoring, safety initiatives, and risk assessment activities.
  • Prepare, review, and maintain batch records, SOPs, and other manufacturing documentation.
  • Support investigations, deviations, change controls, and CAPA activities.
  • Participate in equipment commissioning, capital investment projects, and training for manufacturing personnel.

Requirements

  • Education in Biotechnology, Biology, Biochemical Engineering, or a related life sciences discipline.
  • Experience in biopharmaceutical manufacturing, including microbial or mammalian cell culture and/or protein purification.
  • Strong problem-solving, communication, teamwork, and collaboration skills.
  • Fluent English is required; German language skills are advantageous.
  • Understanding of GMP principles and pharmaceutical manufacturing practices.
  • Willingness to work in a 4-shift operation and attend the site in Visp.

Culture & Benefits

  • Agile career development and opportunities for professional growth.
  • Inclusive, ethical, collaborative, and supportive working environment.
  • Performance-based compensation programs and role-dependent benefits.
  • Relocation support for eligible candidates and their families.
  • Work focused on manufacturing medicines that can improve patients’ lives.

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