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
