What you will work on:

• Support the development department in ensuring quality and compliance in medical device projects.
• Coordinate and follow up on the “Management System Plan” to align with development activities.
• Define and oversee training processes, ensuring agreements and quality standards are met.
• Act as a key advisor to R&D project managers, process owners, and stakeholders.
• Communicate with external parties, ensuring proper training and compliance within development projects.

What you bring:

• Fluent in Swedish and English, both spoken and written.
• Solid knowledge and experience in CAPA processes within medical device manufacturing.
• Experience in outsourcing development activities, including quality agreements and competence assurance.
• Strong organizational skills with the ability to manage multiple tasks and coordinate effectively across teams.