Similar Jobs
See allDirector, Quality Systems & Regulatory Affairs
CEFALY Technology
US
Quality Management
Regulatory Affairs
Director, Clinical Affairs
Integer Holdings Corporation
US
Regulatory Submissions
Medical Writing
Clinical Trial Management
Global Technical Manager – Sterilization
SGS
Global
Regulatory Affairs
Team Leadership
RA Specialist
Intuitive
APAC
Regulatory Strategy
Compliance
Commercial Operations Director
Partner Company
EMEA
Sales
Business Development
Revenue Growth
Accountabilities:
- Conduct remote audits of medical device quality management systems.
- Review objective evidence and provide structured audit reports.
- Ensure audit activities follow established methodologies and regulatory principles.
Requirements:
- Bachelor’s degree in a relevant scientific or engineering discipline.
- Minimum 4 years professional experience in the medical device industry.
- Minimum 2 years auditing QMS according to ISO 13485 and EU MDR.
Benefits:
- Flexible contractor model with remote work.
- Opportunity to evaluate innovative medical technologies.
- Autonomy in managing audit assignments.
Partner Company
The partner company specializes in assessing innovative health technologies and ensuring regulatory compliance for medical devices. It operates with a quality-focused culture, valuing autonomy and regulatory expertise.