DeltaV Automation Lead GMP Biopharma C&Q

Role requires a senior level automation engineer 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

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

JD:
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 intermediate engineers, answering questions and supporting issue resolution in real time.
Support C&Q activities including test execution support, issue investigation, remediation, and re test 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.