Your responsibilities

  • Designing and implementing innovative production processes.

  • Planning and execution of technology transfer from laboratory to production scale.

  • Performing synthesis and purification processes of mRNA and LNP.

  • Solving technological problems.

  • Creating and optimizing manufacturing processes.

  • Documenting the production process in accordance with GMP principles.

  • Working in accordance with the pharmaceutical quality system.

  • Operating and supervising production equipment.

  • Close cooperation with R&D and Quality departments.

Our requirements

  • Higher education – preferably in biotechnology, chemistry, biology or related fields.

  • Knowledge of cGMP principles and the specifics of working in the pharmaceutical/biotechnological industry.

  • Experience in working with preparative chromatography and/or ultra/diafiltration and/or mRNA synthesis – nice to have.

  • Good organization of work, communicability, and openness to new tasks.

  • English language at B2 level.

What we offer

  • Stable employment

  • Employment contract

  • Benefits under the Social Fund

  • Subsidies for private medical care

  • Sports card on attractive terms

  • Life insurance on preferential terms

We kindly ask you to add the following clause to your application: „I hereby express my consent to the processing of my personal data by SyVento Sp. z o. o. for the purpose of existing recruitment process”. If you want us to keep the submitted documents for the purposes of future recruitment processes, we kindly ask you to add the following clause to your application: „I hereby express my consent to the processing of my personal data by SyVento Sp. z o. o. for the purpose of future recruitment processes for a period of 3 years from the date of submission of this document, in order to analyse them in terms of the recruitment processes carried out in SyVento Sp. z o. o.”

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