Evotec

Learning and Development

• Support our Learning, Leadership, and Talent processes through platforms, tools, and AI solutions.
• Manage and improve EVOacademy (LMS) for user experience and engagement.
• Support EVOconnect / EVOtalks (Workday) for performance and talent processes.
• Work closely with the HRIS team to implement changes and extract data and insights.
• Upload, curate, and maintain digital learning content.
• Support the design and rollout of learning journeys and initiatives.
• Create learning materials and videos using digital and AI tools.
• Manage operational topics such as purchase orders, licenses, and invoicing.
• Use AI tools to improve content creation and team productivity.
• Support the communication of learning initiatives and campaigns.
• Track and report on learning and participation data.

Senior Global Learning Specialist

Director

• Develop JEB’s long-term facility and capacity planning in line with corporate growth strategy
• Provide significant input on yearly capital equipment spend.
• Work with finance to develop ROI cases as needed
• Own and Eexecute various capital projects. This includes creation of a business case, feasibility, design and construction as applicable
• Provide ongoing oversight for contractors, contingent workers and/or workforce needed to execute the various capital projects
• Direct multiple functional teams including capital projects, facilities engineering, and validation with a matrixed organization
• Lead the capital projects review board to ensure appropriate governance and execution per JEB strategy and represent facilities in various corporate planning and strategy discussions; serve as key interface between the capital project and senior leadership
• Partner with the Finance team to plan and manage cash spend and commitments for the various capital projects; own capital project budgets as appropriate
• Provide plant utilities commissioning, qualification, and validation, including risk assessments, user requirement specifications, design qualification, installation qualification, operational qualification, performance qualification, and validation summary reports

Senior Director, Capital Projects

Engineer

• Execute FUSE commissioning and validation activities for early stage clinical manufacturing, late-stage molecule/ commercial manufacturing and/or PPQ campaign support.
• Generate and review technical documentation including validation lifecycle documents, validation protocols and associated reports related to the equipment validation lifecycle.
• In collaboration with cross functional teams, develop Validation Master Plans, provide process knowledge to support the validation execution and risk assessments.
• Lead the development and implementation of templates and validation workflows.
• Support the generation of governance policies and related SOPs for commissioning of FUSE.
• Support validation deviation resolution including troubleshooting and root cause analysis
• Support the periodic review of qualified/validated FUSE across JUST WA sites.
• Support inspection readiness activities, Health Authority and Client audits, and support corrective actions based on audit findings

Validation Engineer II

Project Manager

• In partnership with internal and client/partner technical leaders and as part of the technical team, provide project planning, execution, monitoring and reporting leadership on complex project teams and portfolio programs
• Manage a team of project managers providing project management support to clients and internal project teams
• Lead escalation and decision-making processes within project teams
• Meeting facilitation: facilitate leadership meetings, joint steering committee meetings, on site client meetings
• Risk management: Identify project issues and facilitate resolution, conduct risk management and contingency planning including facilitation of risk assessments
• Development and sponsor of best practices and business processes initiatives: Sponsor teams in the establishment of project management best practices and tools as well as business processes to establish efficiencies to project management organization
• Provide project management leadership and expertise within CMC technical teams

Associate Director, Project Management

• Project Lead for technology transfer of a Late-Stage molecule/ commercial manufacturing and/or PPQ campaign support
• Lead site to site Tech Transfer activities
• Ensure gap analysis/risks assessments are performed and mitigation plans are in place
• Support development, review and approval of technical documentation
• Lead the development and implementation templates for Process Validations
• Analyze process data including annual periodic reviews across the network
• Develop Process transfer document and or Process Control strategy

Principal Process Engineer

• Perform daily project management activities: meeting planning, setting agendas, documenting meeting minutes, tracking and follow up of action items and decisions, document management, ensuring overall team organization
• Timeline management: assist Project Managers and/or Project Team leads with timeline updates and communication to appropriate stakeholders.
• Team support: work closely with Project Managers and/or Project Team Leads to keep project teams on track.
• Assist with development and testing of best practices within the Project Management Organization: software, organizational tools, document management.
• Provide project management support for small to medium scope projects such as process development studies, feasibility studies, resupplies of manufacturing runs, and Phase I clinical process development and manufacturing programs
• Assist Project Managers on large scope projects such as biosimilar development and commercial process development

Associate Project Manager

Systems Engineer

• Design, configure, and maintain enterprise server environments (Windows, Linux, VMware) supporting laboratory and production systems
• Implement robust monitoring, patching, and performance optimization to meet compliance and uptime requirements
• Lead initiatives to improve system availability and disaster recovery for GMP and GxP environments
• Automate system provisioning and configuration using modern tools and scripting
• Deploy and manage hybrid cloud architectures (Azure) for secure data storage and analysis
• Support cloud migration projects for bioinformatics and data-intensive applications
• Ensure compliance with data integrity and security standards in cloud environments
• Apply security best practices aligned with FDA, EMA, and other regulatory requirements
• Conduct system audits and implement remediation plans for compliance gaps
• Collaborate with Quality Assurance to maintain validated systems and documentation
• Lead technical projects involving system upgrades, migrations, and integrations for laboratory and manufacturing systems
• Partner with scientists, automation engineers, and IT teams to deliver solutions that enable research and production workflows
• Provide mentorship and guidance to junior engineers and administrators
• Maintain detailed documentation of system configurations, validation protocols, and SOPs
• Generate reports on system performance, capacity planning, and compliance status

Senior IT Systems Engineer

• Perform daily project management activities: meeting planning, setting agendas, documenting meeting minutes, tracking and follow up of action items and decisions, document management, ensuring overall team organization
• Timeline management: assist Project Managers and/or Project Team leads with timeline updates and communication to appropriate stakeholders
• Team support: work closely with Project Managers and/or Project Team Leads to keep project teams on track
• Assist with development and testing of best practices within the Project Management Organization: software, organizational tools, document management
• Provide project management support for small to medium scope projects such as process development studies, feasibility studies, resupplies of manufacturing runs, and Phase I clinical process development and manufacturing programs
• Assist Project Managers on large scope projects such as biosimilar development and commercial process development

QA Engineer

• Lead the QA Disposition group to ensure compliant and efficient disposition of materials and products
• Perform QA disposition of Cell Banks and DS batches manufactured at Just‑Evotec Biologics
• Perform QA disposition of Cell Banks and DP batches manufactured at contracted CMOs
• Execute raw material disposition to support manufacturing schedules and supply continuity
• Manage QA communication and disposition workflows with CDMO client partners
• Oversee DS/DP shipments to CMOs for fill/finish operations
• Support shipment of DS/DP vials for labeling, stability studies, or other testing needs
• Support internal and client audits of the Quality Management System
• Implement and maintain process performance and product quality monitoring programs
• Guide team members and cross-functional partners through the development and maturation of Quality Assurance programs
• Implement phase-appropriate quality programs that balance scientific flexibility with compliance expectations
• Identify, escalate, and communicate significant quality, compliance, supply, or safety risks to senior leadership
• Identify and escalate compliance risks within the disposition function
• Participate in the strategic development and continuous improvement of Quality Systems
• Compile, analyze, and report team KPIs; lead process improvement initiatives within the disposition area

Senior Manager, QA Disposition

Account Manager

• Develop and execute comprehensive multi-year account strategies aligned with corporate priorities
• Own and evolve account plans for top current and future high-value customers
• Drive revenue growth, retention, satisfaction, and expansion within assigned accounts
• Identify, shape, and close new opportunities within existing accounts
• Proactively develop entry strategies for prospective key customers within the territory
• Build and maintain executive-level relationships, including scientific C-level stakeholders
• Lead Joint Steering Committees and Quarterly Joint Business Reviews
• Define operational success metrics per account and track value realization
• Manage renewal and expansion motions based on performance and strategic alignment
• Shape pipeline opportunities within accounts including upsell, cross-sell, new site, and therapeutic area expansion
• Conduct whitespace analysis and semiannual account tiering reviews
• Balance growth ambition with delivery feasibility and margin discipline
• Lead matrix coordination across R&D, Operations, Legal, Finance, and other enabling functions from opportunity through delivery
• Ensure seamless execution and high customer satisfaction
• Monitor performance against plans and drive corrective actions where required
• Apply disciplined qualification and early-stage filtering of non-promising opportunities

SVP, Key Account Management

Business Development Rep

• Develop and implement a regional sales strategy aligned with global commercial goals
• Assess and refine sales territories and account assignments across the team to maximize efficiency and growth potential
• Build and maintain strong, executive-level relationships with key clients in the region
• Accelerate top-line growth by being accountable for achievement of regional sales target
• Monitor team KPIs and report performance to executive leadership
• Partner with other sales leaders, marketing, commercial strategy and commercial operations to ensure aligned growth strategies
• Represent Evotec at industry events, trade shows, and key client meetings
• Hire, mentor, train, and motivate sales teams to achieve sales and customer satisfaction targets

VP Business Development, Discovery

• Build and execute a comprehensive KAM strategy aligned with corporate vision and growth objectives
• Own 12 to 18 month account plans for top high-value customers including goals, executive mapping, co-innovation roadmaps, risk mitigation plans, and success metrics
• Drive long-term value creation, retention, satisfaction, and share-of-wallet growth
• Assume full responsibility for identifying and closing new opportunities within assigned accounts and achieving agreed sales targets
• Cultivate and expand executive-level relationships within assigned accounts, including new customer development
• Lead Joint Steering Committees and Quarterly Joint Business Reviews with customer executives
• Define operational plans and success metrics per account
• Track value realization, renewal opportunities, and expansion pathways
• Shape account-level pipelines including upsell, cross-sell, new site entry, and therapeutic area expansion
• Develop proactive entry strategies for prospective key customers in the territory
• Monitor industry trends and competitor activity to inform account positioning
• Coordinate R&D, Operations, Legal, and Finance stakeholders from opportunity identification through delivery
• Ensure seamless execution and high customer satisfaction in a matrix environment
• Monitor performance against plan and drive corrective actions where required
• Maintain clear account governance and structured reporting artifacts

VP, Key Account Management

• Lead stakeholders to implement the NPI process at J.POD Redmond and Seattle to support the start and rapid scale-up of commercial GMP manufacturing activities
• Partner with Product and Process Design to coordinate successful efficient scale-up and transfer operations and to ensure the successful integration of process knowledge into manufacturing operations
• Partner with supply chain to support Bill of Material development and demand planning for new products
• Partner with Engineering and Digital disciplines to conduct facility fit assessments and plans to support system updates needed for new product introduction
• Partner with Manufacturing to develop high-quality batch records, robust processes and innovative technology solutions for new product introduction
• Partner with Quality, Validation and Global MSAT to develop and implement process validation and comparability study activities leading to successful product registration
• Utilize the team’s technical skills and process knowledge to participate and/or lead investigations related to NPI activities
• Collaborate with impacted groups to develop and execute effective CAPA
• Apply Operational Excellence principles to lead continuous improvement in NPI activities

Process Engineer III, NPI, Site Based

Vice President

• Define, lead and ensure execution of the multi-year JEB IT & Digital roadmap, aligned with Evotec’s global IT strategy and future IT TOM, from concept through deployment and steady-state operations.
• Act as the senior, hands-on IT partner to JEB Process and Product Design, Manufacturing, and Quality, translating operational needs into scalable, compliant technology solutions.
• Remain personally engaged and accountable in critical design, implementation, validation, and go-live activities, especially for GMP-impacting systems.
• Ensure 24/7 availability, performance, security, and resilience of IT services supporting JEB operations, including triage and problem solving with global leaders for high-impact incidents.
• Own IT systems supporting regulated operations, including SCADA, MES/eBR, ERP, historians, laboratory, and development systems.
• Ensure compliance with cGMP, FDA regulations (including 21 CFR Part 11), and Evotec IT & Data governance, security, and validation standards.
• Establish and maintain robust CSV and data integrity practices, including validation strategy, risk assessments, and inspection readiness.
• Provide IT accountability for regulatory inspections, audits, and remediation activities related to IT systems.
• Actively shape and execute the integration of JEB IT into Evotec’s future IT Target Operating Model, ensuring continuity of operations and compliance throughout the transition.
• Define clear service boundaries, ownership models, escalation paths, and accountability between global IT & Data teams and JEB operations.
• Ensure operational requirements such as time-zone coverage, extended support, and manufacturing uptime are built into global service models.
• Contribute directly to Evotec’s IT & Data transformation initiatives, including prioritization of platform standardization, consolidation, and process harmonization.
• Drive digitalization, automation, and data-driven optimization across Process and Product Design and Manufacturing, with measurable business impact.
• Ensure JEB-specific solutions align with Evotec’s long-term architecture, data strategy, and cybersecurity principles without compromising GMP needs.
• Own and manage JEB-related IT spend including operating and capital budget inclusive of ROI for new programs/software, ensuring value delivery within Evotec’s financial and governance framework.
• Select, negotiate, manage, and actively engage vendors and service partners, ensuring delivery quality, compliance, and operational performance.
• Lead, influence, and coordinate JEB-focused IT capabilities delivered through global IT & Data teams and shared services.
• Drive change management and user adoption, ensuring new systems are operationally embedded, not just implemented.

Vice President, IT – Digitalization

• Achieve a defined yearly sales goal for your region by executing mutually beneficial and profitable business collaborations and partnerships
• Represent Just-Evotec in discussions and work collaboratively with current and potential partners
• Identify solutions when needed to reach agreement on key deal terms
• Lead business development engagements and lead meetings in industry conferences and marketing events
• Manage and coordinate cross-functional team through evaluation of opportunities and interactions with potential partners
• Identify, communicate and manage risks and opportunities with new and existing partnerships and strategic alliances to internal stakeholders across BD, finance and manufacturing leadership
• Contribute to all aspects of business development and strategy.