Principal Automation/Process Control Engineer – DeltaV Specialist - Redmond, WA

Job Title: Principal Automation/Process Control Engineer DeltaV Specialist (GxP Biologics Manufacturing) - Global MSAT

Location: Redmond WA

Department: Global MSAT

Reports To: Director Automation

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/Process Control 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/Process Control Engineer at 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.

Are you a passionate Automation Engineer with deep expertise in Emerson DeltaV and a drive to revolutionize biologics manufacturing Just-Evotec Biologics is seeking a dynamic Principal Automation/Process Control Engineer to join our Global Manufacturing Sciences and Technology (GMSAT) team in Redmond WA. This is your chance to lead cutting-edge automation initiatives enhance our innovative continuous manufacturing platform and improve global access to life-changing biotherapeutics in a GxP-regulated environment.

As a key member of our automation team youll spearhead the design implementation and optimization of DeltaV-based process control systems (SCADA and DCS) for our state-of-the-art cGMP biologics manufacturing facilities. Youll collaborate globally to ensure standardization across our network tackle complex technical challenges and drive operational excellence in a highly regulated environment. If youre a self-motivated problem-solver with a proven track record in bioprocessing automation GAMP5 validation and FDA compliance we want you to help shape the future of biomanufacturing!

What Youll Do:

• Lead Automation Innovation: Design and implement advanced DeltaV process control schemes to enhance the continuous manufacturing platform including batch tracking process control limits predictive control algorithms and real-time data integration.

• Maintain Global Standards: Oversee the global validated DeltaV library establish governance and manage change control to ensure consistency across Just-Evotecs manufacturing network.

• Drive Strategic Initiatives: Contribute to the global Software Development Life Cycle (SDLC) and roadmap for DeltaV aligning automation strategies with business objectives.

• Collaborate Globally: Partner with Site MSAT Automation teams process engineers data scientists quality assurance and validation teams to support global and site-specific goals.

• Ensure GxP Compliance: Develop and execute detailed specifications IQ/OQ/PQ protocols SOPs and training materials in compliance with FDA 21 CFR Part 11 and GAMP5 guidelines.

• Troubleshoot and Optimize: Lead technical root cause analyses incident investigations and troubleshooting for process control and automation infrastructure issues.

• Support Manufacturing Operations: Provide hands-on technical expertise to manufacturing sites for DeltaV systems automation infrastructure and process optimization.

• Manage Projects: Oversee Process Control System (PCS) implementation projects with third-party suppliers/integrators ensuring timely and successful delivery.

• Continuous Improvement: Drive operational enhancements by integrating automation with single-use technologies predictive analytics and Industry 4.0 principles.

Who You Are:

Education & Experience:

• Bachelors or Masters degree in Engineering Computer Science or related field with 10 years of relevant experience; OR

• Associates degree in a science-related field with 13 years of relevant experience

• 5 years in pharmaceutical biotech or life sciences industries with a focus on GxP-regulated environments.

Technical Expertise:

• Advanced proficiency in Emerson DeltaV (SCADA/DCS) for bioprocessing including coding configuration and system integration.

• Strong background in designing installing programming and validating automated control systems.

• Familiarity with other automation platforms such as Siemens PCS7 Allen-Bradley PLC or Wonderware.

• In-depth knowledge of FDA 21 CFR Part 11 GAMP5 and automation validation principles.

Soft Skills:

• Exceptional problem-solving and project management skills with a proven track record of delivering complex automation projects.

• Strong attention to detail and commitment to quality in a regulated environment.

• Excellent interpersonal teamwork and communication skills (both oral and written).

• Self-motivated with strong organizational skills and the ability to manage multiple priorities.

Preferred Qualifications

• Experience with computer system validation (CSV) and risk-based approaches under GAMP5.

• Proven involvement in regulatory audits/inspections (e.g. FDA EMA).

• Expertise in single-use bioprocessing technologies and integration with automation systems.

• Familiarity with Industry 4.0 IoT MES (Manufacturing Execution Systems) or data analytics platforms for process optimization.

• Experience working on global teams or Centers of Excellence (CoE).

• Knowledge of predictive maintenance real-time process monitoring or machine learning applications in bioprocessing.

• Proficiency in additional programming languages or tools (e.g. Python SQL VBA) for automation scripting or data analysis.

Travel & Flexibility

• Occasional travel to our JEB Toulouse site (France) to support global alignment and collaboration.

• Flexible working hours to accommodate collaboration with European teams across time zones.

Why Join Just-Evotec Biologics

• Impact Lives Globally: Play a pivotal role in making biotherapeutics more accessible through innovative automation solutions.

• Cutting-Edge Technology: Work with state-of-the-art DeltaV systems and next-generation bioprocessing platforms like .

• Collaborative Culture: Join a diverse global team of experts in a dynamic fast-paced environment.

• Career Growth: Take on leadership opportunities in a rapidly growing organization committed to advancing biomanufacturing.

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#BeCUREious and explore the endless possibilities at Just Evotec Biologics!

The base pay range for this position at commencement of employment is expected to be $112560 to $154100; Base salary offered may vary depending on the 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.