Overview: Responsibilities:

• 
  Integrate production processes early in the development phase: Ensure that production processes are considered from the beginning of development projects.
• DFMA (Design for Manufacturing and Assembly): Implement DFMA principles to optimize the production and assembly of new products.
• Specification and qualification of equipment: Develop specifications and qualify production equipment for new products.
• Process risk analysis: Conduct risk analyses of production processes to identify and mitigate potential issues.
• Understanding process characteristics: Analyze and understand process characteristics to improve and optimize production processes.
• Development of test methods: Design and develop test methods to ensure product quality and performance.
• Control of FAT/SAT activities: Oversee Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT) activities to ensure equipment meets required standards.
• Collaboration with Manufacturing Engineering: Work closely with Manufacturing Engineering to ensure the transfer of robust processes to production.
• Project Management: Take responsibility and ownership of large sub-tasks and ensure their successful completion.

Qualifications:

• Brings a degree in engineering, not specific to any scientific area.
• Has experience with production processes and development.
• Possesses statistical knowledge, beneficial for DOE (Design of Experiments) and process validation tasks.
• Has knowledge of the medical device industry or other regulated industries (a plus but not required).
• Is patient and persistent, thriving in projects with long timelines and industry-specific requirements.
• Is proud of their work but also pragmatic, and able to collaborate in a team with diverse expertise.
• Brings solid communication skills in Danish and English, both written and oral.
• Is a true team player.