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Cyprotex

Principal Automation/Process Control Engineer DeltaV Specialist - Redmond, WA

Cyprotex, Seattle, Washington, us, 98127

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Overview

Job Title:

Principal Automation/Process Control Engineer DeltaV Specialist (GxP Biologics Manufacturing) - Global MSAT Location:

Redmond, WA Department:

Global MSAT Reports To:

Director, Automation At Evotec, we believe that curiosity is the spark that drives innovation and success. We are a forward-thinking team that thrives on challenging the status quo, learning from each other, and pushing the boundaries of whats possible. Were on a mission to create a place where curiosity isnt just encouragedits celebrated. Are you someone who asks questions, seeks answers, and isnt afraid to go deeper?

#BeCureious

with us and see where your curiosity can take you! The Role

Were looking for a passionate and curious

Principal Automation/Process Control Engineer

to join our team. In this role, youll drive impactful projects, collaborate with bright minds, and explore uncharted territories. Youll lead DeltaV-based process control systems (SCADA and DCS) for cGMP biologics manufacturing facilities and help standardize across the J.POD network, tackling complex technical challenges in a highly regulated environment. As a

Principal Automation/Process Control Engineer

at Evotec, youll ask hard questions, think creatively, and implement solutions that push us forward. This role supports global manufacturing efficiency, regulatory compliance, and continuous improvement in biomanufacturing. Are you an Automation Engineer with deep expertise in

Emerson DeltaV

and a drive to innovate in biologics manufacturing? This role is based in Redmond, WA and is part of the Global Manufacturing Sciences and Technology (GMSAT) team to lead automation initiatives, enhance the J.POD platform, and improve global access to biotherapeutics in a GxP-regulated environment. Responsibilities include leading design, implementation, and optimization of

DeltaV-based process control systems (SCADA and DCS) , collaborating globally to ensure standardization, and driving operational excellence in a regulated setting. A background in

bioprocessing automation ,

GAMP5 validation , and

FDA compliance

is required. Responsibilities

Lead Automation Innovation : Design and implement advanced

DeltaV process control schemes

to enhance the J.POD continuous manufacturing platform, including batch tracking, process control limits, predictive control algorithms, and real-time data integration.

Maintain Global Standards : Oversee the global

validated DeltaV library , establish governance, and manage change control to ensure consistency across Just-Evotecs 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.

Qualifications

Who You Are: Education & Experience : Bachelors or Masters degree in Engineering, Computer Science, or related field with

10+ years

of relevant experience;

OR

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 .

Technical Expertise : 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.

Soft Skills : 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.

Preferred Qualifications Experience with

computer system validation (CSV)

and risk-based approaches under

GAMP5 .

Proven involvement in

regulatory audits/inspections

(e.g., FDA, EMA).

Expertise in

single-use bioprocessing technologies

and integration with automation systems.

Familiarity with

Industry 4.0 ,

IoT ,

MES (Manufacturing Execution Systems) , or

data analytics platforms

for process optimization.

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.

Travel & Flexibility Occasional travel

to our JEB Toulouse site (France) to support global alignment and collaboration.

Flexible working hours

to accommodate collaboration with European teams across time zones.

Why Join Just-Evotec Biologics? 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.

Are You Still Curious? If youve read this far, then chances are youve got a curious mindjust like us. So, what are you waiting for? Take the leap and apply today. We cant wait to see where your curiosity leads youand how it will shape the future of

Evotec Let your curiosity guide your career #BeCUREious

and explore the endless possibilities at Just Evotec Biologics! The base pay range for this position at commencement of employment is expected to be $112,560 to $154,100; Base salary offered may vary depending on the individuals 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, flexible work, 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. #J-18808-Ljbffr