In this position you will be responsible for quality control tasks in a GMP environment. You will test drugs in the laboratory for their use in clinical trials and at the same time you will work on the analytical development of our methods.

Your job profile includes:

• GMP analyses of clinical products for their release and stability studies
• Development and validation of analytical methods
• Release analyses of raw materials
• Troubleshooting for devices and methods
• Documentation of deviations and change requests
• Qualification, maintenance and calibration of laboratory equipment
• Interdepartmental project work

Your tasks and responsibilities in our young and dynamic start-up will be very diverse. As a prerequisite for this position, we expect a university degree in a relevant natural science (e.g. biochemistry, chemistry, pharmacy). You bring a high level of quality awareness and an analytical mindset to the team and have substantial experience with HPLC-based analytical methods. Experience in the GMP environment is considered a plus. You work independently, show initiative as well as team spirit and appreciate the dynamics of an innovative start-up company. Good communication skills and knowledge of English complete your profile.

Interested candidates are kindly requested to send their application documents to Ms. Melanie Bitterlin, who can also be contacted for additional information by phone or e-mail.