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Quality Systems & Regulatory Compliance Manager

twonice · Waterbury, Connecticut, United States

External listingfull-timeRecently

About The Role

**Quality Systems & Regulatory Compliance Manager**

**Location: near Waterbury, CT**

**Salary: $90,000–$120,000 + Annual Bonus Potential + Benefits**

**Benefits: Medical, Dental, Vision, 401(k) w/ match, Holidays, PTO**

**Job Type: Full-Time | On-site**

**Typical Hours: Monday–Friday, 40 hours/week**

**Start Date: ASAP**

**Sponsorship is not available**

**Relocation assistance available**

**Quality Systems & Regulatory Compliance Manager Description**

Our client in precision manufacturing is looking for a Quality Systems & Regulatory Compliance Manager to join its team near Waterbury, CT. You will own regulatory compliance and audit coordination, while partnering with a Quality Engineer to resolve customer complaints, conduct root-cause analysis and drive corrective and preventative actions. This role requires experience owning ISO 13485 compliance in a precision-manufacturing environment and audit participation. You must also understand FDA requirements, CAPA, and customer quality processes. This is a great opportunity to learn from the current leader during a planned transition before taking full ownership of the function at a financially strong manufacturer, investing in new technology, employee development, and long-term growth.

**Quality Systems & Regulatory Compliance Manager Responsibilities**

  • Own regulatory and quality-system compliance programs
  • Maintain regulatory filings, certifications, and supporting records
  • Monitor FDA, ISO 13485, QMSR, ITAR, and EAR requirements
  • Coordinate customer complaints, root-cause analysis, and CAPAs
  • Lead customer audits and verify timely closure of findings
  • Manage internal audits, auditor training, and corrective actions
  • Track complaint trends, audit findings, PPM, and customer quality metrics
  • Escalate compliance risks and stop processes that violate requirements
  • Support customer quality agreements and document-control processes
  • Train teams on regulatory, audit, and documentation requirements

**Quality Systems & Regulatory Compliance Manager Qualifications**

  • 7+ years of regulatory compliance or quality-system ownership experience required
  • ISO 13485 and FDA QMSR/21 CFR Part 820 compliance experience required
  • Customer complaints, CAPA, root-cause analysis, and audit experience required
  • Working knowledge of ITAR/EAR and environmental compliance required
  • Microsoft Office proficiency required

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