Tasks

- Participate in the development of manufacturing processes and the manufacturing of clinical trial materials
- Formulate the sterile dosage forms, write and modify SOPs
- Partaking in inprocess controls, investigations related to troubleshooting and the data compilation under cGMP
- Equipment cleaning/sterilisation and room cleaning for Class B and A areas

Qualifications

- Bachelor’s Degree in a related field is preferred, but not necessary
- At least 3 years of experience working as a Laboratory Technician in a sterile environment, under GMP regulations
- Experience in liquid filling
- Fluent in English, good knowledge of French or German is of advantage