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 >Note: This is a 1099 contract role – project duration may vary based on client needs

Shift Hours: CURRENT PROJECT: 8 hours a day. >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)