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 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!
The Role: / your challenge, …in our journey
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.
What You’ll 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:
Required
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
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: 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. Note this role is site based.
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
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 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 $92,400 to $126,500; this is a salary exempt role. 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, 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.