Supporting our Drug Product and Analytics development activities
In this role, you will play an important role in the development of drug product fill-finish manufacturing processes and in the development of analytical methods to assess critical quality attributes. We have adopted the ambitious standard of establishing robust analytical methods, formulations, and manufacturing processes ready for transfer into a cGMP-regulated environment. This role is highly cross-functional, and you will work in close collaboration with other research and development groups such as process development, developability assessment and pharmacology group. We are looking for a highly motivated and collaborative individual with a passion for data-driven development, who also enjoys working in a fast-paced, highly dynamic, and cross-functional working environment.
Key Responsibilities
Your Profile
Are you interested? For any further questions or your application please contact: wolfgang.kress@cdr-life.com. We are looking forward to hearing from you.
Wagistrasse 27, Schlieren, Switzerland