Anonymous Company
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
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