Laboratory Scientist

Job Title: Laboratory Scientist

Contract Length: 6 Months - possible extension

Location: Braine-l'Alleud - Onsite (occasional remote work)

Salary: £55k-74k per annum

Hours: 40 hours, Monday to Friday

To strengthen our Regulated Bioanalysis, Precision Medicine team, we are looking for a talented individual to fill the position of: Scientist Regulatory Bioanalysis, based in Braine l’Alleud, Belgium (preferred)

As a Scientist Regulatory Bioanalysis, you will focus on supporting regulatory bioanalysis across our clients’ biologics portfolio.

You like to work in an environment where you can:

• 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

Interested? For this position you’ll need the following education, experience and skills:

Minimum Qualifications:

• 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
• English thorough knowledge, both spoken and written (French will be considered as a major advantage)

Specific skills. competences:

Bioanalysis

• Extensive hands-on laboratory experience in Bioanalytical validation and sample analysis
• Preferably good knowledgeable in PK, ADA
• Experience with MSD and ELISA platforms
• LC-MS/MS or PCR experience is a plus

Regulatory landscape coverage

• Extensive knowledge of GLP/GCP guidelines as applicable to bioanalysis
• Extensive knowledge of bioanalytical method validation guidelines

IT knowledge

• Experience using Watson LIMS or equivalent LIMS system
• Good knowledge of Microsoft Office
• Graphpad/JMP experience is plus

Others

• Very good communication skills
• Ability to work cross projects/supervisors
• Attention to detail and quality of work
• VERY well organized, able to function in a complex fast changing environment
• Team player
• Proactive