Jobs at Evotec

Support execution and validation of routine and bespoke in vitro ADME/Tox screening assays, maintain consumables and equipment, follow safety and quality procedures, document results, assist troubleshooting, and mentor trainees as needed.

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 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.

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.

Execute day-to-day QA activities for GMP manufacturing and maintain/enhance Quality Management Systems. Review and assess eQMS events (Deviations, CAPA, Change Control, etc.), support audits and inspections, deliver QMS training, monitor QMS effectiveness via metrics and trending, and collaborate with Manufacturing, Quality, and Facilities to ensure cGMP compliance and continuous improvement.

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.

Perform routine high- and low-throughput in vitro toxicology screens, process data to quality standards, assist senior scientists with validation and troubleshooting, maintain consumables and lab equipment, follow safety and QC procedures, and support scientific strategy within the team.

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.

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.