Job Title: Automation CSV Engineer Location: Redmond, WA Department: Global MSAT About Us: this is who we are At Evotec, we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team, we thrive on challenging the status quo, learning from each other, and pushing the boundaries of what’s possible. We're on a mission to create a place where curiosity isn't just encouraged—it’s celebrated. Are you someone who asks questions, seeks answers, and isn't afraid to go deeper? #BeCureious with us and see where your curiosity can take you! The Role: / your challenge, …in our journey The Automation CSV Engineer is responsible for supporting validation, compliance, testing, and technical documentation activities for GMP automation systems within a regulated manufacturing environment. This role partners closely with Automation, Quality Assurance (QA), IT CSV, Manufacturing, and Engineering teams to help ensure automation systems remain compliant, reliable, and maintained in a validated state throughout the system lifecycle. What You’ll Do: Position Summary The Automation CSV Engineer provides validation and compliance support for automation and computerized systems used in GMP manufacturing operations. The position is responsible for developing validation strategies, preparing and executing lifecycle documentation, assessing automation changes, and helping maintain systems in a controlled and validated state. This role works across Automation, Quality Assurance, IT, Manufacturing, Engineering, Validation, and external service providers. The engineer will apply technical knowledge of manufacturing control systems and risk-based validation practices to support system implementations, upgrades, modifications, periodic reviews, and ongoing operations. Successful candidates will have practical experience with platforms such as Emerson DeltaV, OSIsoft PI or AVEVA PI System, SCADA, PLC-based controls, batch systems, and associated interfaces. The role requires strong technical writing, disciplined documentation practices, and the ability to translate technical system behavior into clear and defensible validation evidence. Key Responsibilities Automation System Validation Develop and support lifecycle validation strategies for GMP automation systems, including DeltaV, process historians, SCADA platforms, PLC controls, batch applications, and supporting infrastructure. Define the appropriate validation deliverables based on intended use, system complexity, configuration, product or process impact, and risk. Support new system implementations, expansions, upgrades, migrations, security updates, patches, and decommissioning activities. Evaluate automation changes for validation impact and determine the testing, documentation, and approval requirements needed before release. Help ensure validated systems remain fit for intended use throughout their operational lifecycle. Support the transition of new or modified systems from project delivery into site operations and ongoing system ownership. Lifecycle Documentation Author, review, revise, and maintain validation and engineering documents, which may include: Validation plans and system validation plansUser requirements and functional requirementsFunctional and configuration specificationsSystem and data flow descriptionsRisk assessmentsRequirements traceability matricesCommissioning and qualification protocolsIQ, OQ, and PQ protocolsAutomation functional test scriptsValidation discrepancy and deviation recordsValidation summary reportsStandard operating procedures and work instructions Confirm that requirements are clear, testable, traceable, and appropriate for the system’s intended use. Ensure executed documentation is complete, legible, attributable, technically accurate, and consistent with site procedures. Route documents through applicable document management and electronic quality management systems. Work with reviewers and approvers to resolve comments efficiently while preserving technical and compliance integrity. Testing and Qualification Plan, coordinate, witness, or execute FAT, SAT, commissioning, qualification, regression, and functional testing for automation systems. Verify control system functions such as sequences, phases, recipes, interlocks, alarms, permissives, calculations, interfaces, security roles, electronic records, and exception handling when applicable. Record objective evidence demonstrating that systems and configured functions meet approved requirements. Identify and document test exceptions, discrepancies, and unexpected results in accordance with established procedures. Support troubleshooting and retesting activities with automation engineers, system integrators, vendors, and process subject matter experts. Assist in determining the impact of test failures and confirm that corrective actions are completed before final acceptance. Coordinate validation execution with project schedules, manufacturing availability, shutdown periods, and operational readiness milestones. Risk-Based Assurance and Data Integrity Apply risk-based validation principles consistent with applicable regulations, company procedures, and recognized industry practices. Facilitate or contribute to system risk assessments, functional risk assessments, data integrity assessments, and validation impact assessments. Use critical thinking to scale testing rigor and documentation depth according to intended use, patient or product risk, process criticality, and system complexity. Evaluate GMP data flows, interfaces, calculations, records, and reporting functions for completeness and integrity. Support assessments of audit trails, electronic signatures, access controls, account management, backup and recovery, time synchronization, and record retention where applicable. Help ensure automation records support ALCOA+ data integrity principles. Participate in periodic reviews and other activities used to confirm the continued validated state of GMP systems. Change Control and Quality System Support Provide automation and CSV input to change controls, deviations, CAPAs, investigations, and system lifecycle records. Assess proposed configuration, hardware, software, infrastructure, recipe, interface, and security changes for GMP and validation impact. Support root cause investigations for automation-related events and documentation discrepancies. Define or review corrective actions, remediation testing, and effectiveness checks when required. Monitor validation commitments and communicate risks that could affect project delivery, manufacturing readiness, or system release. Contribute to inspection readiness, internal audits, client audits, and regulatory inspection support. Retrieve and explain validation evidence to auditors, inspectors, and quality representatives as needed. Cross-Functional Delivery Partner with Automation, QA, IT, Engineering, Manufacturing, Validation, and system owners to align technical execution with quality requirements. Gather and clarify system requirements with process owners, operators, engineers, and technical SMEs. Participate in design reviews, project meetings, change review boards, risk workshops, deviation investigations, and release readiness discussions. Review vendor and system integrator documentation for technical adequacy, traceability, and suitability for use as validation evidence. Coordinate vendor testing and ensure supplier documentation is appropriately assessed before acceptance. Communicate validation status, open issues, decisions, and schedule risks to project and functional stakeholders. Promote consistent validation practices across automation projects and operational support activities. Operational and Lifecycle Support Review automation configurations and supporting infrastructure for compliance and validation impact. Support user access reviews, account recertification, backup verification, restore testing, audit trail review, and disaster recovery activities as assigned. Assist with system health assessments, periodic reviews, lifecycle planning, and obsolescence evaluations. Work with Automation and IT/OT teams to support system availability, cybersecurity controls, operational continuity, and controlled maintenance. Develop or improve templates, test methods, procedures, and tools that increase validation efficiency without reducing assurance. Maintain awareness of evolving regulatory expectations, automation technologies, and industry practices relevant to computerized systems. Required Qualifications Bachelor’s degree in Engineering, Computer Science, Information Systems, Biotechnology, Life Sciences, or a related technical discipline, or an equivalent combination of education and relevant experience. At least five years of experience in automation validation, computer system validation, commissioning and qualification, automation engineering, or computerized system quality within a regulated environment. Working experience with one or more industrial automation technologies, such as: Emerson DeltaVAVEVA PI System or OSIsoft PISCADA platformsPLC and HMI systemsBatch control systemsManufacturing data collection or reporting applications Experience creating and executing validation or qualification deliverables, including FAT, SAT, IQ, OQ, PQ, regression testing, or automation functional testing. Demonstrated ability to author clear, technically accurate validation documentation. Knowledge of GMP system lifecycle controls and applicable requirements or guidance, including: 21 CFR Part 11EU GMP Annex 11GAMP 5Data integrity principlesRisk-based computerized system assurance practices Experience working within formal quality systems, including change control, deviations, CAPAs, and risk management. Understanding of automation system architecture, interfaces, configuration management, and operational support. Ability to manage multiple deliverables and priorities while maintaining documentation quality and schedule awareness. Strong communication skills and the ability to work effectively with both technical and nontechnical stakeholders. Preferred Qualifications Direct experience validating or supporting Emerson DeltaV in a GMP manufacturing environment. Experience with DeltaV batch configuration, phases, recipes, modules, alarms, interlocks, security, or system interfaces. Experience in pharmaceutical, biotechnology, biologics, cell therapy, gene therapy, or medical device manufacturing. Familiarity with MES, electronic batch records, process historians, laboratory systems, building automation systems, or manufacturing data platforms. Experience with system integration involving OPC, databases, middleware, reporting tools, or industrial network infrastructure. Familiarity with electronic document management systems, eQMS platforms, and electronic validation tools. Experience supporting GMP system upgrades, migrations, disaster recovery testing, or cybersecurity remediation. Knowledge of software development lifecycle and configuration management practices. Experience reviewing vendor documentation and leveraging supplier testing or engineering records as validation evidence. Previous participation in regulatory inspections, client audits, quality audits, or remediation programs. Experience working with automation system integrators, equipment vendors, validation service providers, or managed service partners. Travel and Work Flexibility Occasional travel to manufacturing, vendor, or project locations may be required. The position may require schedule flexibility during system cutovers, testing campaigns, manufacturing shutdowns, qualification execution, or critical issue resolution. Work may occasionally be performed in manufacturing, laboratory, utility, or controlled production areas in accordance with site safety and gowning requirements. Why Join Us: Growth Opportunities: We’re a company that believes in continuous learning and development. Whether it’s professional courses, mentorship, or new projects, we’ll help you grow. Flexible Work Environment: We offer flexible work options to help you balance your professional and personal life. Site based role. Inclusive Culture: We’re committed to building a diverse and inclusive environment where everyone’s voice is valued, and curiosity is encouraged. Innovative Projects: You’ll have the chance to work on groundbreaking initiatives and cutting-edge technology in an atmosphere where your curiosity is the key to success. A Place for Big Ideas: We don’t just talk about thinking outside the box—we throw the box away. If you’ve got ideas, we want to hear them. Are You Still Curious? If you’ve read this far, then chances are you’ve got a curious mind—just like us. So, what are you waiting for? Take the leap and apply today. We can’t wait to see where your curiosity leads you—and how it will shape the future of Evotec. Let your curiosity guide your career—#BeCurious and explore the endless possibilities at Evotec! The base pay range for this position at commencement of employment is expected to be $115,000 to $126,500; Base salary offered may vary depending on individual’s skills, experience and competitive market value. Additional total rewards include discretionary annual bonus, comprehensive benefits to include Medical, Dental and Vision, short-term and long-term disability, company paid basic life insurance, 401k company match, flexible work, generous paid time off and paid holiday, wellness and transportation benefits. Evotec (US) Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, gender, age, disability, genetic information, gender expression, gender identity, national origin, religion, sexual orientation, or veteran status. Established in 1999, Cyprotex has over 150 staff based at its sites in the UK (Alderley Park in Cheshire) and in the USA (Watertown, MA). We operate as a contract research organisation and we have over 1700 customers worldwide within industries such as the pharmaceutical, cosmetics and personal care and the chemical and agrichemical markets. Outstanding customer service excellence and quality are key focuses of the business. In addition to our customer projects, we invest heavily in Research and Development of new techniques – many of these projects are exploring new in vitro or in silico methods to understand how chemicals or new pharmaceuticals may behave in humans in terms of their safety or efficacious effects. Cyprotex is a growing and successful business and we are constantly recruiting for motivated and hardworking staff who thrive within a dynamic and vibrant organisation. We are committed to providing an environment where employees can learn and develop their skills and are recognised and rewarded for the contribution they make to the Company. Much of our work is performed in multi-disciplinary project teams that enables exchange of ideas and knowledge, enabling people to develop and take on additional responsibility either within the team or across teams in the business. Please click on the link below to access and review our Privacy Information for Applicants: Privacy Information for Applicants

Automation CSV Engineer - Site Based, Redmond, WA.

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