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10 дней назад

Senior Scientist DSP

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Switzerland
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

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TL;DR
Senior Scientist DSP (Biopharmaceutical Manufacturing): Leading downstream process technology transfers and introducing new products at the Yverdon Bioplant with an accent on GMP manufacturing, facility fit assessments, process modeling, and manufacturing support. Focus on troubleshooting complex process issues, validating processes, managing deviations, and driving cross-functional process improvements.

Location: Yverdon-les-Bains, Switzerland

Company

Biopharmaceutical manufacturing organization operating a production site in Yverdon-les-Bains.

What you will do

  • Lead downstream process technology transfers and new product introductions at the Yverdon Bioplant.
  • Assess facility fit, scalability, equipment capability, and operational readiness for incoming processes.
  • Provide downstream process expertise during GMP manufacturing campaigns and troubleshoot complex technical issues.
  • Lead or support GMP investigations, deviation reviews, process validation, and continued process verification.
  • Maintain process descriptions, MES master data, batch record configurations, and technology transfer documentation.
  • Drive process improvements that increase robustness, improve capacity, or reduce cost of goods.

Requirements

  • MSc or equivalent degree in biotechnology, biochemistry, chemical engineering, pharmaceutical sciences, or a related scientific discipline.
  • Significant experience in biopharmaceutical manufacturing, MSAT, process development, or technology transfer, preferably with downstream processing in a GMP environment.
  • Strong expertise in downstream manufacturing processes, associated equipment, GMP requirements, and regulatory expectations.
  • Experience with statistical tools and data analysis, including DOE and multifactorial analysis.
  • Experience with risk assessment methodologies such as FMEA and with investigations, change controls, validation documentation, and process performance assessments.
  • Ability to lead cross-functional troubleshooting and collaborate with Production, QA, QC, Engineering, and Process Science.

Culture & Benefits

  • Cross-functional collaboration with Production, Global Process Science, QA, QC, Engineering, and other stakeholders.
  • Interaction with Global Process Science teams in Yverdon and the United States.
  • Focus on compliance, business integrity, ethical behavior, and scientifically sound manufacturing.

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