Contractor Bioanalysis

Contracting – Brabant Wallon As a Scientist Regulatory Bioanalysis , you will focus on supporting regulatory bioanalysis across the company biologics portfolio. You will be responsible as a lab-based scientist for effective method validation and sample testing activities across multiple projects in the Immunology and CNS therapeutic portfolios You will contribute by: Supporting method validations and sample testing for PK and ADA assays delivering needs for pre-clinical and clinical studies Work with method development scientists for the successful transfer of assays. Maintenance of the GLP quality system as well as being involved in optimizing and reshaping the quality system as a function of new activities, /workflows being implemented Master's degree with a minimum of 2-3 years of experience as a Bioanalytical Scientist with a proven track record in method validation and sample Testing in support of bioanalytical study phases Preferably good knowledgeable in PK(LBA/LC-MS) and ADA analysis Experience working in regulatory environment (GLP/GCP) where the quality is paramount would be critical Fluency in French & English Experience with MSD and ELISA platforms LC-MS/MS or PCR experience is a plus Experience using Watson LIMS or equivalent LIMS system Good knowledge of Microsoft Office Graphpad/JMP experience is plus Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way. You're interested in this job? We kindly invite you to apply or send me your CV, lena.palmeri@jeffersonwells.be Method Development, CNS, VOS, Assays, Clinical Research, Platforms, Sample testing, LIMS, Maintenance, Multiple Project, Bioanalysis, Immunology, JMP, PCR, Biopharmaceuticals, Knowledgeable, Quality systems, Ada, Analysis, MS Office Suite, Transfer, Method validation, GLP

Location: eigenbrakel, BE

Posted Date: 5/12/2025