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Regulatory Affairs MDR Engineer

Regulatory Affairs MDR Engineer

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Posted 2 days ago, valid for 23 days

London, Greater London EC1R 0WX

£60,000 - £72,000 per annum

Full Time

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Sonic Summary

Fantastic opportunity to join a dynamic team launching innovative technology within the medical technology sector.
The position is with an innovative medical devices manufacturer based in London, England.
Candidates should have a good understanding of reporting requirements under MDR/ISO-13485 and demonstrate flexibility and resilience.
The role involves quality management and design support within the framework of compliance with ISO13485/MDR QMS system.
A competitive salary package is available, although specific figures are not mentioned, and relevant experience is required.

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

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