A company is looking for a Quality Assurance (QA) Compliance Specialist III.
Key Responsibilities
Maintain effective liaison with various Client Areas and TPM sites
Ensure production at TPM sites complies with current good manufacturing practices and specifications
Review and approve manufacturing directions and conduct thorough investigations of plant events
Required Qualifications
Bachelor's degree preferably in Engineering or Science
Six years of experience in Pharmaceutical operations, preferably in Biologic manufacturing
Knowledge of GMP regulations and standards affecting pharmaceutical products
Comprehensive knowledge of business and quality concepts
Experience with Change plans, Exception Reports, SAP, and LRMS is preferred
Quality Assurance Specialist • Davie, Florida, United States