Quality Assurance Auditor III

Maintain thorough knowledge of facility SOPs, policies, study protocols, etc. Perform other duties as assigned Issue accurate quality assurance statements for inclusion in final reports

Demonstrate solid knowledge of electronic data collection systems used in data generation, including proper use, reporting, audit trails, security/Part 11 compliance, data correction, and QC Actively participate in managing quality program to ensure compliance with regulatory requirements and serve as a resource for staff on regulatory topics. in quality assurance inspections from existing or potential clients and regulatory agencies. Perform other duties as assigned.

* Education and Experience
* Three to five years of experience in a GLP preferably with 1-3 or more years of auditing experience, or Equivalent combination of education and regulatory, quality, compliance and/or industry experience.### Get In Touch Introduce yourself to our recruiters and we'll get in touch if there's a role that seems like a good match.

We’re looking for people who will help us grow and support our shared purpose: to help our clients discover and develop life-changing therapies for people around the world.  As a leading contract research organization (CRO), Inotiv supports discovery and nonclinical development through investigational new drug (IND) and beyond. By leveraging our deep expertise and scientific capabilities, we help you increase efficiency, improve data, and reduce the cost of taking new drugs to market.

By providing critical research models and related services, we help researchers realize the full potential of their R&D projects, all while working together to build a healthier and safer world.  We hope you consider our opportunities and a future with Inotiv!
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