Auditor

• Responsible for assessing ISO 13485 quality management systems, EU medical device regulations, and MDSAP scheme on customer sites
• Write comprehensive reports and present to clients
• Undertake management system assessments in accordance with BSI requirements
• Prepare assessment reports and deliver findings to clients
• Recommend the issue, re-issue or withdrawal of certificates
• Lead assessment teams ensuring effective working relationships with clients and team members
• Develop client partnerships to enhance business opportunities
• Provide accurate and prompt information to support services
• Plan/schedule workloads to maximize revenue-earning activity
• Coach colleagues and assist in their induction

Medical Devices QMS ISO 13485 Auditor