Evotec

Compliance

• Lead deviation investigations and root cause analyses to identify, document, and resolve manufacturing and quality events.
• Demonstrate strong technical problem-solving capabilities and excellent technical writing skills to support compliance documentation and investigations.
• Drive continuous improvements in processes and methods that reinforce cGMP within the department and/or across the site
• Partner with cross-functional stakeholders to identify, develop, and implement effective Corrective and Preventive Actions (CAPAs) that prevent recurrence of deviations and address underlying issues.
• Analyze and trend deviations, CAPAs, and compliance metrics to identify recurring issues, emerging risks, and opportunities for improvement.
• Develop and implement novel approaches to solving non-routine technical and compliance challenges.
• Communicate information effectively through updates, reports, and summaries.
• Support and participate in internal audits, client audits, and regulatory inspections conducted by global health authorities.
• Apply systematic thinking processes and technical knowledge to independently address a broad range of non-routine to moderately complex problems
• Collaborate with operational teams to implement process improvements while maintaining regulatory compliance.
• Support GMP training or knowledge sharing initiatives to foster a culture of quality, compliance, and continuous improvement.
• Provide routine updates on campaign, project, and investigation status, including risks, challenges, and mitigation plans.
• Provide support and/or direction to junior staff when necessary
• Exercise sound judgment and make data-driven decisions within established quality and compliance frameworks.
• Make critical decisions in collaboration with key stakeholders
• Demonstrate accountability for personal, departmental, and organizational initiatives.

Manufacturing Compliance Specialist

QA Automation Engineer

• The Principal Automation & MES Engineer is responsible for the design, implementation, optimization, and lifecycle management of Manufacturing Execution Systems (MES)
• Lead the design, configuration, deployment, and continuous improvement of MES solutions to support manufacturing operations, electronic batch execution, data integrity, and operational efficiency
• Support integration of MES platforms with enterprise and site systems including ERP, LIMS, historians, SCADA/DCS, CMMS, and data analytics platforms
• Define and maintain MES governance, standards, lifecycle management practices, and system roadmaps aligned with business objectives
• Participate in enterprise digital manufacturing initiatives
• Provide technical leadership for automation and process control systems including DeltaV, SCADA, PLC, HMI, and related manufacturing control platforms
• Ensure manufacturing systems remain compliant with GMP, FDA, GAMP5, and 21 CFR Part 11 requirements
• Lead or contribute to capital projects, system implementations, upgrades, migrations, and site expansion initiatives
• Identify opportunities to improve manufacturing efficiency, data visibility, system reliability, and process robustness

Principal Automation, MES Engineer

Analyst

• Support the Order-to-Cash (O2C) process by ensuring accurate data entry, timely processing of transactions, and adherence to established procedures.
• Assist in revenue forecasting activities by preparing reports, gathering data, and coordinating with FP&A and commercial teams.
• Contribute to forecasting process improvements by identifying data or workflow inconsistencies and suggesting potential enhancements.
• Support revenue recognition activities by maintaining accurate records and ensuring transactions comply with relevant accounting policies.
• Help prepare and review revenue-related reports to ensure accuracy, consistency, and compliance with internal controls and standards.

Junior Global Revenue Analyst

Account Manager

• Develop and execute a forward-looking partnership thesis aligned with market evolution and platform priorities
• Design complex, multi-asset and platform-based alliances including risk-share and co-development models
• Structure IP, governance, economics, and milestone frameworks to optimize long-term portfolio value
• Exit or restructure partnerships when strategic value no longer aligns
• Conduct systematic market scanning to identify emerging science, technology inflection points, and capital flows
• Anticipate future innovation clusters and shape participation in these ecosystems
• Build regional and global partnership strategies aligned with Evotec’s long-term growth agenda
• Lead negotiations with C-suite and Board-level stakeholders
• Translate scientific and translational strategy into commercially viable deal structures
• Balance risk, capital exposure, and resource allocation across a diversified partnership portfolio
• Align scientific, legal, finance, and operational functions from concept to contract and into launch
• Establish governance models that enable effective decision-making and execution
• Drive internal alignment across geographies and therapeutic areas
• Articulate strategic rationale and long-term value creation to executive committees and external partners

SVP – Strategic Partnerships

General

• Develop a thorough understanding of European, North American and Asian key funding schemes, and associated application processes
• Expand Evotec's global network of funders proactively and work directly with funding organisations
• Seek, evaluate, and brief senior staff on novel grant opportunities
• Support Evotec researchers actively in preparing competitive applications
• Take a leading role in continuous review and development of grant management processes and procedures
• Work efficiently across teams at the various Evotec sites in Europe, and USA

Senior Grant Management Specialist

Marketing

• Develop and execute integrated marketing campaigns aligned with Evotec’s commercial priorities and growth objectives.
• Design multi-channel programs across digital and physical channels (web, SEO/SEM, email, social media, webinars, conferences, and events) to generate qualified pipeline.
• Support account-based marketing (ABM) initiatives that engage priority pharma and biotech accounts and drive progression from awareness to commercial opportunities.
• Translate Evotec’s scientific capabilities into clear and differentiated value propositions and market narratives.
• Contribute to category narratives that position Evotec within integrated CRO–CDMO models and partnership-based R&D collaborations.
• Oversee the development of high-quality marketing content including whitepapers, case studies, application notes, blogs, videos, and data-driven visuals.
• Define and track marketing performance metrics to measure campaign effectiveness and pipeline contribution.
• Generate insights from campaign performance, market intelligence, and customer engagement data to improve marketing effectiveness.

Marketing Manager

Engineer

• Represents site MSAT on project teams as technical subject matter expert (SME)
• Develops process understanding and expertise
• Authors, reviews and owns process related documentation (technical documents, test protocols, batch records, process descriptions, SOPs, etc)
• Authors, reviews change controls including managing change implementation
• Utilizes technical skills and process knowledge to participate and/or lead investigations related to process/New product implementation
• Collaborates with impacted groups to drive implementation of CAPAs from approval to closure & effectiveness check
• Monitors and reports on process performance data analysis
• Shares 24/7 on call support activities during production
• Applies Operational Excellence principles to lead continuous improvement for downstream process improvements.

Process Engineer II – Downstream

• Lead the generation of key deliverables in a phase appropriate compliance manner as part of global CQV strategy for F&U, Equipment, QC/Analytical, Cleaning and Shipping
• Document a strategy for validations programs including the generation of validation master plans
• Liaise with the equipment, operations, logistics, qc, tech transfer, process development teams and third-party contractors, as applicable, to define and identify and perform cycle development, qualification and validation activities
• Author validation documentation including, but not limited to, risk and gap assessments, cycle development protocols / reports / procedures, qualification/validation protocols and reports, and validation discrepancies.
• Lead validation discrepancy resolution including troubleshooting and root cause analysis
• Support the development of the qualification and validation programs at Just including the transition from paper based to digital validation software to configure globally scalable end to end paperless solutions to manage the validation lifecycle
• Develop and strategize compliant and novel ways to comply with regulatory requirements
• Support inspection readiness activities, Health Authority and Client audits, and support corrective actions based on audit findings
• Lead CQV activities across global expansion sites

Validation Engineer III

• Work with key stakeholders and vendors to evaluate new technologies for implantation into the manufacturing process to increase efficiency and facility throughput.
• Develop design documents (user requirement specifications, software functional specifications) based on platform process requirements and validation commissioning and qualification protocols
• Collaborate with the automation team on design and development of the Distribute Control System (DCS) with the manufacturing suite.
• Support technical evaluations of the facility utility requirements.
• Lead evaluation of single-use technologies and design single-use manifolds and assemblies.
• Work with vendors to develop data and validation packages supporting technologies.
• Facilitate procurement and implementation of approved new technologies.
• Develop business processes, guidelines, SOPs, and training for processing equipment and technologies .
• Lead the development equipment maintenance & life cycle plans.
• Lead non-conformance/deviation investigations and provide process impact evaluations of equipment/technology issues.
• Lead technical exchanges problems and solutions throughout the manufacturing network.
• Participate in internal and external audits/inspections.

Process Engineer III, Global MSAT

Manager

• Schedule and document maintenance related services for manufacturing equipment activities, including facilities and utilities.
• Actively partner and communicate with key internal/external stakeholders to develop a maintenance strategy and definition of facilities maintenance activities within the manufacturing, QC, PD and utilities and facilities areas.
• Serve as a Subject Matter Expert (SME) for facilities and utilities reliability centered maintenance for control systems; including support to predictive maintenance to main electrical distribution systems and life safety systems to ensure full compliance with the good facilities management guidelines and regulations.
• Develop maintenance strategies, plans, SOPs, parts lists, BOMs, and frequency schedules for new and modified equipment.
• Collaborate with safety, quality engineering, and manufacturing teams to perform equipment assessments.
• Review, improve, and update maintenance SOPs, parts lists, BOMs, and ensure CMMS data integrity for existing equipment.
• Analyze CMMS data to identify trends and prioritize areas for improvement.
• Conduct functional equivalency assessments for spare parts.
• Support or lead equipment troubleshooting efforts in collaboration with engineering, manufacturing, and facilities maintenance team.
• Lead and facilitate Root Cause Failure Analysis (RCFA) and Failure Mode and Effects Analysis (FMEA).
• Drive Reliability Centered Maintenance (RCM) improvement initiatives within assigned areas.
• Serve as the Reliability Engineering subject matter expert (SME) during audits.
• Lead the implementation of predictive maintenance technologies to enhance equipment up time.
• Participate in technical reviews for equipment design projects.
• Contribute to Factory Acceptance Testing (FAT) and commissioning of new or modified equipment as needed.
• Identify and lead cost, waste, and energy reduction opportunities.
• Lead carbon footprint reduction initiatives.
• Manage assigned tasks related to change control, Quality CAPAs, and Safety CAPAs.
• Track, maintain, and publish maintenance performance metrics/statistics.
• Perform other duties as assigned.

Senior Facilities Manager, Reliability

Security Engineer

• Design, implement, and maintain security controls and solutions across various technological domains
• Plan, implement, and maintain cybersecurity tools
• Collaborate with security architects and the SOC
• Conduct security assessments, vulnerability scans, and penetration tests
• Support the SOC and participate in incident detection and response activities
• Work with cross-functional teams and IT stakeholders
• Develop and maintain system documentation, technical guidelines, standards, and procedures
• Stay updated on the latest security trends, technologies, and best practices