Hi,
My name is Dipak Kumar , and I am reaching out from Resource Logistics . I came across your profile and wanted to reach out regarding an exciting opportunity for a Senior Automation Engineer @ Muskegon, MI (Hybrid) If you are interested in the role below, please share your updated resume along with your best time to connect so we can discuss the opportunity further.
Title: Senior Automation Engineer (Only W2 profiles)
Duration: 6+ Months
Location: Muskegon, MI
• Role requires a senior level automation engineer to be comfortable operating independently while supporting others.
• No CSV authorship responsibility: CSV activities are supported indirectly through automation execution and issue resolution.
• DeltaV DCS automation experience in pharmaceutical / biopharma manufacturing (DeltaV Batch experience is a must, not Continuous DeltaV)
• Strong troubleshooting and problem-solving skills in live manufacturing environments, including commissioning, issue triage, and rapid resolution under GMP constraints
• Deep understanding of biopharma regulatory expectations (GMP, validation, ISA 88, GAMP) and ability to apply them during real time plant execution
Job Description
• Serve as an onsite DeltaV Automation Engineer supporting C&Q execution activities.
• Work independently to troubleshoot, configure, and support DeltaV control system logic, phases, and automation components during C&Q.
• Provide technical mentorship and guidance to junior engineers and inter,te engineers, answering questions and supporting issue resolution in real time.
• Support C&Q activities including test execution support, issue investigation, re,tion, and retest preparation related to automation scope.
• Collaborate closely with Cognizant and client teams onsite to ensure automation behavior aligns with approved Functional Specifications and test expectations.
• Respond to automation-related questions arising during commissioning and qualification activities.
• Identify automation issues, propose technical solutions, and support implementation under change control where required.
• Maintain compliance with applicable GMP requirements and site procedures during onsite execution.