CAPA/ Complaints Technical Writer

The CAPA / Complaints Technical Writer is responsible for authoring, reviewing, and maintaining high-quality documentation associated with Corrective and Preventive Actions (CAPA), customer complaints, investigations, non conformances, and Quality Management System (QMS) remediation activities within a regulated medical device environment.

This role ensures that all documentation is scientifically sound, technically accurate, inspection-ready, and compliant with applicable regulatory requirements. The Technical Writer partners with cross-functional teams to support timely closure of quality records while developing clear, concise, and compliant investigation reports, root cause analyses, effectiveness checks, and remediation documentation.

Responsibilities:

• Author and maintain CAPA, complaint, investigation, and remediation documentation.
• Draft root cause analyses, corrective action plans, effectiveness checks, and investigation reports.
• Collaborate with Quality, Engineering, Regulatory Affairs, and Operations teams to document investigation outcomes.
• Ensure compliance with FDA QMSR/21 CFR Part 820, ISO 13485, ISO 14971, MDSAP, and EU MDR requirements.
• Support quality system remediation projects, audits, and regulatory inspections.
• Standardize documentation practices and support continuous improvement initiatives.