Requirements: English
Company: Randstad Professional Belgium
Region: Braine-l''Alleud , Wallonia
Location: Braine-lAlleud, Belgium (preferred)
Contract: project contract 6 months (with potential extension)
Your Key Responsibilities:
- Conduct bioanalytical method validation and sample analysis (PK, ADA, immunogenicity).
- Operate and maintain platforms: LC-MS, MSD, ELISA, PCR.
- Support assay transfer from method development teams.
- Ensure full GLP compliance, including documentation and audit readiness.
- Collaborate with Principal Investigators (PIs) and QA teams across various projects.
- Help improve and reshape our quality systems as we adopt new workflows.
Must-Haves:
- Minimum 23 years of hands-on lab experience in regulatory bioanalysis.
- Strong background in PK/ADA assays, preferably using MSD, LC-MS, or ELISA.
- Experience in a GLP/GCP-regulated environment.
- Masters degree in Life Sciences (or Bachelors with significant lab experience).
- Excellent communication and organizational skills.
- Fluency in English (spoken & written).
Nice-to-Haves:
- Knowledge of PCR, Watson LIMS, or statistical tools (GraphPad, JMP).
- Fluency in French is a major asset.
- Familiarity with QA interactions and compliance auditing.