Your responsibilities

• Development, optimization and implementation of mRNA synthesis process for mRNA manufacturing.
• IVT template design, molecular cloning, plasmid multiplication in E.coli cultures
• Plasmid and mRNA quality control method and assay development, including PCR, qPCR, ELISA, spectrofluorometry
• Collaborating with other research and development teams (formulation team, analytics team, bioassay team) in a multidisciplinary environment
• Preparation of technical documents, such as method SOP, development reports, experimental plans and reports, scale-up documentation etc.
• Organization of data, maintaining detailed records, and effective communication of results
• Supervision of laboratory devices and equipment

Our requirements

• MSc in biology, biotechnology, biochemistry or related sciences with 3 years of professional experience; or PhD in above mentioned scientific fields. Industry experience is highly preferred
• Upstream and downstream mRNA process development knowledge
• Extensive knowledge and experience in molecular biology, specifically involving mRNA and molecular cloning, is required
• Experience with gene therapy products and/or mRNA vaccines is a plus
• Good understanding of mRNA biology and mRNA synthesis
• Experience in Pharmaceutical, CDMO, or cGMP environment preferred
• Good understanding of mRNA therapeutic area
• Very good knowledge of English, spoken and written
• Excellent oral and written communication skills
• Strong scientific skills including sound experimental design, data processing and interpretation
• Self-motivator with an ability to lead the project

What we offer

• Stable employment

• Employment contract

• Benefits under the Social Fund

• Subsidies for private medical care

• A sports card on attractive terms

• Life insurance on preferential terms