Technical Consultant – DeltaV (Commissioning Engineer)

03-07-2025
Job Type
Contract
Emp Type
Full Time
Industry
Construction and Engineering
Functional Expertise
Any
Salary Type
Hourly
Salary
Negotiable

Job Description

Technical Consultant – DeltaV (Commissioning Engineer) – Södertälje, Stockholm

Contract Duration: 12 Month Contract

Full Time on Site

IMMEDIATE START AND MUST RELOCATE TO SWEDEN

A growing SME within Life Sciences manufacturing technology is seeking experienced Technical Consultants to join its team and support ongoing DeltaV projects on a leading pharmaceutical site in Sweden.

Key Responsibilities:

  • Design, develop, and support commissioning of DCS systems, primarily Emerson DeltaV, for pharmaceutical manufacturing.
  • Implement automation solutions aligned with ISA-88 (S88) batch standards.
  • Design and qualify both Physical and Procedural Layers for process automation systems.
  • Collaborate with automation teams on system architecture, design specifications, control strategies, and library creation.
  • Provide day-to-day support for DeltaV operations, including troubleshooting and performance improvements.
  • Support investigations (NCs/CAPAs), identify root causes, and implement corrective actions.
  • Carry out field commissioning and offer system administration/maintenance assistance.
  • Contribute to computer system validation (CSV) and automation documentation.
  • Liaise with Operations, Process Engineering, Equipment Vendors, and Technology Providers.

Requirements:

  • 10–12 years’ experience in automation/commissioning roles, ideally within the pharmaceutical sector.
  • Proven track record in designing and commissioning DeltaV DCS systems for GMP manufacturing environments.
  • Strong knowledge of batch automation and ISA-88 standards (control modules, equipment modules, phases, units, recipes).
  • Familiarity with biopharma processes and GMP requirements.
  • Solid understanding of automation hardware and networking.
  • Emerson DeltaV Batch experience is essential.
  • Comfortable working within SDLC frameworks and pharmaceutical quality systems.
  • Strong communication and coordination skills for cross-functional collaboration.

 

Consultant