Automation Engineer

HW3; København; On-site; DKK 400.000 - 600.000; Full time

Job summary

A leading pharmaceutical automation firm in Copenhagen is seeking an experienced DeltaV Engineer to join a key automation project. The role involves designing and implementing DeltaV systems, troubleshooting control systems, and collaborating with cross-functional teams. Candidates should have over 7 years of experience in regulated environments and strong GMP knowledge. This is a full-time on-site position with a competitive hourly rate.

Benefits

Long-term contract opportunity

Competitive hourly rate

On-site role with potential for extension

Qualifications

• Minimum 7 years’ experience with DeltaV in pharma/biotech or similar regulated industries.
• Hands-on experience with commissioning, validation, and troubleshooting.
• Ability to work on-site in Denmark.

Responsibilities

• Design, configuration, and implementation of DeltaV systems.
• Troubleshooting and maintaining control systems.
• Collaborating with cross-functional teams.
• Supporting commissioning and validation activities.

Skills

DeltaV systems expertise

GMP environments knowledge

Communication skills

Problem-solving skills

Job description

Automation Engineer – DeltaV Engineer: Pharmaceutical Automation

HW3 Copenhagen, Capital Region of Denmark, Denmark

DeltaV Engineer: Pharmaceutical Automation

We’re looking for an experienced DeltaV Engineer to join a leading pharmaceutical automation project in Denmark.

What’s on offer:

• Long-term contract opportunity
• Competitive hourly rate
• On-site role with potential for extension

The role:

You will play a key role in supporting automation and process control within a GMP-regulated environment. Responsibilities include:

• Design, configuration, and implementation of DeltaV systems
• Troubleshooting and maintaining control systems to ensure compliance and efficiency
• Collaborating with cross-functional teams (engineering, QA, operations)
• Supporting commissioning, validation, and documentation activities
• Ensuring system reliability and adherence to industry regulations

What we’re looking for:

• Minimum 7 years’ experience with DeltaV in pharma/biotech or similar regulated industries
• Strong knowledge of GMP environments and automation lifecycle
• Hands-on experience with commissioning, validation, and troubleshooting
• Excellent communication and problem-solving skills
• Ability to work on-site in Denmark

Seniority level

• Mid-Senior level

Employment type

• Full-time

Job function

• Industries

Industries

• Pharmaceutical Manufacturing
• Biotechnology Research
• Medical Equipment Manufacturing