Analytical Development Analyst (Chromatography)

Randstad Belgium; Waals-Brabant; Sur place; EUR 45 000 - 65 000; Plein temps

Résumé du poste

Randstad Belgium is seeking two Analytical Development Analysts in Waals-Brabant to join a 35+ person lab advancing life-changing therapeutics. You will develop and validate analytical methods, ensure data integrity, and support transfers for early-phase development.

Requires 3–5+ years in pharma, strong HPLC/UPLC/GC skills, and fluent French with good English; team-oriented, rigorous, and compliant in a fast-paced environment.

Qualifications

• Bachelor’s degree in Analytical Chemistry or equivalent scientific field.
• 3 to 5+ years in a regulated pharmaceutical lab with autonomy.
• Strong proficiency in HPLC, UPLC, and GC with UV/Vis, RI, or MS detection.
• Fluent French (spoken/written) and good written English.
• Team-oriented, rigorous, quality-compliant, with strong communication skills.

Responsabilités

• Develop, validate, and optimize analytical methods for raw materials, intermediates, drug substances, and drug products across development and routine phases.
• Perform stability analyses, release testing, dissolution, forced degradation, and IPC testing for early-phase clinical development.
• Analyze complex data, ensure consistency, and support transfers to QC laboratories and external partners.
• Maintain strict compliance with procedures and document results with lab software, ensuring data integrity.

Connaissances

HPLC

UPLC

GC chromatography

Data interpretation

Communication skills

Team collaboration

French language

English language (written)

Formation

Bachelor’s degree in Analytical Chemistry or equivalent

Outils

HPLC systems

UV/Vis detectors

MS detection

Description du poste

Randstad Belgium is seeking two Analytical Development Analysts in Waals-Brabant to join a 35+ person lab advancing life-changing therapeutics. You will develop and validate analytical methods, ensure data integrity, and support transfers for early-phase development.

Requires 3–5+ years in pharma, strong HPLC/UPLC/GC skills, and fluent French with good English; team-oriented, rigorous, and compliant in a fast-paced environment.