Principal Automation Engineer – DeltaV Specialist, GxP Biologics Manufacturing

• 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

• 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

Highest-signal resume keywords

• DeltaV Process Control Design
• GxP Compliance Expertise
• Automation Validation Principles
• Project Management for PCS Implementation
• Collaboration with Cross-Functional Teams

ATS Optimization Keywords

Hard Skills

• DeltaV Programming
• Automation Control System Design
• System Integration
• Technical Troubleshooting
• Process Optimization

Soft Skills

• Leadership
• Collaboration
• Communication

Industry Keywords

• Pharmaceutical Industry
• Biotech Industry
• Life Sciences
• GxP-Regulated Environments
• FDA 21 CFR Part 11
• GAMP5

Tools & Technologies

• Emerson DeltaV
• Siemens PCS7
• Allen-Bradley PLC
• Wonderware

Core Competencies

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.