Perform visual, dimensional, and functional inspections of medical device components, subassemblies, and finished products.
Ensure products meet quality standards, engineering specifications, and regulatory requirements.
Inspect parts using blueprints, drawings, inspection guides, and precision measuring equipment.
Conduct incoming, in-process, and final inspections to verify product conformity.
Perform First Article Inspections (FAI) and verify inspection data when required.
Review Device History Records (DHRs) and quality documentation for accuracy and compliance.
Process inspection results, product release activities, and quality transactions within the ERP system.
Identify, document, and quarantine nonconforming materials while initiating nonconformance reports as needed.
Maintain compliance with Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and company quality procedures.
Support departmental quality, productivity, and Key Performance Indicator (KPI) goals.
Maintain accurate inspection records and documentation to ensure product traceability.
Work collaboratively with Manufacturing, Engineering, and Quality teams to resolve quality issues and support continuous improvement initiatives.
Follow established procedures and work instructions while maintaining a safe and organized work environment.
This is an entry-level opportunity with training provided for candidates looking to build a career in Quality Assurance and Medical Device Manufacturing.
| Location | Weston, Florida |
| Job Type | Temporary |
| Industry | Staffing/Employment Agencies |
| Salary | $20 Per Hour |
| Company Size | 2,500 to 4,999 employees |
| Website | https://www.roseint.com/ |
Founded in 1993 by Sue Bhatia, Rose International is one of the nation's leading minority- and woman-owned providers of Staffing and Total Talent Solutions. We serve companies in all 50 states and employ thousands of people across the country.
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