On-site GCP Quality Assurance Auditor

A biopharmaceutical company is seeking a GCP Quality Assurance Auditor to ensure GXP compliance with regulatory authorities. This position requires 5+ years of pharmaceutical experience and intensive GCP knowledge. Responsibilities include conducting global clinical audits and managing non-conformances. The role is on-site in Paramus, NJ. The ideal candidate will have strong Quality Assurance experience and the ability to collaborate with global clinical teams, along with a BS degree in a relevant field. #J-18808-Ljbffr