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水平: Mid-Senior level
工作类型: Full-time
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工作内容
Make your mark for patientsWe are looking for a Senior Scientist Investigative Toxicology to join us in our organization based in Braine-l’Alleud, Belgium.About The Role- You will c ollaborate with project leaders to implement scientific technologies with minimal supervision to enhance productivity and efficiency within the Non-Clinical Safety function
- You will develop and/or implement novel assays based on organ-on-chip for in vitro toxicity/safety assessment
- You will design and execute predictive in vitro toxicity assays to support discovery and early development programs
- You will coordinate the analysis, interpretation, reporting, and archiving of data acquired
- You will be in charge of training of junior laboratory staff
- You will develop, optimize, and implement physiologically relevant organ-on-chip in vitro models, including providing technical expertise, design and execute qualification plans, and establish relevant endpoint assays to dissect the molecular mechanisms of toxicity
- You will focus on understanding the impact of UCB compounds on target organs toxicities according to the target organ strategies
- You will conduct in vitro experiments to identify potential liabilities in pre-clinical drug development
- You will design of experimental set-up, sample organization and preparation, data processing and analysis, reporting of the results
- You will ensure translation of strategy into hands-on lab work
- You will coach team members and help them with experimental setups ensuring adequate reporting of data and results
- You will guarantee proper experiment planning and execution, providing technical support when necessary
- You will communicate effectively and provide regular updates to team meetings to achieve high transparency, quality and traceability
- You will participate in the drafting of SOPs in order to be compliant with internal guidelines
- You will ensure correct and accurate documentation during operations, recording all experimental data and test results accurately and in the specified format
- You will establish, verify, validate and implement procedures and technical protocols
- You will independently review the literature to generate hypotheses for experimental testing. Design and coordinate the execution, analysis, and interpretation of relevant experiments to test hypotheses
- You will connect with CROs on outsourcing activities to optimize output regarding time, cost and quality
- You will connect to the outside community via consortia, collaborations, joint projects, chaired sessions, contribution to conferences and publications
- You will maintain current awareness of technology and theoretical development in the fields relevant to in vitro toxicology
- You have a PhD with at least 2 years post-doc experience
- You have demonstrated expertise in microphysiological systems/organ-on-chipapproaches with particular focus on characterizing toxico-pharmacological effect
- You have experience in working with a variety of in vitro cell model systems including primary cultures and iPSC-derived cells
- You have a profound interest in the execution of laboratory-based activities
- You have expertise in mammalian cell culture (primary, iPSC), imaging, molecular biology (RNA, DNA, protein) and biochemical endpoints (ELISA, MSD, qPCR, Capillary electrophoresis-based immuno-assay, Western Blot)
- You have some good interpersonal skills to communicate and maintain good working relationships within the team and with internal/external collaborators
- You have the ability to work independently in the experimental design and execution, data analysis, data interpretation and communication
- You have a high level of motivation, initiative, autonomy, flexibility with a result-oriented & problem-solving mindset
- You have excellent organizational and record keeping skills, capable of independently managing multiple projects in a fast-paced environment
- You have strong written communication skills for presenting and articulating experimental findings and conclusions to project teams and general audiences
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最后期限: 17-01-2026
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