Senior Validation & Qualification Engineer | Halden Pharma

Halden Pharma is currently undergoing an exciting phase of development, with increasing focus on quality, efficiency, and growth. We are now looking for a Senior Validation & Qualification Engineer to strengthen our Technical Department.

In this role, you will work hands-on with validation and qualification of equipment, facilities, and processes -- contributing directly to safe and reliable manufacturing for our international customers.

You will be part of a collaborative environment, working closely with Production, QA, QC, Engineering, Supply Chain, and project teams.

What you will be working on:

• Planning and executing qualification and validation activities for equipment, facilities, and processes
• Preparing and following up on validation plans, protocols, and reports
• Supporting installation and start-up of new equipment (FAT, SAT, commissioning)
• Collaborating with cross-functional teams to ensure efficient project execution
• Contributing to continuous improvement and standardization of validation practices

This is a varied role combining hands-on work and coordination across teams.

Who we are looking for

We are looking for someone with a technical background who enjoys working in a structured and collaborative environment.

You likely have:

• A degree in engineering, chemistry, biotechnology, or a related field
• Experience with validation, qualification, or technical processes (typically 5+ years)
• Experience from an industry with requirements for documentation and compliance
• An interest in understanding technical systems and how they work together
• A structured and practical approach to problem-solving
• Experience from the pharmaceutical or medical device industry is highly regarded and will be considered a strong advantage.

We also welcome candidates from other regulated industries with strong compliance and documentation requirements, such as food production, process industry, or similar.

Why join Halden Pharma?

• A key role in a company undergoing significant development
• Opportunities to work on advanced technical systems and processes
• A collaborative and supportive work environment
• The chance to grow your competence within GMP and validation
• Exposure to international customers and projects

If this sounds like a role where you can contribute and grow, we would very much like to hear from you.