Biotech Method Development Analyst

Akkodis; Waals-Brabant; Sur place; EUR 55 000 - 75 000; Plein temps

Avantages offerts par ce poste

Permanent contract

Competitive salary package with extra-

Buddy onboarding

Career development

Résumé du poste

Akkodis is seeking a Development Analyst in Belgium to lead physico-chemical method development for Biologicals products from early clinical phases to commercial. You will work with LC and capillary electrophoresis techniques to develop and validate analytical methods.

You will autonomously manage daily lab activities, contribute to release/testing, and author procedures and reports while ensuring GLP/GMP compliance and strong English communication within a matrix organization.

Qualifications

• Master's or Bachelor's degree in biochemistry or analytical chemistry.
• Proven expertise preferably in biotech industry.
• Strong laboratory skills and good knowledge of protein chemistry.
• Experience with analytical techniques: chromatography or electrophoresis.
• Expertise in analytical method development and validation.
• Autonomy in day-to-day work and ability to write/ review procedures.
• Knowledge of GLP/GMP is a plus and English reports are recommended.

Responsabilités

• Autonomously manage and perform daily lab activities related to method development, validation, transfers.
• Contribute to release and stability testing related to the project.
• Prepare and review/approve documentation (procedures, protocols, reports).
• Analyze results and present them in project team meetings.

Connaissances

Biochemistry

Analytical chemistry

Laboratory skills

Protein chemistry

GLP/GMP knowledge

English communication

Formation

Bachelor's degree in biochemistry

Bachelor's degree in analytical chemistry

Outils

Chromatography

Capillary electrophoresis

Description du poste

Akkodis is seeking a Development Analyst in Belgium to lead physico-chemical method development for Biologicals products from early clinical phases to commercial. You will work with LC and capillary electrophoresis techniques to develop and validate analytical methods.

You will autonomously manage daily lab activities, contribute to release/testing, and author procedures and reports while ensuring GLP/GMP compliance and strong English communication within a matrix organization.