Senior DeltaV Automation Engineer – Biopharma GMP

Intone Networks Inc; Michigan; On-site; USD 110,000 - 140,000; Full time

Job summary

Intone Networks Inc. in Muskegon, MI is seeking a Senior Automation Engineer to lead DeltaV automation activities in GMP biopharma environments. You will troubleshoot, configure, and support DeltaV control logic onsite, mentor junior engineers, and collaborate with client teams to ensure compliance with specifications.

The role requires strong problem-solving in live manufacturing, C&Q support, and adherence to GMP, ISA-88, and GAMP standards with strong regulatory awareness.

Qualifications

• Senior level automation engineer with capability to work independently.
• DeltaV Batch experience is a must (not Continuous DeltaV).
• Strong understanding of GMP, validation, ISA 88, and GAMP.

Responsibilities

• Serve as an onsite DeltaV Automation Engineer supporting C&Q execution activities.
• Troubleshoot, configure, and support DeltaV control system logic during C&Q.
• Provide technical mentorship to junior/intermediate engineers and aid issue resolution in real time.
• Support C&Q activities including test execution, investigation, remediation, and re-test preparation.
• Collaborate with Cognizant and client teams onsite to ensure automation aligns with specs and test expectations.
• Respond to automation questions during commissioning and qualification.
• Identify automation issues and propose solutions under change control.
• Maintain GMP compliance and site procedures during onsite execution.

Skills

DeltaV automation

GMP compliance

Troubleshooting

Regulatory knowledge

Mentoring

Tools

DeltaV DCS

Job description

Intone Networks Inc. in Muskegon, MI is seeking a Senior Automation Engineer to lead DeltaV automation activities in GMP biopharma environments. You will troubleshoot, configure, and support DeltaV control logic onsite, mentor junior engineers, and collaborate with client teams to ensure compliance with specifications.

The role requires strong problem-solving in live manufacturing, C&Q support, and adherence to GMP, ISA-88, and GAMP standards with strong regulatory awareness.