Mid-Senior QA Specialist — Sterile Pharma

A leading staffing solutions company is seeking a Quality Assurance Specialist for their team in Charleston, SC. This role involves ensuring compliance with cGMP standards in a sterile manufacturing environment. Candidates should have a bachelor's degree in a related field, with 3+ years of experience in GMP-regulated environments. Responsibilities include auditing, quality documentation, and supporting regulatory audits. A comprehensive benefits package is offered, including relocation assistance. #J-18808-Ljbffr