Medical Devices QMS Auditor

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Location: South Korea (home based)

Duties

• 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

• BSI (British Standards Institution) is the global business standards company that equips busi...