Commissioning Lead – DeltaV Process System Migration

Commissioning Lead – Emerson DeltaV Process System Migration (Pharma) Assignment Overview We are looking for a senior Commissioning Lead to support a large-scale process control system migration project in a GMP-regulated pharmaceutical manufacturing environment. The assignment is fully on-site and involves leading commissioning activities within a defined process area in a complex production facility. You will take ownership of your scope from planning through execution, working closely with CQV, Automation, and Operations in a cross-functional project organization. Key Responsibilities Lead and coordinate commissioning activities within an assigned process area

Define and execute a risk-based test strategy based on process requirements and functional design specifications

Perform functional and scenario-based testing across multiple software and batch control levels

Identify, document, and track issues and deviations

Coordinate re-testing and verification of fixes together with Automation and CQV teams

Support development and execution of IQ/OQ test scripts

Participate in operational test runs and performance qualification activities

Support operators during test execution and handle deviations

Provide structured daily status reporting and risk escalation

Plan test windows and resource needs for your commissioning scope

Required Experience Proven experience commissioning pharmaceutical or API manufacturing facilities

Strong background in DCS / PLC / SCADA systems in regulated environments

Experience working in large and complex plant environments

Good knowledge of GMP and data integrity principles (ALCOA+)

Familiar with change control, deviation handling, and qualification processes

Hands-on DeltaV experience is strongly preferred

Ability to troubleshoot and verify control system configuration efficiently

Personal Profile Proactive and self-driven

Clear and structured communicator

Analytical and solution-oriented

Comfortable balancing quality, timeline, and risk in GMP projects

Effective in cross-functional project teams