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3 часа назад

Scientist – Analytical Method & Stability (F/M/X) (Pharmaceutical Analytical Development)

Формат работы
remote (только Belgium)
Тип работы
fulltime
Грейд
junior
Английский
b2
Страна
Belgium
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
Scientist – Analytical Method & Stability (F/M/X) (Pharmaceutical Analytical Development): Supporting synthetic drug candidates from early development through commercialization by designing stability studies, developing analytical methods, and characterizing products with an accent on liquid chromatography and stability assessment. Focus on interpreting chromatographic data, validating and transferring methods, and aligning analytical strategies across development teams.

Location: Beerse, Belgium

Company

hirify.global is an independent technology consulting firm providing guidance and solutions across Information System & Digital, Telecom, Life Sciences, and Engineering.

What you will do

  • Support multiple synthetic development projects involving oligonucleotides, peptides, conjugates, and degraders.
  • Design and execute fit-for-purpose stability studies, including ICH stability, RIBPS, and open-dish stress studies.
  • Contribute to analytical method development, validation, and transfer, with a focus on liquid chromatography.
  • Interpret chromatographic and physicochemical data for product characterization and stability assessment.
  • Collaborate with Analytical Development, API, and Drug Product teams to align analytical strategies.
  • Prepare protocols, reports, data summaries, and other scientific documentation for project teams.

Requirements

  • PhD in Analytical Chemistry, Pharmaceutical Technology, or a related science with 0–3 years of experience, or a Master’s degree in Chemistry, Biochemistry, or a related field with at least 3 years of relevant experience.
  • Knowledge of stability studies for synthetic compounds, including ICH, RIBPS, and stress studies.
  • Experience with analytical method development, validation, and transfer, ideally using liquid chromatography.
  • Understanding of synthetic drug substances, formulations, conjugates, oligonucleotides, degraders, and related analytical techniques.
  • Ability to work independently and collaboratively, manage deadlines, and communicate scientific results clearly.

Nice to have

  • Industrial experience and familiarity with GMP.

Culture & Benefits

  • Long-term projects with major accounts and support from internal Centers of Excellence.
  • Structured project check-ins, management support, and regular HR communication.
  • Functional and geographic mobility across four areas of expertise and more than 60 countries.
  • Access to training modules and fully funded Microsoft certifications.
  • Health insurance, remote work options, meal vouchers, a time savings account, and a referral bonus.

Hiring process

  • Brief virtual or phone call.
  • Approximately three interviews with the line manager and other relevant team members.
  • Possible case study, technical assessment, role play, or problem-solving exercise.

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