Job description:
We are looking for a full time senior analytical engineer to join and strengthen the QC team which consists of one scientist, 2 analytical engineers and 1 process technician.
The QC team is part of the larger GMP operations team consisting of a production team, QA managers, facility manager, application specialist, for a total of 20 colleagues.
You will be involved in the setup, validation and execution of QC methods for the analysis and release of ATMP products, to be used in clinical trials.
You will also take a leading role in deviation investigations and review of documentation. Experience of cell culture, flow cytometry, potency assays, ddPCR, qPCR, mycoplasma, sterility and endotoxin tests would be a significant asset; particularly in the context of ATMP analysis.
Knowledge of aseptic manufacturing techniques is desirable. Prior experience working in a GMP environment is essential for the role.
You must be capable of working as part of a team and demonstrate initiative to drive projects forward.
As the company and team is very international and the business language is English, excellent English communication skills is required.
The role is suited to experienced and motivated professionals with a drive to lead and execute by action.

Please refer the Job description for details