Commissioning Lead – DeltaV Process System Migr... Stockholm

Wequel; Stockholms kommun; On-site; SEK 900,000 - 1,300,000; Full time

Job summary

Wequel is seeking a senior Commissioning Lead to drive a large-scale DeltaV-based process system migration in a GMP-regulated pharmaceutical facility. The role is on-site in Sweden, coordinating CQV, Automation, and Operations across a defined process area.

You will own the scope from planning to execution, defining risk-based test strategies, and leading IQ/OQ test script development, test execution, and issue resolution with cross-functional teams.

Qualifications

• Proven experience commissioning pharmaceutical or API manufacturing facilities
• Strong background in DCS/PLC/SCADA in regulated environments
• Experience in large, complex plant environments
• Good knowledge of GMP and data integrity principles (ALCOA+)
• Hands-on DeltaV experience strongly preferred

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

Skills

Commissioning

DeltaV

GMP compliance

Cross-functional teamwork

Problem solving

Tools

DeltaV

DCS/PLC/SCADA

Job description

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