Job Description
Qualifications
- Bachelor’s degree (science or related field)
- 6 months–2 years of experience in quality, compliance, or regulated manufacturing
- Experience with document control, record control, and CAPA systems
- Familiarity with regulated quality systems (ISO 13485, FDA, Health Canada, or EU MDR)
- Strong working knowledge of Microsoft Office (Word, Excel)
Preferred Skills
- Lead Auditor certification or internal audit experience
- Experience supporting regulatory submissions or Regulatory Affairs
- Medical device or IVD industry background
Day-to-Day Responsibilities
Insight Global is looking to hire a Quality Compliance Associate to support quality system compliance activities within a regulated manufacturing environment. This individual will perform internal audits, prepare audit reports, complete...