Senior Process Engineer responsible for enhancing manufacturing operations in medical device industry. Leading process capability improvements and mentoring technical staff on production floor.
About the role
- Quality Management Engineer developing optimized processes and supporting compliance in e-health at Cambio. Join a leading player in Nordic healthcare focused on enhancing patient care.
Responsibilities
- Work in the Quality Management and Regulatory Affairs team developing the Cambio Management System (CMS)
- Support and mentor Process Owners and Sub Process Owners in their continuous improvement process work
- Ensure compliance with applicable standards and relevant Product certifications
Requirements
- Good knowledge in/or have implemented ISO 13485 and/or ISO 9001
- Good knowledge in MDR EU 2017/745 and supporting standard e.g. IEC 62304, ISO 14971
- University degree or equivalent relevant work experience
- Great verbal and written Swedish and English
- Experience from Product Risk Management work
Benefits
- Employee benefits
- Opportunities for professional growth
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
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