WHAT WILL YOU DO?

Your main focus will be executing laboratory- and cleanroom operations. This will also include supporting tasks such as documentation and planning. You will work in a small team on various projects, executing activities together with colleagues or individually.

YOUR TASKS INCLUDE:

• Hands-on work in the development laboratories and GMP Facility.
• Process development and Manufacturing of viral vectors and /or other cell- and gene therapy products/platforms and to support analytical development;
• Assist in process transfer from development to GMP production
• As needed, write and maintain SOPs and other manufacturing related documentation in alignment with applicable GxP guidelines;
• As needed, initiates and supports deviations investigations, Change Controls, CAPA’s, protocols and reports;
• Contribute to reports and work discussions;
• Support maintenance and upgrading of the development laboratories an/or cleanrooms equipment;
• Adheres to safety and GxP standards, continuously improves capabilities and keeps training status up-to-date.