Principal Automation/Process Control Engineer - DeltaV Specialist - Redmond, WA
New Yesterday
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 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
We're looking for a passionate and curious Principal Automation/Process Control Engineer to join our team. If you're excited by new challenges, solving complex problems, and learning every step of the way, you might just be the perfect fit. In this role, you'll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories.
As a Principal Automation/Process Control Engineer at Evotec, you'll have the freedom to ask the hard questions, think outside the box, and find creative solutions that push us forward. It's 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 J.POD® continuous manufacturing platform, and improve global access to life-changing biotherapeutics in a GxP-regulated environment.
As a key member of our automation team, you'll 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. You'll collaborate globally to ensure standardization across our J.POD network, tackle complex technical challenges, and drive operational excellence in a highly regulated environment. If you're 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 You'll Do:
- Lead Automation Innovation: Design and implement advanced DeltaV process control schemes to enhance the J.POD 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-Evotec's 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:
- Bachelor's or Master's degree in Engineering, Computer Science, or related field with 10+ years of relevant experience; OR
- Associate's 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 J.POD.
- 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 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-#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 $112,560 to $154,100; Base salary offered may vary depending on the 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.
- Location:
- Redmond
