Jobs at Evotec

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 Automation & MES Engineer leads the design, implementation, and optimization of MES and process automation in a regulated environment, ensuring compliance and enhancing manufacturing capabilities.

The Senior Scientist will conduct in vitro ADME assays, experimental design, and data analysis while guiding junior scientists and managing multiple projects.

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 Director of Business Development leads sales efforts in the Benelux region by driving new business growth, managing client relationships, and ensuring client satisfaction in Drug Discovery and Pre-Clinical Development services.

The Director of Business Development will drive new business growth in DACH and Southern Europe, managing the full sales cycle and ensuring high client satisfaction while achieving sales targets.

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.

The Scientist will conduct method development assays, support data analysis, and coach colleagues while maintaining laboratory standards and equipment.

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

The QA Associate executes day-to-day QA responsibilities in GMP manufacturing, ensuring compliance with cGMPs, reviewing batch records, and supporting audits while collaborating cross-functionally.

The QA Senior Specialist ensures compliance in cGMP operations, trains junior staff, reviews documents, leads audits, and manages quality compliance issues.

The QA Specialist ensures compliance with cGMP in biopharmaceutical manufacturing by reviewing Batch Records, conducting audits, and collaborating with cross-functional teams. Responsibilities include training staff, investigating manufacturing events, and monitoring product quality.