Analytical Scientist: LC/IC/GC Method Development

AMARIS GROUP SA

Beerse

Sur place

EUR 45 000 - 65 000

Plein temps

Il y a 20 heures
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Avantages offerts par ce poste

Health insurance
Remote work
Meal vouchers
Time savings account
Referral bonus

Résumé du poste

AMARIS GROUP SA in Belgium seeks an Associate Scientist to provide analytical support for new molecular entities from Phase 1 through registration, with a focus on LC, IC, and GC analyses. You will develop fit-for-purpose methods and ensure data quality under GMP guidelines.

In this role you will evaluate results, support method validation, and collaborate with cross-functional teams to enable timely progression of programs while upholding high scientific standards and regulatory compliance.

Qualifications

  • Master’s degree or equivalent with relevant experience in analytical chemistry.
  • Strong LC/IC/GC knowledge and hands-on experience.
  • Familiarity with CDS platforms and chromatographic data handling.

Responsabilités

  • Perform analyses for reference standard characterization focusing on LC/IC/GC.
  • Develop fit-for-purpose LC/IC/GC methods to meet LLRT for purity determination.
  • Support product and process characterization, method development, validation, release, and stability (LC focus).
  • Ensure compliance with regulatory guidelines, methods, GMP, and safety standards.
  • Conduct scientific evaluations of results.

Connaissances

LC/IC/GC analytics
Analytical method development
Regulatory compliance awareness
CDS systems: Empower/OpenLab
Accountability for data quality
Adaptability & priority management

Formation

Master’s degree in Chemistry, Pharmaceutical Sciences, Biochemistry or related field
Bachelor’s degree with relevant experience

Outils

Empower
OpenLab

Description du poste

AMARIS GROUP SA in Belgium seeks an Associate Scientist to provide analytical support for new molecular entities from Phase 1 through registration, with a focus on LC, IC, and GC analyses. You will develop fit-for-purpose methods and ensure data quality under GMP guidelines.

In this role you will evaluate results, support method validation, and collaborate with cross-functional teams to enable timely progression of programs while upholding high scientific standards and regulatory compliance.

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