Analytical Development Analyst
Il y a 3 semaines
Brabant Walloon Region, GES, Belgique
Hays
Temps plein
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To join a leading pharmaceutical R&D environment and support the development of both small molecules and biological products from early development through commercialization, we are looking to recruit several
Analytical Development Analysts
.
Working within multidisciplinary analytical development teams, you will play a key role in method development, validation, transfer, and testing activities while collaborating closely with scientists, technicians, and cross-functional stakeholders.
Your Responsibilities
- Perform analytical testing of raw materials, intermediates, drug substances, and drug products.
- Design, develop, optimize, validate, and transfer analytical methods.
- Support stability studies and release testing activities.
- Analyze, interpret, and verify experimental data.
- Troubleshoot analytical and laboratory issues.
- Prepare, review, and contribute to protocols, analytical methods, and technical reports.
- Present and discuss results with project teams and stakeholders.
- Support analytical transfers to QC laboratories and external partners.
- Ensure compliance with GMP, HSE, and quality requirements. Technologies & Techniques You will work with a broad range of analytical techniques, including:
- HPLC / UPLC
- GC Chromatography
- UV/Vis, RI, and MS detection techniques
- Capillary Electrophoresis (CZE, CGE, iCE, MauriCE)
- Protein characterization techniques
- Chromatographic methods such as SEC, RP, IEX, Affinity, HILIC, and HIC
Your Profile
✅ Bachelor's or Master's degree in Analytical Chemistry, Biochemistry, or a related scientific field ✅ 3-5+ years of experience in a pharmaceutical, biotech, or analytical laboratory environment ✅ Strong experience in analytical method development, validation, and testing ✅ Hands-on expertise with chromatography and/or capillary electrophoresis techniques ✅ Ability to work autonomously in a laboratory environment ✅ Strong analytical, communication, and problem-solving skills ✅ Team-oriented mindset with a strong focus on quality and compliance ✅ Fluent French and good working knowledge of English Nice to Have
- Experience with Empower software
- Knowledge of USP / EP Pharmacopoeias
- Experience in analytical transfers
- Knowledge of GLP/GMP requirements
- Exposure to both chemistry and biologics development environments
- Experience with process understanding and validation activities Please apply on line
- Perform analytical testing of raw materials, intermediates, drug substances, and drug products.
- Design, develop, optimize, validate, and transfer analytical methods.
- Support stability studies and release testing activities.
- Analyze, interpret, and verify experimental data.
- Troubleshoot analytical and laboratory issues.
- Prepare, review, and contribute to protocols, analytical methods, and technical reports.
- Present and discuss results with project teams and stakeholders.
- Support analytical transfers to QC laboratories and external partners.
- Ensure compliance with GMP, HSE, and quality requirements. Technologies & Techniques You will work with a broad range of analytical techniques, including:
- HPLC / UPLC
- GC Chromatography
- UV/Vis, RI, and MS detection techniques
- Capillary Electrophoresis (CZE, CGE, iCE, MauriCE)
- Protein characterization techniques
- Chromatographic methods such as SEC, RP, IEX, Affinity, HILIC, and HIC
Your Profile
✅ Bachelor's or Master's degree in Analytical Chemistry, Biochemistry, or a related scientific field ✅ 3-5+ years of experience in a pharmaceutical, biotech, or analytical laboratory environment ✅ Strong experience in analytical method development, validation, and testing ✅ Hands-on expertise with chromatography and/or capillary electrophoresis techniques ✅ Ability to work autonomously in a laboratory environment ✅ Strong analytical, communication, and problem-solving skills ✅ Team-oriented mindset with a strong focus on quality and compliance ✅ Fluent French and good working knowledge of English Nice to Have
- Experience with Empower software
- Knowledge of USP / EP Pharmacopoeias
- Experience in analytical transfers
- Knowledge of GLP/GMP requirements
- Exposure to both chemistry and biologics development environments
- Experience with process understanding and validation activities Please apply on line