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 effectiveness checks, and support audit closures. They will review and approve quality system records including deviations, CAPAs, ICARs, and effectiveness checks, while also assisting supervisors with investigations and corrective actions. The role includes document and record control responsibilities, preparing weekly CAPA metrics and document control metrics, and supporting site change control and supplier management processes. The associate will help maintain SOPs and quality documentation, participate in global compliance initiatives, and support periodic reviews of regulatory standards and gap assessments. This role works cross-functionally with manufacturing, quality, customer service, and shipping teams. Compensation $19to $22. Exact compensation may vary based on several factors, including skills, experience, and education. Benefits Benefit packages for this role will start on the 1st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law. #J-18808-Ljbffr