Contractor Bioanalysis
Contracting – Brabant Wallon
Your responsibilities:
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
Your profile:
- 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
Our offer:
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, [email protected]
