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7 дней назад

Bioprocess Engineer (m/w/d) 80%-100%

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
Bioprocess Engineer (GMP Bioprocessing): Planning, executing, and continuously improving GMP manufacturing campaigns for life-changing therapies with an accent on production documentation, deviation management, and qualified manufacturing operations. Focus on optimizing bioprocesses through Lean, Six Sigma, and Kaizen, troubleshooting equipment, and ensuring compliance across cleaning validation, environmental monitoring, and safety assessments.

Location: Visp, Switzerland. Fully site-based position; remote work is not available. Relocation support is available for eligible candidates and their families if required.

Company

hirify.global manufactures medicines across more than 30 sites on five continents and supports the development of viable therapies through collaboration, accountability, excellence, passion, integrity, and an inclusive work environment.

What you will do

  • Plan, execute, and document GMP manufacturing campaigns in collaboration with Operations leadership.
  • Provide technical and organizational support for GMP production, including training and coaching production personnel.
  • Create, optimize, and review production documentation, including EBRs, SOPs, and work instructions.
  • Handle deviations, change controls, and CAPAs in a timely, high-quality, first-time-right manner.
  • Monitor and improve operational KPIs using Lean, Six Sigma, Kaizen, and related continuous improvement methods.
  • Maintain qualified and technically compliant equipment and manufacturing areas, troubleshoot issues, participate in on-call rotations, optimize cleaning processes, and perform risk assessments.

Requirements

  • Bachelor’s or Master’s degree in Biotechnology, Bioprocess Engineering, Chemical Engineering, Life Sciences, or a related scientific or technical discipline.
  • Experience in a GMP-regulated environment within the biotechnology, pharmaceutical, or life sciences industry.
  • Strong knowledge of biotechnological manufacturing processes, GMP requirements, and documentation standards.
  • Experience with deviations, CAPAs, change controls, and risk assessments.
  • Excellent analytical skills, a structured and solution-oriented approach, and strong technical understanding.
  • Excellent English language skills and strong communication and teamwork abilities.

Nice to have

  • Experience with Operational Excellence, Lean Manufacturing, Six Sigma, or similar continuous improvement methodologies.

Culture & Benefits

  • Agile career path and dynamic working culture.
  • Inclusive and ethical work environment.
  • Compensation programs recognizing high performance.
  • Opportunities to shape and optimize complex GMP bioprocesses in an international, cross-functional environment.
  • Diverse development and training opportunities, with benefits supporting lifestyle, family, and leisure activities.

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