Automation/Process Controls Engineer - Site MSAT, Redmond, WA
Listed on 2026-01-19
-
Engineering
Process Engineer, Automation Engineering, Electrical Engineering, Manufacturing Engineer
Job Title:
Automation/Process Controls Engineer - Site MSAT, Redmond, WA
Job Title: Automation/Process Controls Engineer - Site MSAT, Redmond, WA
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? #Be Cureious 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 ( Delta
V ) 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 Delta
V 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 .
- Participate in the design and implementation of automation and process control schemes to NPI processes, batch tracking, establishing process control limits, and applying predictive control algorithms.
- Maintain site level validated Delta
V library and participate at the site level governance and change management system for GMP changes and NPI implementation - Participate in engagement with global 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.
- Lead CAPAs and change controls, and work closely with the site MTS (Manufacturing technical services) team to implement changes
- Participate as a core team member on the NPI team to ensure all the automation changes/ MES changes are designed/tested as part of NPI readiness.
- Provide technical support to the manufacturing sites as needed, specific to process control and automation systems
- B.S or M.S. in Electrical Engineering or Computer Science, Chemical Engineering, Biotech Engineering, or related life science engineering.
- 4+ years relevant experience in pharmaceutical, biotech, or life sciences
- Strong control system automation background.
- Good understanding of design, installation, programming, and validation of automated processes.
- 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
- Candidate must possess strong focus on quality and attention to detail
- Motivated, self-starter with strong organizational skills
- Occasional travel for global alignment.
- Flexible hours to accommodate collaboration with European teams.
Preferred Qualifications
- 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,…
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