Jobs at Evotec

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

The Process Engineer III will support downstream tech transfer and manufacturing processes, focusing on late-stage and commercial biologics, documentation creation, and regulatory compliance.

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.

The Senior Scientist Bioassay will conduct QC testing, ensure compliance with GMP, support method development, and mentor junior staff.

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.

Lead design and execution of membrane protein production and characterization across multiple discovery projects. Oversee experiment design, data analysis, quality control, and client deliverables. Optimize expression and purification workflows, support structural and biophysical sample preparation, implement scientific services, mentor colleagues, and represent Evotec in scientific fora and publications.

The Process Engineer II will design and develop new equipment, evaluate technologies, assist with project integration, and support regulatory submissions in a biopharmaceutical environment.

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.

Serve as strategic HR partner advising senior leaders on HR strategy, policies, org design, performance management, employee relations, talent acquisition, and HR programs. Lead annual HR cycles, analyze HR metrics to drive improvements, coach managers, and support organizational change from design through implementation.

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 Senior Scientist will design and optimize high-throughput protein purification workflows, drive automation efforts, and ensure quality data delivery for 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 Principal Process Engineer leads technology transfer and validation for clinical and commercial biologics manufacturing, ensuring compliance and process optimization.

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

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.

The HT-Analytical Scientist will conduct analytical assays, ensure quality and compliance, manage projects, support team training, and enhance processes.

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.