Senior Automation/Process Controls Engineer – Manufacturing Process Automation - Redmond site based

Job Title: Senior Automation/Process Controls Engineer

About Us: this is who we are

At Just Evotec Biologics, 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

This role is part of the Automation team in Global MSAT that is responsible for defining the automation (DeltaV) standards for the J.POD Manufacturing platform and ensuring alignment across the J.POD network, as well as provide automation support to Just-Evotec’s manufacturing sites. This includes designing and implementing creative solutions to complex technical challenges in helping Just achieve a novel flexible and reconfigurable cGMP manufacturing facility focused on continuous processing. The role will have an advanced proficiency of DeltaV process control automation (SCADA and DCS) used for bioprocessing control as well as at least some experience in other automation platforms (ie, Siemens, Allen-Bradley, Wonderware, etc.). Experience working in a GMP environment, change control, and automation validation in accordance with GAMP5 guidelines is highly preferred.  

What You’Ll Do

• Participate in the design and implementation of automation and process control schemes to advance the state of the JPOD continuous manufacturing platform including, but not limited to batch tracking, establishing process control limits, and applying predictive control algorithms. 
• Maintain global validated DeltaV library and define the governance and global change management for the DeltaV platform to maintain alignment across the manufacturing network 
• Participate in defining global software development life cycle (SDLC) and global roadmap for DeltaV  
• Participate in engagement with Site MSAT Automation teams to support global and site objectives 
• Develop or improve detailed specification, qualification (IQ/OQ/PQ), engineering, SOP, and training documents. 
• Collaborate with multiple disciplines, including manufacturing, process engineering, process development, data scientists, utility operations, maintenance, quality assurance, and validation to implement operational improvements 
• Author and execute test scripts or validation protocols 
• Lead or contribute to technical root cause analysis, incident investigations, and troubleshooting of process control issues 
• Provide technical support to the manufacturing sites as needed, specific to process control and automation infrastructure 
• Provide project oversight or drive progress on PAS implementation projects contracted to 3rd party suppliers/integrators with some guidance from team lead 

Who You Are

Education & Experience

• Bachelor’s or Master’s degree in Engineering, Computer Science, or related field with 5+ years of relevant experience; OR
• Associate’s degree in a science-related field with 8+ years of relevant experience; OR
• High school diploma or GED with 10+ years of relevant experience.
• 2+ years in pharmaceutical, biotech, or life sciences industries in a GxP-regulated environment.
• Strong control system automation background. Design, installation, programming, and validation of automated processes is essential. 
• Understanding of FDA CFR 21 Part 11 compliance 
• Established record of successful project completions employing proven engineering and project management skills 
• Demonstrated skills coding in DeltaV 
• Motivated, self-starter with strong organizational skills. 

Travel & Flexibility

• Occasional travel to our JEB Toulouse site (France) for global alignment.
• Flexible hours to accommodate collaboration with European teams.
• Previous experience in computer software validation 
• Participation on global teams, Center of Excellence, etc. 
• Leverage expertise using GAMP5 risk-based approach when implementing changes to the validated PAS 
• Authority inspection or audit support involvement 
• Experience with single-use technologies and systems 
• Experience with Siemens, Allen Bradley, Wonderware automation platforms 
• Are You Still Curious?

Additional Preferred Qualifications

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 Just Evotec Biologics.

Let your curiosity guide your career—#BeCurious 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.