Analytical Development Group Leader — GMP & Flex Hours

Ardena Careers

Gent

Sur place

EUR 90 000 - 120 000

Plein temps

Il y a 23 heures
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Avantages offerts par ce poste

Meal vouchers
Group health insurance
Hospitalization insurance
32 holidays
Flexible working hours

Résumé du poste

Ardena Gent is seeking an Associate Group Leader Analytical Development to guide a worldwide portfolio through formulation and analytical development, regulatory dossier prep, and the manufacturing of early-phase materials according to GMP standards. You will lead analytical method development, manage projects, and collaborate with engineering, QA, and clients.

The role demands a PhD or Master’s with relevant experience, strong chromatography and spectroscopy skills, and a proactive, AI-savvy

Qualifications

  • PhD or Master’s degree with 5 years of related experience in chemistry or pharmaceutical sciences.
  • Proven expertise in chromatographic methods (HPLC/UPLC/GC) and MS detection.
  • Experience with GMP environments; CMC method development is a plus.
  • Able to manage development projects independently within budget and timelines.
  • Strong analytical, reporting, and communication skills; team player; AI savvy.

Responsabilités

  • Lead analytical method development and GMP QC analysis as technical expert.
  • Translate customer goals into high-quality analytical methods.
  • Be the analytical expert in project team meetings.
  • Implement new analytical techniques in lab in collaboration with engineering.
  • Manage day-to-day activities of (Associate) Analytical Scientists.
  • Report to the Director Analytical Development.

Connaissances

Analytical method development
HPLC/UPLC/GC/MS
Spectroscopic techniques
GMP knowledge
Project management
Budget & timelines
Team collaboration
AI savviness

Formation

PhD or Master’s with 5y exp

Outils

MS Office
Empower

Description du poste

Ardena Gent is seeking an Associate Group Leader Analytical Development to guide a worldwide portfolio through formulation and analytical development, regulatory dossier prep, and the manufacturing of early-phase materials according to GMP standards. You will lead analytical method development, manage projects, and collaborate with engineering, QA, and clients.

The role demands a PhD or Master’s with relevant experience, strong chromatography and spectroscopy skills, and a proactive, AI-savvy

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