Commissioning Lead – DeltaV Process System Migration

WeQuel

Stockholms kommun

On-site

SEK 900,000 - 1,200,000

Full time

14 days+
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Job summary

WeQuel is seeking a senior Commissioning Lead to support a large-scale DeltaV process system migration in a GMP pharmaceutical manufacturing environment. The assignment is fully on-site within a complex production facility, and you will own scope from planning through execution.

You will work closely with CQV, Automation, and Operations in a cross-functional project organization, coordinating commissioning activities, testing, deviations, and documentation.

Qualifications

  • Proven experience commissioning pharmaceutical or API manufacturing facilities.
  • Strong background in DCS/PLC/SCADA systems in regulated environments.
  • 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

DCS/PLC/SCADA

Tools

DeltaV

Job description

Commissioning Lead – Emerson DeltaV Process System Migration (Pharma)

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
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