Regulatory Affairs MDR Engineer - Page Group : Job Details

Fantastic opportunity to join a dynamic team launching innovative technology within the medical technology sector.

Client Details

My client is an innovative medical devices manufacturer based in London, England.

Description

Quality Management - following process and procedures in compliance with ISO13485/MDR QMS system

Design support - team member with contributory role to new product design

Profile

Good understanding of reporting requirements under MDR/ISO-13485

Flexibility and Resilience

Quality objectives- The desire to meet the needs and expectations of regulatory compliance and product quality

Job Offer

Competitive package available