Associate Manufacturing Engineer

at  Radiometer

In our line of work, life isn’t a given - it’s the ultimate goal. When life takes an unexpected turn, our technology and solutions enable caregivers to make informed diagnostic decisions to improve patient care. This is our shared purpose at Radiometer and what unites all +4000 of us - no matter our roles or where in the world we’re located. Creating impactful innovations like ours, doesn’t happen overnight - it requires uncompromising persistency, passion, and a desire to make a difference. Here, you can learn, grow, and chart an uncommonly diverse career.
Radiometer is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we’re working at the pace of change to improve patient lives with diagnostic tools that address the world’s biggest health challenges.
You will be a part of the Automation & Assembly team with 11 friendly and helpful colleauges. As an Associate Manufacturing Engineer, your main responsibility is commisioning of new automated equipment and optimizing of existing production processes. You will be responsible for validation activities for small and larger projects within manufacturing, supporting the projects from the early idea and scoping phase, right to the end where the project is implemented and sustained.
The core project teams often consist of 2-3 colleagues and a lot of satellite stakeholders. It is important that you thrive in a technical environment, but a lot of the work are related to hands-on in the preparation of documentation e.g., User Requirement Specification, Validation Protocols and Test Plans or participating in technical studies.

THE ESSENTIAL REQUIREMENTS OF THE JOB INCLUDE:

• Minimum bachelor’s degree in mechanical engineering, automation, or a related field.
• 0-3 Years of experience.
• Can understand and analyze technical topics and problems.
• Can work structured and super focused with technical documentation.
• Set a pride in Good Documentation Practice.
• It is a plus if you have knowledge about GMP & Medical Devices.
• Fluency in both verbal and written English is a must, Fluency in Danish is a plus.
• Possess a strong personal drive, be well-organized and have excellent communication skills.

• Work with various automation projects within manufacturing, right from idea to implementation.
• Be responsible for validation activities, including preparing documentation User Requirement Specification, Validation Protocols and Test Plans.
• Hands-on experience with commisioning of machines.
• Learn and take the first steps into your career!
• Be a part of a fun and innovative team!