GLP QA Auditor I - Compliance & Risk Champion

INTEGRATED LABORATORY SYSTEMS LLC

Durham (NC)

On-site

USD 70,000 - 110,000

Full time

14 days+

Application generator

Turn this role into an interview — a resume and cover letter built around what this employer wants.

Get past ATS filters

Job summary

Inotiv in Durham, NC is seeking a QA Auditor to support GLP compliance across designated studies and facilities. You will conduct audits, review study protocols and data, and prepare formal audit reports for Study Director and management.

The role requires 2–4 years in GLP or regulated environments, strong regulatory knowledge, and excellent communication. Work is performed in an office/lab setting with opportunities for growth in QA leadership.

Qualifications

B.S. in chemistry or life sciences or related field; 2-4 years in a GLP-enabled environment.
One or more years of auditing experience in a regulatory/quality setting.
Excellent written and verbal communication; ability to interact with all levels of the organization.
Strong organizational skills and attention to detail.
Proficient with Word, Outlook, Excel, SharePoint.

Responsibilities

Conduct audits of designated studies and facilities to assess protocol compliance.
Prepare audit reports and promptly submit findings to Study Director/PI and management.
Stay current on FDA/EPA GLPs and applicable regulations.
Perform QA duties and assist in training for new hires.
Assist with subcontractor and vendor evaluations.