Principal Automation Engineer – DeltaV Specialist, GxP Biologics Manufacturing

Evotec

Principal Automation/Process Control Engineer driving DeltaV automation initiatives in GxP biologics manufacturing. Leading design and implementation for Just-Evotec’s innovative J.POD continuous manufacturing platform.

Posted 7/29/2026full-timeRedmond • Washington • 🇺🇸 United StatesLead💰 $140,000 - $170,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in DeltaV process control systems, GxP compliance, and automation validation within the pharmaceutical and biotech industries. Proven ability to lead projects, collaborate across teams, and drive continuous improvement initiatives.

Highest-signal resume keywords

DeltaV Process Control DesignGxP Compliance ExpertiseAutomation Validation PrinciplesProject Management for PCS ImplementationCollaboration with Cross-Functional Teams

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

DeltaV ProgrammingAutomation Control System DesignSystem IntegrationTechnical TroubleshootingProcess Optimization

Soft Skills

LeadershipCollaborationCommunication

Tools & Technologies

Emerson DeltaVSiemens PCS7Allen-Bradley PLCWonderware

Industry Keywords

Pharmaceutical IndustryBiotech IndustryLife SciencesGxP-Regulated EnvironmentsFDA 21 CFR Part 11GAMP5

Tech Stack

Tools & technologies

SDLC

About the role

Key responsibilities & impact

Lead Automation Innovation: Design and implement advanced DeltaV process control schemes to enhance the J.POD continuous manufacturing platform
Maintain Global Standards: Oversee the global validated DeltaV library, establish governance, and manage change control to ensure consistency across Just-Evotec’s manufacturing network
Drive Strategic Initiatives: Contribute to the global Software Development Life Cycle (SDLC) and roadmap for DeltaV, aligning automation strategies with business objectives
Collaborate Globally: Partner with Site MSAT Automation teams, process engineers, data scientists, quality assurance, and validation teams to support global and site-specific goals
Ensure GxP Compliance: Develop and execute detailed specifications, IQ/OQ/PQ protocols, SOPs, and training materials in compliance with FDA 21 CFR Part 11 and GAMP5 guidelines
Troubleshoot and Optimize: Lead technical root cause analyses, incident investigations, and troubleshooting for process control and automation infrastructure issues
Support Manufacturing Operations: Provide hands-on technical expertise to manufacturing sites for DeltaV systems, automation infrastructure, and process optimization
Manage Projects: Oversee Process Control System (PCS) implementation projects with third-party suppliers/integrators, ensuring timely and successful delivery
Continuous Improvement: Drive operational enhancements by integrating automation with single-use technologies, predictive analytics, and Industry 4.0 principles

Requirements

What you’ll need

Bachelor’s or Master’s degree in Engineering, Computer Science, or related field with 10+ years of relevant experience; OR Associate’s degree in a science-related field with 13+ years of relevant experience
5+ years in pharmaceutical, biotech, or life sciences industries, with a focus on GxP-regulated environments
Advanced proficiency in Emerson DeltaV (SCADA/DCS) for bioprocessing, including coding, configuration, and system integration
Strong background in designing, installing, programming, and validating automated control systems
Familiarity with other automation platforms such as Siemens PCS7, Allen-Bradley PLC, or Wonderware
In-depth knowledge of FDA 21 CFR Part 11, GAMP5, and automation validation principles

Benefits

Comp & perks

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
paid holiday
wellness and transportation benefits