Automation Engineer Site Based, Redmond, WA

Job Title: Automation Engineer

Shifts: Days Monday to Friday.

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 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 #BeCurious with us and see where your curiosity can take you!

The Role: / your challenge in our journey

Were looking for a passionate and curious Automation Engineer with a primary focus on Manufacturing Execution Systems (MES) to join our 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 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.

What Youll Do:

1. MES Design & Implementation

• 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)

2. Automation & Process Control Support

• 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

3. Manufacturing Support & System Ownership

• 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

4. Compliance Validation & Documentation

• 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

5. Project Execution & NPI Support

• 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

6. Continuous Improvement & Digital Manufacturing

• 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

7. Technical Contribution & Collaboration

• 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

Who You Are:

• Bachelors 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

Preferred

• 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

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. Note this role is site based.

• 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.

• 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

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 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 $92400 to $126500;this is a salary exempt role. 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 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.