Quality Assurance Auditor II - GLP Compliance & Audits

Inotiv in Rockville, MD is seeking a Quality Assurance Auditor II with a B.S. in chemistry or life sciences and 2–4 years in GLP environments, including auditing experience. The role requires strong regulatory knowledge, precise documentation, and the ability to work with cross-functional teams. Responsibilities include conducting audits, preparing reports, maintaining SOPs, and ensuring compliance with FDA and EPA GLPs and international standards.