Quality Assurance Auditor I — GLP Compliance & Audits

INTEGRATED LABORATORY SYSTEMS LLC; North Carolina; On-site; USD 65,000 - 95,000; Full time

Benefits offered by this job

Health and dental coverage

Job summary

Inotiv in North Carolina is seeking a QA Auditor to support GLP compliance across studies and facilities. You will audit study conduct, review protocols, and help ensure accurate data and reporting.

The role requires a B.S. in a scientific field and 2–4 years in regulated environments, with auditing experience preferred. You will follow SOPs, use QA software, and collaborate with sponsors and regulatory agencies.

Qualifications

• Bachelor's degree or higher in chemistry, life sciences, or related field with GLP experience.
• 2–4 years in a regulated environment, ideally with auditing experience.
• Equivalent mix of education and regulatory/quality/compliance experience.

Responsibilities

• Follow SOPs and ensure compliance with study protocols and policies.
• Prepare audit reports and communicate findings to management.
• Conduct audits of studies and facilities for protocol compliance.
• Maintain knowledge of FDA and EPA GLPs and related regulations.

Skills

Written communication

Verbal communication

Interpersonal skills

Organizational skills

Lab procedures

Regulatory knowledge

Independent work

QA software

Auditing experience

Root cause analysis

Education

Bachelor's degree in related field

Job description

Inotiv in North Carolina is seeking a QA Auditor to support GLP compliance across studies and facilities. You will audit study conduct, review protocols, and help ensure accurate data and reporting.

The role requires a B.S. in a scientific field and 2–4 years in regulated environments, with auditing experience preferred. You will follow SOPs, use QA software, and collaborate with sponsors and regulatory agencies.