VIE - Industrialization Engineer - Oslo

As a trusted partner, our Public Health mission is to make food systems safer, healthier and more sustainable. Throughout our global network in 27 countries, we offer to our customers a wide range of testing and innovative solutions dedicated to preventing health risks related to food, environment and consumer goods. External growth has been a key pillar of our history with more than 40 acquisitions completed in the last 10 years.

If you want to contribute to an inspiring long-term purpose, to be part of a fast growing company on a high-value market with significant build-up opportunities, and to grow in an entrepreneurial and warm environment, join us!

Position Summary:

The Industrialization Engineer plays a central role in ensuring robust, compliant, and efficient manufacturing processes within a regulated environment. The role drives quality improvement initiatives through CAPA management, process validation, risk analysis, and the implementation of changes, while supporting cross-functional teams in maintaining compliance and operational excellence.

Key responsibilities:

• Facilitate change control, implementation, and continuous improvement initiatives.

• Plan and execute industrialization activities, including process validation and qualification.

• Conduct process risk assessments and support risk mitigation activities.

• Lead CAPA and nonconformance investigations, including root cause analysis.

• Support compliance with Quality Management System (QMS) and regulatory requirements.

• Collaborate with Manufacturing, Quality, Supply Chain, and Engineering teams to improve process performance.

Your profile:

• You hold a degree in Engineering or a related technical discipline, preferably in Mechanical, Electrical, or Mechatronics Engineering.

• You have a strong understanding of manufacturing processes and solid experience with Quality Management Systems (QMS), CAPA, nonconformance handling, and change management.

• Experience in a regulated industry, such as Medical Devices, IVD, or Pharmaceuticals, is preferred. Knowledge of validation, process qualification, and risk management methodologies would be an advantage.

• You are structured and analytical, with strong problem-solving skills, a quality-focused approach, and a continuous improvement mindset.

• You have strong communication and facilitation skills, enabling you to drive implementation and build alignment across functions.

• You are fluent in English.

Desired start date: January or February 2026
Duration: One year