Our in vitro DMPK team is seeking a motivated scientist with in-depth in vitro ADME expertise. RESPONSIBILITIES Planning, conducting, evaluating, and reporting of the following in vitro ADME experiments in adequate quality and in compliance with delivery timelines: Protein binding CYP inhibition & induction Whole blood distribution Microsomal and hepatic clearance Drug transporter investigations Review and interpret analytical data and take responsibility for accuracy and compliance. Leading all aspects of studies to ensure data accuracy and report quality Assisting in the preparation of presentations, customer visits and audits Identify issues and provide technical troubleshooting in in vitro ADME experiments Ensure compliance with regulations (e.g. GxP guidelines, radiation protection) in relation to R&D processes, study conduct and drug registration Creation of quality-relevant documents such as SOPs QUALIFICATIONS PhD / post-doc in life sciences (e.g. chemistry, biochemistry, pharmacy) or equivalent In-depth knowledge and hands on experience with in vitro ADME studies i.e. distribution, metabolism, and transporter studies. Profound experience in bioanalytical LC-MS/MS methods Profound knowledge of international regulatory guidelines for in vitro DMPK and drug-drug interaction evaluation from EMA, FDA, ICH in particular Collaborative, self-driven and enthusiastic personality with excellent communication and presentation skills, capable to work both as team player and project driver. Excellent communication in English (written and spoken), advanced knowledge in German WE OFFER Unlimited contract, 30 days holiday per year, flexible working hours (37.5 per week) including a modern workplace Employer-funded pension Comprehensive induction and individual training and development Free parking spaces directly on site and a canteen in-house A dynamic, future-oriented, and employee-oriented company, with room for growth and your own ideas Interdisciplinary, agile teams with flat hierarchies