Automation Engineer - Site Based, Redmond, WA

Evotec • Redmond, WA

1d • Onsite

About The Position

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? #BeCurious with us and see where your curiosity can take you! We’re looking for a passionate and curious Automation Engineer with a primary focus on Manufacturing Execution Systems (MES) to join our team. In this role, you will support the design, implementation, and optimization of MES solutions in a GMP-regulated biotech manufacturing environment, while also contributing to broader automation and process control initiatives. This is a hands-on technical position focused on delivering reliable, compliant, and scalable MES solutions that enable efficient batch execution, electronic batch records (EBR), and end-to-end manufacturing traceability. In addition to MES ownership, you will play a supporting role across site automation systems, including process control platforms (e.g., DeltaV), SCADA/DCS systems, and integration with shop floor and enterprise systems. As an Automation Engineer at Just Evotec Biologics, you will independently execute complex MES work, own system components and workstreams, and collaborate closely with Manufacturing, MSAT, Quality, IT, and global automation teams. You will support both ongoing operations and new product introduction (NPI), while contributing to continuous improvement and digital manufacturing efforts. This role sits at the intersection of MES and automation, helping ensure seamless integration between batch execution systems and process control, while supporting a flexible, scalable, and modern manufacturing platform.

Requirements

• Bachelor’s degree in Engineering, Computer Science, or related technical field
• 5+ years of experience supporting or implementing MES in biotech, pharmaceutical, or other GxP-regulated environments
• Hands-on experience with MES platforms (e.g., Werum PAS-X, Emerson Syncade, Rockwell PharmaSuite, Siemens OpCenter, or similar)
• Experience building or supporting electronic batch records (EBR)
• Strong understanding of GMP, FDA regulations, and 21 CFR Part 11
• Experience supporting MES in a live manufacturing environment
• Working knowledge of process control systems (e.g., DeltaV, SCADA/DCS) and automation integration
• Strong troubleshooting, analytical, and problem-solving skills

Nice To Haves

• Experience supporting clinical and/or commercial manufacturing
• Familiarity with ISA-88 and ISA-95 standards
• Experience integrating MES with systems such as DeltaV, LIMS, SAP, or historians
• Experience with validation methodologies CSV and GAMP5
• Exposure to automation platforms such as DeltaV, Siemens, Allen-Bradley, or Wonderware
• Experience supporting NPI and technology transfer activities
• Exposure to digital manufacturing or data integration initiatives

Responsibilities

• Design, configure, and implement MES solutions aligned with biotech manufacturing processes and GMP requirements
• Develop and maintain electronic batch records (EBR), workflows, and recipes within the MES platform
• Translate business and process requirements into functional MES configurations
• Support integration of MES with enterprise and shop floor systems (e.g., ERP, LIMS, SCADA, historians)
• Support design and implementation of process control strategies, including batch control, data acquisition, and process monitoring
• Collaborate with automation teams on DeltaV and other DCS/SCADA systems used in bioprocessing control
• Assist in maintaining validated automation systems, libraries, and standards in alignment with site and global practices
• Contribute to integration between MES and control systems to enable seamless data flow and execution
• Serve as a technical owner for assigned MES systems, modules, or functional areas
• Support GMP manufacturing operations by troubleshooting issues, performing root cause analysis, and implementing fixes across MES and automation systems
• Partner with Manufacturing and Quality teams to support batch execution, deviations, CAPAs, and process improvements
• Monitor system performance and reliability, implementing improvements as needed
• Ensure MES and automation solutions comply with GMP, FDA, and 21 CFR Part 11 requirements, with a focus on data integrity (ALCOA+)
• Author, review, and execute validation deliverables (e.g., URS, FRS, IQ/OQ/PQ) in alignment with CSV/CSA and GAMP5 practices
• Develop and maintain accurate, audit-ready documentation, including system configurations, SOPs, and training materials
• Support internal and external audits and inspections
• Lead technical workstreams or small-to-medium MES-focused projects; contribute to larger cross-functional automation initiatives
• Participate in requirements gathering, system configuration, testing, and deployment activities
• Support new product introduction (NPI) by ensuring MES and automation changes are designed, tested, and ready for manufacturing
• Collaborate with stakeholders across Manufacturing, MSAT, Quality, IT, and Automation teams
• Support implementation of digital manufacturing initiatives such as paperless manufacturing and review-by-exception
• Identify and implement opportunities to improve manufacturing efficiency, quality, and data visibility using MES and automation systems
• Contribute to system enhancements, standardization efforts, and adoption of global automation best practices
• Stay current with MES, automation tools, and industry trends
• Act as an MES subject matter resource while contributing to broader automation knowledge within the team
• Collaborate with global automation and MSAT teams to align on standards and best practices
• Provide guidance to junior engineers and support knowledge sharing
• Contribute to design reviews, troubleshooting efforts, and continuous improvement initiatives

Benefits

• Growth Opportunities: We’re a company that believes in continuous learning and development. Whether it’s professional courses, mentorship, or new projects, we’ll help you grow.
• Flexible Work Environment: We offer flexible work options to help you balance your professional and personal life.
• Inclusive Culture: We’re committed to building a diverse and inclusive environment where everyone’s voice is valued, and curiosity is encouraged.
• Innovative Projects: You’ll 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 don’t just talk about thinking outside the box—we throw the box away. If you’ve got ideas, we want to hear them.
• Direct impact on enabling compliant manufacturing of life-saving therapies
• Hands-on ownership of MES systems supporting real production environments
• Opportunities to work across MES and automation platforms, including process control systems
• Strong cross-functional and global collaboration across Manufacturing, Quality, MSAT, and Automation
• Clear growth path toward Senior and Principal engineering roles
• 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
• Generous paid time off
• Paid holiday
• Wellness benefits
• Transportation benefits

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 501-1,000 employees