RESPONSIBILITES Manage bioanalytical projects in the role of Principal Investigator or Responsi-ble Bioanalyst according to GLP or GCP regulations Supervise the development, validation and application of LC-MS bioanalytical methods for quantification for small molecule drugs, biologics and biomarkers Discuss analytical results internally and with clients and take ownership of the quality and integrity of the reported data. Author, edit, and review bioanalytical protocols and reports. Communicate relevant project details to laboratory operations in a proactive manner to ensure smooth business operations Discuss new project opportunities and consult clients to develop optimal project designs in association with business development Represent bioanalytical projects during client audits and health authority in-spections in association with Quality Assurance Contribute to creation of clinical laboratory manuals Review service estimates in knowledge of clinical study designs and translate those into adequate bioanalytical protocols QUALIFICATIONS Master or PhD in analytical chemistry or equivalent qualification with a proven track in LC-MS based bioanalysis Distinct project management, problem-solving and analytical skills Experience in regulated quality management systems such as GLP/GCP Excellent communication skills in English and German language Strong personal commitment and high sense of urgency in a quickly changing environment High personal initiative and team spirit WE OFFER Limited employment contract with the option to extend 30 days holiday per year, flexible working hours (37.5 per week) including a modern workplace After the training time option for mobile work 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