Process engineer • fairfield ca
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The average salary range is between $ 68,500 and $ 110,000 year , with the average salary hovering around $ 84,250 year .
The average salary range is between $ 77,506 and $ 125,000 year , with the average salary hovering around $ 92,532 year .
Location: Vacaville, CA
Execute automation projects and Automation Roadmap initiatives for systems supporting Cell Culture Plant 1 (CCP1) and Cell Culture Plant 2 (CCP2). This role provides technical leadership for process control, batch execution, and manufacturing OT systems in a regulated biopharmaceutical environment to ensure operational excellence and reliable patient supply.
Support MAR activities and Vacaville Manufacturing Operations by assisting with tech transfers and capital projects while maintaining the qualified state of PLC and VSC systems.
What you will get
The full-time base annual salary for this position is expected to range between $129,000 to $219,000. In addition, below you will find a comprehensive summary of the benefits package we offer:
Performance-related bonus
Medical, dental and vision insurance
401(k) matching plan
Life insurance, as well as short-term and long-term disability insurance
Employee assistance programs
Paid time off
Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge.
What you will do
Lead the design and support of automation systems, including MCS, DCS, and PLC-based controllers.
Lead and support automation activities for capital projects, process improvements, system upgrades, and plant expansions.
Direct cross-functional teams and external vendors to ensure "right the first time" system implementations.
Oversee system testing, debugging, and startup activities for critical manufacturing assets.
Support manufacturing operations with on-call troubleshooting, root cause investigations, and continuous improvement initiatives.
Author and review automation-related documentation including design specifications, control narratives, functional specifications, test protocols, and validation documentation (IQ/OQ/PQ).
Execute both off-line and on-line coding and peer reviews to maintain system integrity and compliance.
What we are looking for
Bachelor’s degree Engineering, or related field preferred.
Effective communication to engage at all levels
Ability to secure relevant information and identify key issues and relationships from a base of information.
High adaptability to changing operational conditions and requirements Proven ability to prioritize and manage key deliverables effectively
Proven experience with loop diagram development, field (or remote) device I/O integration, and end‑to‑end loop testing for biopharmaceutical process control systems. Skilled in coordinating with engineering, construction, and commissioning teams to validate signal integrity from field instrumentation through DCS/PLC systems in support of safe and compliant startup activities.
About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law.
Ready to shape the future of life sciences? Apply now.
Reference: R75735
