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5 дней назад

QC Analyst / Data Reviewer (Biopharmaceuticals)

Формат работы
onsite
Тип работы
fulltime
Английский
c1
Страна
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
QC Analyst / Data Reviewer (Biopharmaceuticals): Conducting routine analysis and reviewing laboratory data for monoclonal antibody batches with an accent on HPLC, capillary electrophoresis, GMP compliance, and data integrity. Focus on investigating ambiguous results, managing instruments and consumables in gLIMS, and supporting timely batch release in a dynamic Quality Control laboratory.

Location: Visp, Switzerland

Company

hirify.global is a global life sciences company manufacturing medicines and supporting the development of biopharmaceutical therapies across more than 30 sites.

What you will do

  • Conduct routine analysis of biopharmaceuticals using HPLC and capillary electrophoresis.
  • Review HPLC and other laboratory raw data for accuracy, completeness, and compliance.
  • Use the gLIMS laboratory execution system to create consumable types and manage instruments and consumables.
  • Ensure laboratory activities comply with GMP requirements and internal procedures.
  • Investigate ambiguous results and adapt to changing priorities in the Quality Control environment.

Requirements

  • Completed training as a laboratory technician or a bachelor’s degree in chemistry, biochemistry, or a related scientific field.
  • Strong attention to detail, flexibility, and an investigative mindset.
  • Fluent English communication is required.
  • Experience in a GMP-regulated Quality Control environment is highly preferred.
  • Hands-on experience with HPLC and/or capillary electrophoresis is preferred.

Nice to have

  • German language skills.

Culture & Benefits

  • Agile scientific career in a dynamic GMP-regulated environment.
  • Inclusive and ethical workplace focused on collaboration and accountability.
  • Opportunities to deepen technical expertise and take ownership of impactful projects.
  • Cross-functional collaboration and interaction with regulatory stakeholders.
  • Competitive local benefits and support for continuous learning and improvement.

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