Analytical Scientist
Il y a 2 jours
Antwerp Flemish Region, VLG, Belgique
Jefferson Wells Belgium
Temps plein
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Region of Antwerp
- Contracting For our client, specialized in the biopharmaceutical company, we are seeking an Analytical Scientist to join its Manufacturing Science, Analytics & Technology (MSAT) organization. This position offers the opportunity to play a key role in the development, transfer, validation, and continuous improvement of analytical methods supporting the manufacturing of innovative biologic therapies in a highly regulated GMP environment.
Key Responsibilities
- Act as the subject matter expert for qPCR and ELISA analytical methods.
- Lead the transfer of analytical methods from R&D to MSAT, ensuring effective documentation, training, and knowledge transfer.
- Support the transfer of validated qPCR and ELISA methods from MSAT to Quality Control (QC), including troubleshooting activities and preparation of transfer protocols and reports.
- Design, develop, optimize, and validate analytical methods for both existing and new manufacturing processes.
- Independently plan and execute analytical studies and experimental designs.
- Author high-quality scientific protocols, technical reports, and supporting documentation.
- Monitor method performance through data trending and statistical analysis to ensure reliability and robustness.
- Conduct root cause investigations related to analytical deviations and implement corrective actions where required.
- Present scientific findings and recommendations to cross-functional teams and stakeholders.
- Provide hands-on laboratory support for small-scale testing activities. Profile
- PhD or equivalent experience in Life Sciences, Biotechnology, Biochemistry, Molecular Biology , or a related scientific discipline.
- Strong practical expertise in qPCR and ELISA , ideally within a biopharmaceutical or biotechnology environment.
- Proven experience in analytical method development, qualification, and validation .
- Knowledge of protein characterization techniques such as SDS-PAGE , Western Blot , Southern Blot , or Northern Blot is considered an asset.
- Ability to design and execute Design of Experiments (DOE) studies and interpret complex analytical datasets.
- Strong statistical and data analysis skills, including method performance evaluation.
- Excellent problem-solving and troubleshooting abilities with a scientific and analytical mindset.
- Capable of managing multiple projects simultaneously while working independently.
- Comfortable balancing laboratory-based activities with documentation and data analysis tasks.
- Strong technical writing skills with experience preparing protocols, reports, and GMP documentation.
- Excellent understanding of cGMP requirements and their application to analytical methods and laboratory operations. Languages
- Fluent in Dutch and English , both written and spoken. Offer You will join a cutting-edge biopharmaceutical environment supporting the development and manufacture of next-generation biologic therapies. Working within an international and highly collaborative scientific team, you will contribute to analytical excellence, process innovation, and the successful delivery of life-changing medicines to patients worldwide.
- Contracting For our client, specialized in the biopharmaceutical company, we are seeking an Analytical Scientist to join its Manufacturing Science, Analytics & Technology (MSAT) organization. This position offers the opportunity to play a key role in the development, transfer, validation, and continuous improvement of analytical methods supporting the manufacturing of innovative biologic therapies in a highly regulated GMP environment.
Key Responsibilities
- Act as the subject matter expert for qPCR and ELISA analytical methods.
- Lead the transfer of analytical methods from R&D to MSAT, ensuring effective documentation, training, and knowledge transfer.
- Support the transfer of validated qPCR and ELISA methods from MSAT to Quality Control (QC), including troubleshooting activities and preparation of transfer protocols and reports.
- Design, develop, optimize, and validate analytical methods for both existing and new manufacturing processes.
- Independently plan and execute analytical studies and experimental designs.
- Author high-quality scientific protocols, technical reports, and supporting documentation.
- Monitor method performance through data trending and statistical analysis to ensure reliability and robustness.
- Conduct root cause investigations related to analytical deviations and implement corrective actions where required.
- Present scientific findings and recommendations to cross-functional teams and stakeholders.
- Provide hands-on laboratory support for small-scale testing activities. Profile
- PhD or equivalent experience in Life Sciences, Biotechnology, Biochemistry, Molecular Biology , or a related scientific discipline.
- Strong practical expertise in qPCR and ELISA , ideally within a biopharmaceutical or biotechnology environment.
- Proven experience in analytical method development, qualification, and validation .
- Knowledge of protein characterization techniques such as SDS-PAGE , Western Blot , Southern Blot , or Northern Blot is considered an asset.
- Ability to design and execute Design of Experiments (DOE) studies and interpret complex analytical datasets.
- Strong statistical and data analysis skills, including method performance evaluation.
- Excellent problem-solving and troubleshooting abilities with a scientific and analytical mindset.
- Capable of managing multiple projects simultaneously while working independently.
- Comfortable balancing laboratory-based activities with documentation and data analysis tasks.
- Strong technical writing skills with experience preparing protocols, reports, and GMP documentation.
- Excellent understanding of cGMP requirements and their application to analytical methods and laboratory operations. Languages
- Fluent in Dutch and English , both written and spoken. Offer You will join a cutting-edge biopharmaceutical environment supporting the development and manufacture of next-generation biologic therapies. Working within an international and highly collaborative scientific team, you will contribute to analytical excellence, process innovation, and the successful delivery of life-changing medicines to patients worldwide.