Jobs at Evotec

Oversee global deployment, architecture, integration, validation, governance, and lifecycle management of AVEVA PI and automation systems supporting cGMP biologics manufacturing. Integrate PI with DeltaV, SCADA, and DCS platforms; develop analytics, reporting, and visualization; support process control, OT infrastructure, SDLC, NPI, MES readiness, audits, CAPAs, and change controls. Provide technical guidance, troubleshooting, documentation, validation protocols, and vendor oversight across manufacturing sites.

Conduct routine high- and low-throughput in vitro ADME assays, process experimental data, maintain mammalian cell cultures and laboratory equipment, support assay validation and troubleshooting, manage consumables, follow safety and quality procedures, and collaborate with laboratory supervisors and senior research scientists.

Supports in vitro toxicology screening and assay development for drug discovery. Performs high-content imaging, mitochondrial toxicity assays, compound and buffer preparation, robotic system operation, equipment calibration, and data analysis. Ensures work meets timelines, quality standards, safety regulations, and relevant toxicology guidelines while contributing to research, commercial projects, and continuous technical development.

Conduct routine toxicology and cell-based assays using manual and automated laboratory systems. Process, analyze, and interpret data; troubleshoot assays and instrumentation; support assay development, validation, and process improvements. Maintain high standards for data integrity, quality control, documentation, and laboratory safety. Coach associate scientists and collaborate with senior scientists and information systems teams in a high-throughput laboratory environment.

The Principal Scientist will manage and conduct ADME assays, lead projects, mentor staff, and drive scientific innovation while ensuring high standards and team collaboration.

Plan, perform, analyze, and report in vitro toxicology and imaging/MEA assays for discovery and development compounds. Develop and validate assays, run high‑throughput studies and robotic systems, mentor junior scientists, perform quality review, and collaborate with project managers to meet client requirements.