Regulatory Affairs MDR Engineer
Michael Page London
About Our Client
My client is an innovative medical devices manufacturer based in London, England.
Job 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
The Successful Applicant
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
What's on Offer
Competitive package available
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