In this role, the Scientist (m / f / d) will perform release and stability testing of clinical batches and act as the interface between method development and validation. The candidate will be responsible for performing the following tasks :
- Establishing and running chromatography (HPLC / UPLC) methods for release & stability testing of Biologics
- Documenting lab procedures work following cGMPs
- Performing method validation experiments according to approved protocols
- Authoring methods and technical protocols and reports
- Maintaining and calibrating analytical equipment following cGMPs
- Improving methods and troubleshooting around equipment and procedures
In order to be considered for the role, the selected candidate must have :
Master's degree in Biochemistry / Chemistry / Pharmaceutics / Biological Sciences or similar field, OR Bachelor's degree / Laboratory Technician EFZ with 3+ years of industry experience.Deep knowledge of protein biochemistry and hands on experience with analytical testing by HPLC / UPLC methods, e.g. Size Exclusion, Ion Exchange, Reverse Phase, HIC.Detailed knowledge of a relevant CDS (e.g. Empower)Ability to pipette small volumes precisely and prepare large number of samples.High attention to accuracy, quality and efficient work methodsAnalytical method validation and GMP working experience is preferredFluent in both German and English , both written and spoken (B2 / C1)Able to work effectively in a team, strong willingness to learn and independent way to workThe selected candidate will be part of a multidisciplinary team and support the development of novel biopharmaceuticals.