Quality Assurance Director – Commercial cGMP Manufacturing On site, MA API and Generic cGMP Manufacturing We are seeking an experienced Quality Assurance Director to lead QA operations in commercial cGMP manufacturing. With over 35 years of expertise, we specialize in providing high-quality contract development and manufacturing services to the global pharmaceutical industry. Role Overview: You will oversee all QA activities related to commercial cGMP manufacturing, ensuring compliance with FDA, EMA, and other regulatory standards. Your leadership will drive continuous improvement, regulatory inspections, and quality management across the organization. Key Responsibilities: Lead and manage QA activities in cGMP manufacturing. Ensure compliance with global regulatory standards. Oversee batch release, investigations, and CAPA. Mentor and develop the QA team. Qualifications: 10+ years in QA in a commercial cGMP manufacturing environment, with 5+ years in leadership. Strong knowledge of FDA, EMA, and global cGMP regulations. Leadership, communication, and problem-solving skills. Why Join Us? Competitive salary and benefits. Growth opportunities in a leading organization. Be part of a dynamic, innovative team . Apply today to advance your career in a trusted, globally recognized company. #J-18808-Ljbffr RBW Consulting
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