Senior GCP QA Auditor — On-Site in NJ

A biopharmaceutical company in Northern New Jersey is seeking a GCP Quality Assurance Sr. Auditor. Candidates should have 5+ years of experience in the pharmaceutical industry, with a strong background in GCP and safety, especially with Radiopharmaceuticals. This on-site position involves planning and conducting audits for clinical processes and vendors, ensuring compliance with regulatory standards, and supporting quality management initiatives. The role also requires strong collaboration with global clinical teams and occasional travel. #J-18808-Ljbffr