QA Auditor I: GLP Compliance & Audits

Inotiv; Northern (KY); Hybrid; USD 70,000 - 95,000; Full time

Benefits offered by this job

Health and dental coverage

401K

Paid time off

Job summary

Inotiv is seeking a QA Auditor to join our QA team in Kentucky. You will support audits of designated studies, review protocols and reports, and ensure compliance with GLP, FDA, EPA, and international regulations. You will prepare audit findings, maintain SOP knowledge, and assist with regulatory projects.

The ideal candidate has a B.S. in chemistry or life sciences and 2–4 years in a GLP or regulated environment, with auditing experience preferred, and strong written and verbal communication

Qualifications

• B.S. in chemistry or life sciences or related field.
• Two to four years of experience in a GLP or similarly regulated environment.
• Auditing experience preferred and regulatory/compliance exposure.

Responsibilities

• Follow SOPs and company policies to ensure QA compliance.
• Conduct audits of designated studies and facilities and report findings.
• Prepare audit reports and assist with regulatory projects.

Skills

Written and verbal communication

Interpersonal skills

Organizational skills

Laboratory procedures knowledge

Regulatory compliance

Audit experience

QA systems knowledge

Problem solving

Data analysis

Education

B.S. in chemistry or life sciences or related field

Tools

Word

Outlook

Excel

SharePoint

Job description

Inotiv is seeking a QA Auditor to join our QA team in Kentucky. You will support audits of designated studies, review protocols and reports, and ensure compliance with GLP, FDA, EPA, and international regulations. You will prepare audit findings, maintain SOP knowledge, and assist with regulatory projects.

The ideal candidate has a B.S. in chemistry or life sciences and 2–4 years in a GLP or regulated environment, with auditing experience preferred, and strong written and verbal communication