Automation CSV Engineer - Site Based, Redmond, WA

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. The ideal candidate will have experience supporting automation validation and Computer System Validation (CSV) activities for manufacturing systems such as DeltaV, PI, SCADA, PLC, and related automation platforms. This position requires strong technical writing skills, attention to detail, and the ability to collaborate effe [... source excerpt omitted ...] tion, ITCSV, Engineering, and Manufacturing teams to support alignment of validation and compliance activities. Collaborate with system owners and technical SMEs to gather system requirements and support risk assessments for automation systems. Participate in project meetings, change control reviews, deviation investigations, and quality discussions related to automation systems. Support vendor and integrator coordination activities as needed for system implementations and upgrades. Risk-Based Validation & Quality Systems Support risk-based validation approaches aligned with FDA CSA principles, GAMP 5 guidance, and Data Integrity expectations. Assist in execution of Quality Ris [... source excerpt omitted ...] ability, compliance, and operational continuity. Maintain awareness of current regulatory guidance and industry best practices related to CSV and automation validation. Position Requirements Bachelor’s degree in Engineering, Computer Science, Biotechnology, Information Systems, or related technical discipline preferred. Minimum of 5 years of experience supporting GMP automation systems, computer system validation (CSV), automation testing, or technical writing activities within regulated industries. Hands-on experience with automation platforms such as DeltaV, PI, SCADA, PLC, or related manufacturing systems. Experience executing validation and qualification activities includin