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If you think you are the right match for the following opportunity, apply after reading the complete description. Director of Quality Assurance The Director of Quality Assurance leads and oversees all QA programs to ensure compliance with FDA regulations for drug products. Responsibilities include managing QA teams, supervising release of materials and products, maintaining the Quality Management System, and ensuring adherence to cGMP standards. This role involves developing SOPs, conducting audits, managing change control, investigating deviations, and acting as the primary liaison during client and regulatory audits. Key Duties: Lead and manage the QA team including hiring and training. Oversee daily QA operations and Quality Management System. Develop and maintain SOPs and inspection standards. Administer auditing and cGMP training programs. Manage change control and review manufacturing and testing procedures. Investigate production discrepancies and ensure quality controls. Participate in meetings, manage QA budget, and handle personnel decisions. Qualifications: Bachelor’s degree in Science (Chemistry, Biology, Pharmacy, or related field). 5+ years of managerial QA experience, preferably in pharmaceuticals. Strong knowledge of cGMP and QA functions. Excellent communication and problem-solving skills. Ability to handle confidential information. Details: Full-time, Monday to Friday, 8-hour shifts. Benefits include health, dental, vision, life insurance, 401(k), and paid time off. On-site work required.