Site QA Engineer

Main Responsibilities: • Conduct on-site inspections of production workshops and warehouses to ensure compliance with GMP and relevant quality standards • Review and approve the release of raw materials, ensuring they meet quality requirements before use • Review and approve the release of packaging materials, ensuring compliance with specifications • Manage and issue cleaning records, ensuring traceability of the cleaning process • Review master cleaning records to ensure compliance and effectiveness of cleaning procedures • Handle cleaning deviations, coordinate with relevant departments for investigation and implementation of corrective actions • Review cleaning impact assessments to evaluate the potential impact of cleaning deviations on product quality • Participate in continuous improvement of the quality management system and promote on-site quality management • Maintain effective communication with production, warehouse, and quality-related departments to ensure smooth information flow Qualifications: • Bachelor’s degree or above, preferably in Pharmacy, Chemistry, Quality Management, or related fields • 1-3 years of experience in QA or production in the pharmaceutical industry，familiar with GMP and related regulatory requirements.Fresh graduate are welcome. • Proficient in on-site quality management processes; capable of working communication in both Chinese and English • Strong communication and coordination skills with a team-oriented mindset • Detail-oriented, responsible, with strong problem-solving and analytical abilities