On-Site Process Automation Engineer (DeltaV & GMP)

ACL Digital

Thousand Oaks (CA)

On-site

USD 62,000 - 68,000

Full time

14 days+
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Job summary

ACL Digital seeks an External Automation Engineer in Thousand Oaks, CA to augment our MCS F&E Automation team. This on-site role focuses on updating, maintaining, and improving DeltaV automation systems and providing critical site support for ongoing biological processes.

The ideal candidate will have strong analytical and collaborative skills, experience with manufacturing process controls, and a track record of operating in cross-functional teams within GMP environments.

Qualifications

  • Degree in Electrical Engineering or Computer Science, Chemical Engineering or Biotech Engineering.
  • Extensive programming, design, installation and lifecycle management of manufacturing process controls and automation.
  • Experience developing process control strategies for NPI and technology deployment in drug substance operations.
  • Knowledge of automation design and troubleshooting in GMP biopharma facilities and related equipment/systems.
  • Experience driving continuous improvements in safety, reliability and productivity in drug substance operations.
  • 5+ years of experience with Rockwell Automation SCADA/PLC, electronic batch reporting, and process control systems.

Responsibilities

  • Update, maintain, and improve DeltaV automation systems.
  • Provide critical site support for ongoing biological processes.
  • Collaborate in cross-functional teams and maintain regulatory compliance.

Education

Electrical Engineering
Computer Science
Chemical Engineering
Biotech Engineering

Tools

Rockwell Automation SCADA/PLC
OPC
Foundation Fieldbus
Profibus
DeviceNet
Electronic Batch Reporting

Job description

ACL Digital seeks an External Automation Engineer in Thousand Oaks, CA to augment our MCS F&E Automation team. This on-site role focuses on updating, maintaining, and improving DeltaV automation systems and providing critical site support for ongoing biological processes.

The ideal candidate will have strong analytical and collaborative skills, experience with manufacturing process controls, and a track record of operating in cross-functional teams within GMP environments.

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