GCP Auditor SOP Writer

Job Summary

A company is looking for a GCP Auditor and SOP Technical Writer, QA Compliance Consultant based in the US.

Key Responsibilities:

• Represent the company in quality assurance and regulatory/GxP areas
• Provide consultation and manage projects within the Clinical CQA business practice
• Support the implementation and promotion of the company’s CQA program in compliance with GCP regulations

Required Qualifications:

• Experience in quality assurance and regulatory/GxP compliance projects
• Knowledge of GxP auditing, SOP writing/revisions, and Quality Management Systems
• Training in Clinical CQA, including QMS Development, QA oversight, and regulatory agency action response
• Experience in promoting CQA services through social media content and blogs
• Ability to provide CQA-specific training to clients and associates within other business units