Jobs at Evotec

Perform high- and low-throughput in vitro ADME/Tox assays, maintain mammalian cell lines, prepare compounds and buffers, operate and maintain lab equipment, analyze and document data, support assay execution and trainee mentoring while following quality, safety, and SOP requirements.

Execute warehouse and distribution tasks—goods receipt, storage, provisioning, cycle counts, packing, labeling, and shipping—using ERP/WMS and scanners. Monitor inventory, support compliant clean/safe work, follow SOPs, apply lean methods, and coordinate with labs and couriers.

Laboratory-based role performing metabolite identification and reactive metabolite assays. Conduct routine assays, prepare compounds and buffers, maintain and validate equipment, analyze and interpret data, document results per SOPs, and report errors promptly while meeting tight deadlines.

The Senior Automation Engineer will oversee the AVEVA PI system deployment, integration with process control systems, and ensure data governance in a global manufacturing environment.

Perform and lead in vitro toxicology assay planning, execution, analysis and reporting for discovery and development compounds. Develop and validate high-content, imaging- and MEA-based assays, run high-throughput studies and robotic systems, guide junior scientists, perform quality reviews, and collaborate with project managers to meet client requirements while maintaining quality system adherence.

The Senior Scientist will design and optimize high-throughput protein purification workflows, drive automation efforts, and ensure quality data delivery for drug discovery.

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

Lead design, optimization, and scale-up of protein expression workflows across E. coli, mammalian, and insect systems; develop high-throughput and automated expression platforms; integrate downstream purification and analytics; apply scripting (Python/R) and LIMS for data traceability; manage multiple projects, mentor staff, and communicate results internally and externally to support drug discovery.

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.

Lead global MSAT technology transfer and process validation for late-stage and commercial biologics. Drive site-to-site transfers, develop global templates/protocols (PPQ, PQ, batch records), perform gap/risk analyses and mitigation, analyze process data and annual reviews, support regulatory CMC documentation and inspections, and mentor junior engineers.

The HT-Analytical Senior Scientist plans and conducts analytical assays, provides scientific support, ensures data accuracy, and manages junior team members while driving assay development and compliance with quality standards.