This role will offer you:

• An opportunity to join one of the fastest growing Biotech companies in London and work on multiple manufacturing projects for AAV and Lentiviral vectors.
• Learning opportunities across the set up and running of a new manufacturing facility.

You will be responsible for:

• Aseptic operations within Grade A Cleanrooms.
• You will work on generation of GxP documents including MBRs, BOMs and SOPs.
• Reporting, investigation, and resolution of quality event.
• Perform batch data collection, analysis, and trending.
• Participation in validation activities.

You will bring the following:

• BSc, MSc or PhD in a Scientific or Engineering discipline along with GMP manufacturing experience for biopharmaceuticals.
• Experience in either upstream or downstream processing is essential.
• Knowledge or experience working with Viral Vectors would be highly desirable.