Principal Automation & MES Engineer Site based, Redmond, WA

Job Title: Principal Automation & MES 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 whats possible. Were on a mission to create a place where curiosity isnt just encouragedits celebrated.

Are you someone who asks questions seeks answers and isnt afraid to go deeper #BeCureious with us and see where your curiosity can take you!

The Role: / your challenge in our journey

Were looking for a passionate and curious Principal Automation & MES Engineer to join our team. If youre excited by new challenges solving complex problems and learning every step of the way you might just be the perfect this role youll have the opportunity to drive impactful projects collaborate with bright minds and explore uncharted territories.

As a Principal Automation & MES Engineer at Just-Evotec youll have the freedom to ask the hard questions think outside the box and find creative solutions that push us forward. Its a role where your curiosity will fuel both your personal growth and the success of the team.

What Youll Do:

The Principal Automation & MES Engineer is responsible for the design implementation optimization and lifecycle management of Manufacturing Execution Systems (MES) process automation systems and digital manufacturing technologies within a regulated manufacturing environment. This role serves as a senior technical leader supporting enterprise manufacturing operations operational excellence initiatives and digital transformation strategies across manufacturing sites.

While MES technologies are a primary area of responsibility this position is broader in scope and includes leadership in automation architecture systems integration process control strategy validation governance and manufacturing systems modernization. The ideal candidate combines deep technical expertise with strong engineering leadership cross-functional collaboration and strategic thinking to deliver scalable and compliant manufacturing solutions.

This role will partner closely with Manufacturing MSAT IT Quality Validation Engineering and external system integrators to drive innovation maintain system reliability and support expansion of advanced manufacturing capabilities.

Key Responsibilities

• 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 and support implementation of Industry 4.0 capabilities including process data integration automation connectivity and advanced manufacturing analytics.

• Provide technical leadership for automation and process control systems including DeltaV SCADA PLC HMI and related manufacturing control platforms.

• Support development and implementation of automation strategies for manufacturing processes utilities and process equipment.

• Lead or support complex troubleshooting root cause investigations deviation investigations and corrective actions related to manufacturing automation and MES systems.

• Evaluate and implement innovative technologies to improve manufacturing flexibility reliability and process performance.

• Lead integration efforts between manufacturing systems and enterprise applications to ensure reliable and compliant data flow across the manufacturing ecosystem.

• Develop and review system architectures functional specifications design documents and interface strategies for manufacturing technologies.

• Provide oversight of external vendors system integrators and contractors supporting manufacturing systems projects.

• Support cybersecurity data integrity disaster recovery and infrastructure reliability initiatives related to manufacturing systems.

• Ensure manufacturing systems remain compliant with GMP FDA GAMP5 and 21 CFR Part 11 requirements.

• Author review and approve validation documentation including URS FRS DS IQ/OQ/PQ protocols risk assessments traceability matrices and test scripts.

• Support regulatory inspections audits and quality investigations related to manufacturing systems and automation platforms.

• Drive adoption of risk-based validation methodologies and continuous improvement of CSV and SDLC practices.

• Lead or contribute to capital projects system implementations upgrades migrations and site expansion initiatives.

• Develop project scopes schedules resource plans and technical execution strategies for manufacturing systems projects.

• Coordinate cross-functional teams and stakeholders to ensure project deliverables timelines budgets and quality expectations are achieved.

• Provide technical and strategic input into long-term manufacturing technology planning and operational roadmaps.

• Identify opportunities to improve manufacturing efficiency data visibility system reliability and process robustness through automation and MES enhancements.

• Drive standardization and harmonization of manufacturing systems across sites and programs where applicable.

• Support development of KPIs system performance metrics and reporting capabilities to enable data-driven decision making.

• Stay current on emerging technologies industry trends and best practices in MES automation and digital manufacturing.

• Serve as a subject matter expert for MES automation validation and manufacturing systems engineering.

• Mentor junior engineers and provide technical coaching across automation and manufacturing systems disciplines.

• Influence engineering standards governance processes and best practices across the organization.

• Lead technical reviews design discussions and strategic engineering initiatives with senior stakeholders.

Position Requirements

• Bachelors or Masters degree in Engineering Computer Science Biotechnology Automation or related technical discipline.

• 10 years of experience in pharmaceutical biotechnology medical device or other regulated manufacturing environments.

• Strong experience with Manufacturing Execution Systems (MES) platforms such as PAS-X Syncade PharmaSuite Opcenter or equivalent.

• Experience with process automation platforms such as DeltaV Siemens Allen-Bradley Wonderware Ignition or related technologies.

• Demonstrated experience supporting validated manufacturing systems within GMP-regulated environments.

• Strong understanding of FDA regulations GAMP5 SDLC methodologies and 21 CFR Part 11 compliance requirements.

• Proven experience leading complex technical projects and cross-functional engineering initiatives.

• Experience with system integration manufacturing data flows and enterprise application connectivity.

• Strong analytical troubleshooting organizational and communication skills.

• Ability to work effectively across global teams manufacturing sites and external partners.

Preferred Qualifications

• Experience supporting global manufacturing operations or Center of Excellence (CoE) initiatives.

• Experience with continuous manufacturing single-use systems or advanced bioprocessing technologies.

• Knowledge of data historians analytics platforms and industrial networking concepts.

• Experience with cloud-connected manufacturing systems and digital transformation initiatives.

• Prior involvement in regulatory inspections and audit support.

• Experience managing or mentoring engineering teams and technical resources.

• PMP Lean Six Sigma or automation/manufacturing certifications are a plus.

Travel & Work Flexibility

• Occasional travel to manufacturing sites and global locations may be required.

• Flexibility in working hours may be necessary to support collaboration across multiple time zones and manufacturing operations.

Why Join Us:

• Growth Opportunities: Were a company that believes in continuous learning and development. Whether its professional courses mentorship or new projects well 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: Were committed to building a diverse and inclusive environment where everyones voice is valued and curiosity is encouraged.

• Innovative Projects: Youll 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 dont just talk about thinking outside the boxwe throw the box away. If youve got ideas we want to hear them.

Are You Still Curious

If youve read this far then chances are youve got a curious mindjust like us. So what are you waiting for Take the leap and apply today. We cant wait to see where your curiosity leads youand 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 $134000 to $154100; Base salary offered may vary depending on individuals 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.