Our in vitro DMPK team is seeking a motivated scientist with in-depth in vitro ADME expertise.
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:
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