QA Auditor I — GLP Compliance & Audit Specialist
Dormont Manufacturing Co
Inotiv is seeking aQuality Assurance Auditor I to perform audits of designated studies and facilities, ensuring adherence to protocols, SOPs, and regulatory requirements. The role involves preparing audit reports, ensuring data integrity, and supporting regulatory guidance within the QA team. The candidate should have relevant education in chemistry or life sciences and 1–3 years of pharmaceutical auditing experience, with strong communication and organizational skills. #J-18808-Ljbffr Dormont Manufacturing Co
Vacancy posted 1 day ago
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