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Analytical Development Specialist
看过: 140
更新日: 16-11-2025
位置: Braine-l’Alleud Walloon Brabant
类别: 其他
行业:
水平: Entry level
工作类型: Full-time
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工作内容
SRG are working with a global biopharma company based in Belgium. Their ambition is to transform the lives of people living with severe diseases with a focus on neurology and immunology disorders - putting patients at the centre of their world.They are currently seeking an Analytical Development Specialist to join the team. The successful candidate will be responsible for validating analytical methods for quality control of medication and provide support to chemists and formulators. They will also participate in the release and stability analyses of raw materials, intermediates, drug substances or drug products.
Role Overview
Operational
- Validate analytical methods to support projects in development in different phases of product development.
- Perform analyses of raw materials, intermediate products, in bulk or packaged finished products in accordance with work instructions and established procedures (stabilities, in-process control, clinical release, investigation, ...).
- Ensure stability analyses and clinical release for clinical phases I and II, as well as any analyses in support to process understanding (IPC test, forced degradation study, multimedia dissolution, ...)
- Analyze results with readiness to criticize and ensures the consistency of these results with earlier data if relevant.
- Participate to analytical exercise transfer to QC and subcontractors.
- Read and Write in English
- Make sure to have received and understood all the information and instructions required for the tasks before starting work.
- Respects the procedures and reports any discrepancies to the responsible
- Use authorized and validated methods prior to testing, if applicable.
- Respect and properly maintain the analytical equipment and facilities at disposal.
- Performs double check the team
- Master/Bachelor/graduate A1: analytical chemistry
- Min years’ experience required: 2-3 years
- International experience desirable
- Key technical backgrounds: small molecule chromatography (HPLC/UHPLC/GC) and detection techniques (UV/Vis, MS), USP/EP Pharmacopoeias,
- Experience in LC-MS/MS (TripleQuad) is recommended
- Mandatory skills: team player, exp. in a similar position/environment, compliant/rigorous (understands the importance of following procedures in detail)
English: able to read/write scientific documents
French: mandatory/fluent
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最后期限: 31-12-2025
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