SeniorExpert-AnalyticalOperations(m/f/d)

**Job Description Summary** Location: Schaftenau, Austria #LI-Hybrid As a Senior Expert you will be part of a team developing new Biologic drugs. Analytical Operations is the team releasing the product for clinical trial and investigating the stability behavior of the drugs. Furthermore, we are validating the methods used for release and will be also responsible for transferring the methods to our commercial organization or external partners. The role will be a mix of overseeing development and authoring/completing documentation. As such, you should be comfortable working in a hybrid environment both in and out of the lab delivery of GMP products. All roles operate with a Future-Ready/Digital First mindset: leveraging data, digital tools, and emerging technologies to improve decision making, accelerate development, and maintain compliance, blending new technologies advancement to core-TRD capabilities. Associates are expected to build digital fluency, innovate responsibly, learn continuously, and collaborate across functions. **Job Description** **Key responsibilities:** * Independently managing key tasks for projects (e.g. release, stability studies, validation, and transfer activities). * Writing protocols, scientific reports, lab procedures and providing ready-to-submit documents intended for submissions (e.g. release or stability documents, transfer reports). * Approving GMP documents and test records as well as investigating quality events within the project (e.g. deviations, changes, out-of-specifications events). * Supporting the lab team in case of troubleshooting existing methods, processes, or solving problems of higher complexity within projects. **Essential Requirements:** * Master’s degree in biotechnology, biochemical engineering, biology, chemistry, biochemistry or similar with at least 4 years strong relevant industry experience or PhD in relevant field or equivalent and 2+ years of work experience within the pharmaceutical industry. * Proficiency in