Job Description: Mastery of Quality Management Systems (QMS), GMP and GDP Mastery of Deviation, CAPA, Change Control, Risk Assessment and Complaint Handling Mastery of SOP and protocol documentation and writing Familiarity with the principles of Quality Risk Management (QRM) Mastery of document management systems, continuous improvement and analysis of quality indicators, implementation of quality improvement projects and submission of periodic reports to the organization's senior management Supervision and control of SMF, VMP, CTD, DMF documentation Supervision, monitoring and review of production information and product quality control Participation in the validation of water and air conditioning systems in various production departments and clean rooms Ability to plan and implement internal and external audits Compile, review and control documentation, implementation methods and quality guidelines Eligibility requirements: At least 8 years of experience in quality assurance management in the pharmaceutical and supplement industries Leadership and team management skills Decision-making and problem-solving abilities Communication and negotiation skills Effective English proficiency