Quality Assurance Auditor I - GLP Compliance

Inotiv; Morrisville (NC); On-site; USD 70,000 - 95,000; Full time

Job summary

Inotiv in Morrisville, NC is seeking a QA Auditor with a B.S. in chemistry or life sciences and 2–4 years in GLP environments to join our QA team.

You will conduct audits of studies and facilities, prepare audit reports, and help ensure compliance with FDA, EPA GLP, and relevant regulations.

This role offers exposure to corrective actions, training, and collaboration with sponsors, driving quality improvements within a leading CRO. Salary will be commensurate with experience.

Qualifications

• B.S. in chemistry or life sciences or related field.
• 2–4 years in a GLP or regulated environment, preferably with auditing.
• Equivalent mix of education and regulatory/quality experience.

Responsibilities

• Conduct audits of studies and facilities for regulatory compliance.
• Prepare audit reports and communicate findings to management.
• Assist with SOP adherence, training, and regulatory projects.
• Interact with sponsors and regulatory bodies as needed.

Skills

GLP knowledge

Auditing

Regulatory awareness

Written and verbal communication

Interpersonal skills

Organizational skills

Detail oriented

Laboratory procedures awareness

Regulations comprehension

QA tools familiarity

Education

B.S. in chemistry or life sciences or Bachelor’s degree or higher in a related field

Tools

Word

Outlook

Excel

SharePoint

Job description

Inotiv in Morrisville, NC is seeking a QA Auditor with a B.S. in chemistry or life sciences and 2–4 years in GLP environments to join our QA team.

You will conduct audits of studies and facilities, prepare audit reports, and help ensure compliance with FDA, EPA GLP, and relevant regulations.

This role offers exposure to corrective actions, training, and collaboration with sponsors, driving quality improvements within a leading CRO. Salary will be commensurate with experience.