Primary Responsibilities QUALITY AUDITORS:

Seeking ISO 13485 Auditor with European MDR, but only for Class 1 Medical Devices

Provides timely, detailed reports and photographic evidence.

Certifications Requirements:

Certification ISO 13485 Auditor

Experience Requirements:

Medical Industry Experience

Must be able to use MS Word and Excel to submit documents and reports within the time specified (usually within 24 hours after job completion)

Ability to work well in independent and group problem-solving situations

Ability to maintain a positive, professional disposition when adapting to occasional disruptions and unexpected events

Flexibility in scheduling

Job Type: 1099 Contract

Benefits: Flexible schedule

Experience level: 5 years

Work setting: In-person

License/Certification: ISO 13485 Auditor (Preferred)