Jobs at Evotec

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

The Automation CSV Engineer supports validation, compliance, and testing for GMP automation systems, ensuring they remain compliant and operational. Responsibilities include documentation, testing, collaboration across teams, and maintaining regulatory standards.

The Quality Risk Manager ensures compliance with quality systems, manages site risk registers, coordinates risk assessments, and provides guidance on risk mitigation strategies.

Conduct and design in vitro ADME/metabolism assays, analyze and interpret data, troubleshoot and validate assays, mentor junior scientists, maintain lab quality systems, run/maintain robotic systems, and support client-facing project delivery.

Support downstream cGMP manufacturing for clinical-scale continuous processing trains. Serve as MSAT SME on projects, author process documentation, lead investigations and change controls, monitor process performance, provide 24/7 on-call production support, and drive continuous improvement using Operational Excellence and Quality by Design principles.

Support GMP manufacturing lot disposition by compiling lot release documentation, coordinating deliverables, facilitating disposition meetings, reviewing deviations/OOS/change controls, and escalating quality/compliance risks while partnering with QA, Manufacturing, QC, and Facilities.

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.