Jobs · Engineering · Pennsylvania

Sr. Automation Engineer

ZETA · King of Prussia, PA · 2 wk ago
EngineeringFull-time

About the role

This is a senior-level role for someone who thrives in a hands-on, fast-moving environment and enjoys implementing solutions on real equipment. You’ll lead automation projects for major biotech and pharmaceutical clients, working across brownfield integrations (about 70% of our work) and greenfield builds. You’ll own everything from design through commissioning, and you’ll be the person our clients trust when they need a system to work reliably in a GMP environment. If you enjoy variety, collaboration, and the chance to work with multiple platforms and technologies, this is the kind of role where you’ll never be bored.

Responsibilities

  • Lead the design, implementation, commissioning, and startup of automation and control systems for biotech and pharmaceutical processes.
  • Integrate new equipment into existing manufacturing systems and lead greenfield automation builds.
  • Develop, review, and troubleshoot automation code, functional specs, and system architecture.
  • Write and execute GMP-compliant commissioning, qualification, and validation documentation.
  • Serve as a technical leader on client projects, guiding internal teams and mentoring junior engineers.
  • Work directly on customer sites to diagnose issues, optimize performance, and support production.
  • Collaborate with process, equipment, and CQV teams to ensure seamless project delivery.
  • Contribute to building internal standards, best practices, and scalable processes as our team grows.

Requirements

  • Bachelor’s degree in Engineering, Computer Science, or a related technical field.
  • 7–12 years of experience in automation/controls engineering within biotech, pharma, or medical device manufacturing.
  • Strong experience with Rockwell Automation (PLC, SCADA, FactoryTalk).
  • Experience with DeltaV or the ability to learn it quickly.
  • Deep understanding of S88 batch concepts and process automation fundamentals.
  • Mandatory GMP experience, including writing and executing qualification protocols.
  • Experience with databases (SQL Server), industrial networks/OT, and plant-floor interfaces.
  • Familiarity with equipment such as bioreactors, filtration skids, CIP/SIP systems, and hygienic utilities.
  • Ability to work independently, manage client expectations, and lead technical decision-making.
  • Willingness to travel as needed and be on-site in King of Prussia at least 3 days per week.

Benefits

  • Competitive PTO & vacation
  • Free coffee
  • Medical, Dental, & Vision Health Benefits
  • 401K with 5% employer match of annual salary
  • Travel & training opportunities

Start date: 07.09.2026

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