Medical devices QMS ISO13485 auditor

Overview

Position : Medical devices assessor

Location : South Korea (home based)

Responsibilities

• As a RS Client Manager (Assessor) you'll be responsible for frequently travelling and having overnight stays across South Korea. You'll assess to ISO 13485 quality management systems, EU medical device regulations and MDSAP scheme on customer sites, write up comprehensive reports and present these to the client. You'll also have the opportunity for occasional international travel to the USA and Europe.
• You'll undertake extensive training to deliver in your role. This includes : ISO13485 Lead Auditor course, MDSAP (Medical Device Single Audit Programme), and MDR (Medical Device Regulation).

About BSI and the Regulatory Services Team

Key responsibilities & accountabilities

Candidate specifications

Key performance indicators

Our Excellence Behaviours

Client-centric, Agile, Collaborative. These three behaviours represent how we do things at BSI. They help us ensure that BSI is a great place to work and a highly successful business.

BSI is conducting face-to-face interviews where appropriate and possible. If you are invited to a face-to-face interview but feel more comfortable with conducting the interview virtually, please speak to a member of our recruitment team.

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