DeltaV Process Automation Engineer – Pharma (GMP)

Wunderlich-Malec Engineering, Inc; Calabasas (CA); On-site; USD 120,000 - 180,000; Full time

Job summary

Wunderlich-Malec Engineering, Inc. in Calabasas, CA, is seeking a Process Automation Engineer to design, implement and maintain DeltaV-based solutions for pharmaceutical processes.

You will work with cross-functional teams to translate requirements into technical specifications and ensure GMP-compliant validation. Responsibilities include integrating DeltaV with equipment, developing control strategies, configuring OPC/Modbus interfaces, and conducting IQ/OQ/PQ testing.

Qualifications

• BS in Electrical or Chemical Engineering (preferred).
• Experience with DeltaV-based automation for pharma/biotech environments.
• Strong knowledge of FDA GMP and GAMP regulatory expectations.
• Ability to design, test, and document validation protocols (IQ/OQ/PQ).

Responsibilities

• Designs, implements, and maintains DeltaV-based process automation solutions for pharmaceutical processes.
• Collaborates with cross-functional teams to translate requirements into technical specifications.
• Integrates DeltaV systems with process equipment and control devices for seamless operation.
• Develops control strategies and sequences using DeltaV programming languages (e.g., FBD, Sequential Function Charts).
• Configures OPC/Modbus communications for interfacing with third-party devices.
• Conducts testing and validation per GMP guidelines (IQ/OQ/PQ).
• Provides technical support and troubleshooting for DeltaV systems and alarms.
• May lead project workstreams and interface directly with clients.

Skills

DeltaV automation

DeltaV Function Blocks

Control Studio

ISA-88

Regulatory compliance

Education

BS in Electrical or Chemical Engineering

Tools

DeltaV Control Studio

DeltaV Function Blocks

Job description

Wunderlich-Malec Engineering, Inc. in Calabasas, CA, is seeking a Process Automation Engineer to design, implement and maintain DeltaV-based solutions for pharmaceutical processes.

You will work with cross-functional teams to translate requirements into technical specifications and ensure GMP-compliant validation. Responsibilities include integrating DeltaV with equipment, developing control strategies, configuring OPC/Modbus interfaces, and conducting IQ/OQ/PQ testing.