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Gene Therapy PCMD (Senior) Scientist
Ver: 165
Dia de atualização: 13-11-2025
Localização: Braine-l’Alleud Walloon Brabant
Categoria: Ciência Planejamento / Projetos
Indústria: Pharmaceutical Manufacturing
Posição: Mid-Senior level
Tipo de empregos: Full-time
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Conteúdo do emprego
Make your mark for patientsWe are looking for a Gene Therapy Physico-Chemical Method Development (Senior) Scientist who is team and solutions oriented to join us in our CMC Gene Therapy Analytical Development team, based in Braine-l’Alleud, BelgiumAbout The RoleThe 2 main objectives of the Gene Therapy (GT) Physico-Chemical Method Development (Senior) Scientist are:- To identify and to implement high throughput analytical tools supporting the release and stability of multiple therapeutic gene therapy programs throughout clinical phases (from phase 1 to readiness to launch).
- To develop, validate, tech transfer (to internal or external partners) and execute fast and reliable physico-chemical assays to support the clinical development of AAV-based Gene Therapy Products in accordance with current rules and procedures ( e. GMP/GSP)
- Michel Degueldre as your Manager and other amazing colleagues at transversal and global level.
- Support release and stability testing of Gene Therapy Products by developing, validating, coordinating, executing and/or tech transferring fast, reliable and QC friendly physico‑chemical assays.
- Contribute and potentially lead assay development, drive results.
- Cross-train and provide support for upstream/downstream operations, in-process analysis, characterization and vector biology teams ( e. Vector Core, Boston).
- Provide high quality documentation (procedures, protocols, reports) of all technical work performed in the lab in accordance with data integrity requirements.
- Verify data (double check, data check).
- Participate to the result analysis and trending.
- Present/discuss results in team meetings.
- Prepare written procedures and instructions.
- Sustain scientifically current (state of the art) laboratory environment and/or data systems.
- Work independently and cross functionally across various UCB teams related to analytical activities.
- Manage priorities and engage/communicate in a multidisciplinary environment. Support the development of the UCB GT strategy internally as well as externally ( e. CMOs/CROs).
- Master’s degree preferred in Analytical Chemistry, Biochemistry or equivalent with at least 3 years of professional experience within the biopharmaceutical industry.
- Previous development and validation of methods experience is mandatory; for viral vector products is a plus.
- Ability to operate the following techniques: capillary electrophoresis and/or liquid chromatography and/or dynamic and static light scattering.
- Strong and proven laboratory and statistical skills.
- Strong and proven experience in a regulated laboratory environment ( g. GLP/GMP).
- Strong and proven expertise in physico-chemical method development with hands-on experience developing biophysical based methods for viral vectors, protein or impurity quantification.
- Deep understanding of characteristics to be considered for the validation of the most common types of analytical methods.
- Mastering statistical tools supporting the development of analytical methods. Knowledge of total error approach is a plus.
- Mastering regulatory requirements and HSE/Biosafety rules.
- Good knowledge of English and ability to read, analyze, and interpret common scientific journals.
- Ability to think critically and demonstrate troubleshooting and problem-solving skills (identify problems, collect and analyze data, establish facts, and draw valid conclusions).
- Well organized, flexible, meticulous and rigorous (data integrity oriented).
- Ability to integrate new concepts and to work in a multicultural environment as well as to adopt an efficient and independent way of working in a changing environment.
- Interpersonal skills to communicate and maintain good working relationships within the team and with internal/external customers/partners.
- Team spirit oriented and able to offer/receive constructive feedbacks.
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Data limite: 28-12-2025
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