Jobs at Evotec

Supports Benchling and laboratory information systems through user assistance, compliance monitoring, data curation, documentation, training, testing, and troubleshooting. Maintains accurate, synchronized research records across Benchling, Dotmatics, and Limfinity; reviews legacy data, tracks corrective actions, supports cell-line workflows, and coordinates with scientists, technicians, quality, and IT teams. Creates manuals and release notes, delivers onboarding, tests system updates, validates fixes, and reports data-quality issues.

Supports Benchling and related laboratory information systems through user assistance, compliance monitoring, data curation, documentation, training, feature testing, and troubleshooting. Reviews and corrects research records, coordinates cell line workflows, maintains data quality and compliance tracking, and validates fixes across Benchling, Dotmatics, and Limfinity. The role collaborates with scientists, technicians, Cell Core, quality stakeholders, and IT while producing manuals, release notes, reports, and training materials.

Oversee quality management across pharmaceutical research and bioanalytical activities, including GRP, GLP, and GCP compliance. Manage quality documentation, internal audits, sponsor audits, inspections, investigations, deviations, non-conformances, complaints, CAPAs, and quality metrics. Provide training and guidance on data integrity, documentation practices, and risk-based quality principles while collaborating with global stakeholders to promote harmonization and continuous improvement.

Leads high-throughput analytical method development for nonstandard compounds using LC-MS and LC-MS/MS workflows supporting ADME and regulatory DDI studies. Plans and conducts method qualification, documents results, troubleshoots instrumentation, ensures compliance with SOPs and quality policies, evaluates new technologies, and serves as a senior contact for internal and external stakeholders. Coaches and line-manages junior team members while influencing analytical capability development.

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.

Oversee global deployment, architecture, integration, validation, governance, and lifecycle management of AVEVA PI and automation systems supporting cGMP biologics manufacturing. Integrate PI with DeltaV, SCADA, and DCS platforms; develop analytics, reporting, and visualization; support process control, OT infrastructure, SDLC, NPI, MES readiness, audits, CAPAs, and change controls. Provide technical guidance, troubleshooting, documentation, validation protocols, and vendor oversight across manufacturing sites.