GCP QA Auditor — Clinical Compliance Expert

OLSA Resources, Inc.; United States; On-site; USD 60,000 - 80,000; Full time

Job summary

A Quality Assurance Consulting Firm based in the United States is looking for a dedicated Quality Assurance professional. The ideal candidate will have 2-5 years of related experience, especially in QA auditing within the pharmaceutical industry. Responsibilities include conducting internal and external audits, generating reports, and working closely with various teams. Strong communication and writing skills are critical for this role. This position offers opportunities for professional development in a regulatory environment.

Qualifications

• 2-5 years in Quality Assurance or clinical research organization.
• 1-2 years QA auditing experience, GCP auditing preferred.
• Experience in the pharmaceutical industry required.

Responsibilities

• Conduct internal and external audits of clinical sites and vendors.
• Generate audit reports and quality assurance presentations.
• Assist team during report audits and maintain liaisons with departments.

Skills

Writing skills

Communication skills

Auditing experience

Education

Bachelor's Degree in physical or life science, nursing or pharmacy

Job description

A Quality Assurance Consulting Firm based in the United States is looking for a dedicated Quality Assurance professional. The ideal candidate will have 2-5 years of related experience, especially in QA auditing within the pharmaceutical industry. Responsibilities include conducting internal and external audits, generating reports, and working closely with various teams. Strong communication and writing skills are critical for this role. This position offers opportunities for professional development in a regulatory environment.