Site Quality Head will be responsible for leading all quality assurance (QA) and quality control (QC), and quality management system (QMS) activities at the site, ensuring compliance with pharmaceutical industry regulations and the company's internal standards.
This role is crucial in maintaining the safety, efficacy, and regulatory compliance of manufactured products while fostering a quality-driven environment that promotes continuous improvement.
Your Role
Oversee QA and QC operations to ensure all products meet established quality standards.
Implement and maintain the Quality Management System (QMS) in accordance with GMP (Good Manufacturing Practices), ISO, FDA, ANVISA, and other local and international regulations, and company standards.
Ensure ongoing compliance with all relevant pharmaceutical industry regulations and guidelines.
Lead internal and external audits, and manage responses to regulatory inspections.
Develop and implement quality polici...