Quality Auditor ISO 13485
Responsibilities :-- The main responsibilities will be to performing the audit at the manufacturing sites of our clients' suppliers per Pro QC checklists.
- Using the process audit to identify relevant risks and point out potential issues.
- Looking at audit findings and classifying them against the ISO 13485 requirements.
- Communicate findings with the audit team and issue audit report within due day.
Qualifications
- ISO 13485 certified or trained
- Require a manufacturing and operations background and medical device expertise
- 2–4+ years in quality management or medical device industry
- Experience with QMS processes (CAPA, validation, design controls, etc.).
Job Type: 1099 Contractor
Project Duration: CURRENT PROJECT: 2-4 days
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Note: This is a 1099 contract role – project duration may vary based on client needs
Shift Hours: CURRENT PROJECT: 8 hours a day.
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Note: As a 1099 contractor, project schedules may vary depending on site availability
Location: Must be able to travel to Twinsburg, OH and nearby areas
(exact CLIENT address can ONLY be shared once contractor is confirmed)
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