Evotec WD
Principal Automation/Process Control Engineer DeltaV Specialist - Redmond, WA
Evotec WD, Redmond, Washington, United States, 98052
**Job Title:** **Principal Automation/Process Control Engineer DeltaV Specialist (GxP Biologics Manufacturing) -** **Global MSAT**As a **Principal Automation/Process Control Engineer** at **Evotec**, you'll have the freedom to ask the hard questions, think outside the box, and find creative solutions that push us forward. Its a role where your curiosity will fuel both your personal growth and the success of the team.Are you a passionate **Automation Engineer** with deep expertise in **Emerson DeltaV****Principal Automation/Process Control Engineer** to join our Global Manufacturing Sciences and Technology (GMSAT) team in Redmond, WA. This is your chance to lead cutting-edge automation initiatives, enhance our innovative **J.POD continuous manufacturing platform**, and improve global access to life-changing biotherapeutics in a **GxP-regulated environment.*** Associates 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**.Bachelors or Masters degree in Engineering, Computer Science, or related field with **10+ years** of relevant experience; **OR*** 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.* Exceptional problem-solving and project management skills with a proven track record of delivering complex automation projects.* Strong attention to detail and commitment to quality in a regulated environment.* Excellent interpersonal, teamwork, and communication skills (both oral and written).* Self-motivated with strong organizational skills and the ability to manage multiple priorities.* Proven involvement in **regulatory audits/inspections** (e.g., FDA, EMA).* Expertise in **single-use bioprocessing technologies** and integration with automation systems.* Experience working on global teams or Centers of Excellence (CoE).* Knowledge of **predictive maintenance**, **real-time process monitoring**, or **machine learning applications** in bioprocessing.* Proficiency in additional programming languages or tools (e.g., **Python**, **SQL**, **VBA**) for automation scripting or data analysis.Experience with **computer system validation (CSV)** and risk-based approaches under **GAMP5**.Familiarity with **Industry 4.0**, **IoT**, **MES (Manufacturing Execution Systems)**, or **data analytics platforms** for process optimization.* **Impact Lives Globally**: Play a pivotal role in making biotherapeutics more accessible through innovative automation solutions.* **Cutting-Edge Technology**: Work with state-of-the-art **DeltaV systems** and next-generation bioprocessing platforms like J.POD.* **Collaborative Culture**: Join a diverse, global team of experts in a dynamic, fast-paced environment.* **Career Growth**: Take on leadership opportunities in a rapidly growing organization committed to advancing biomanufacturing.
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