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Large-scale production: Independently carrying out filtration and chromatographic processes (250–1,000 litres) under GMP conditions...

• Preparation, review and approval of qualification documents for production equipment
• Conducting and documenting risk analyses at equipment level
• Initiating, processing and reviewing compliance activities such as non-conformities, CAPAs and CCOs

• Design, synthesize, and optimize bead-based materials for life science and diagnostic applications.
• Characterize bead properties using analytical, physicochemical, and material characterization techniques.

(Liquid Handling) Automation Specialist (80 – 100 %) Celerion is one of the world's leading bioanalytical contract research organizations and has been supporting pharmaceutical and biotech drug development programs around the world for more than 40 years. Due to the steady growth of our company and...