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1 день назад

Principal Scientist, Synthetics Chromatography (LC/HRMS)

79 800 - 137 770
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Belgium
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

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TL;DR
Principal Scientist, Synthetics Chromatography (LC/HRMS): Developing and applying chromatographic and high-resolution mass spectrometry methods for active pharmaceutical ingredients, drug products, impurities, and degradation products with an accent on method development, validation, characterization, and stability testing. Focus on building digitally enabled analytical platforms, solving complex analytical challenges, and supporting synthetic drug development across peptides, conjugates, and degraders.

Location: Beerse, Antwerp, Belgium; onsite

Salary: €79,800–€137,770 annual base pay

Company

Johnson & Johnson Innovative Medicine develops pharmaceutical treatments and analytical solutions across the healthcare spectrum.

What you will do

  • Execute analytical experiments, including chromatographic method development, validation, product characterization, and stability testing.
  • Develop and apply liquid chromatography methods coupled with UV and mass spectrometry detection.
  • Use high-resolution mass spectrometry to analyze active pharmaceutical ingredients, drug products, impurities, and degradation products.
  • Initiate scientific ideas and technical opportunities for a digitally enabled analytical laboratory.
  • Manage multiple projects involving peptides, conjugates, degraders, and other synthetic modalities.
  • Collaborate with Analytical Development, API, and drug product development teams.

Requirements

  • PhD in Analytical Chemistry, Pharmaceutical Technology, or a related scientific field with at least 3 years of relevant experience, or a master’s degree in Chemistry, Biochemistry, or a related field with at least 7 years of relevant experience.
  • In-depth expertise in analytical method development and validation for R&D projects, with a major focus on LC-UV/MS.
  • Ability to oversee projects, set priorities, meet deadlines, and work with a sense of urgency.
  • Excellent communication skills and a proactive attitude.
  • Ability to adapt to a changing work environment and stay current with analytical technologies.

Nice to have

  • Knowledge or experience with the synthesis and drug formulation of small molecules, peptides, and degraders.

Culture & Benefits

  • Inclusive work environment focused on individual contribution, diversity, and dignity.
  • Annual bonus based on pay grade, location, and employee and company performance.
  • Vacation days, parental leave of at least 12 weeks, bereavement leave, caregiver leave, and volunteer leave.
  • Well-being reimbursement and financial, physical, and mental health programs.
  • Recognition awards and access to insurance plans subject to applicable terms.

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