保存工作 返回搜索结果 职责描述 职位概要 类似职位 Join a new green field project due to business growing. Very good company culture and global well-known platform. 关于我们的客户 Client is a global well-knonw pharmaceutical company with manufacturing site in China for long history. Now expanding new plant due to business growing. 职责描述 1. Oversee and control production conditions, environment, sanitation, and facilities to ensure compliance with GMP/ISO standards. Ensure all processes and procedures are followed, guaranteeing the release of high-quality products to the next phase of production. 2. Lead process improvement initiatives and optimize material utilization, ensuring the validation of production processes, equipment, and cleaning procedures. 3. Organize investigations and analysis of deviations and complaints; ensure effective implementation of CAPA actions related to production activities. 4. Develop and implement necessary Standard Operating Procedures (SOPs) and continuously drive improvements to ensure high-quality standards are met. 5. Oversee the manufacturing and storage of pharmaceutical products in accordance with approved procedures to ensure product quality. 6. Ensure that all manufacturing procedures are strictly followed throughout the production process. 7. Ensure batch production records (including batch packaging records, CCP, and OPRP confirmation records) are properly audited, signed off by designated personnel, and submitted to the quality management department. 8. Oversee CIP (Clean-In-Place) & production process HACCP analysis, including FSHCP data collection (flowchart, process description, product description, etc.). Ensure proper implementation, operator training, and on-site visual management. 9. Collaborate with the maintenance team to ensure effective maintenance of the workshop and equipment, ensuring optimal working conditions. 10. Ensure all manufacturing personnel receive appropriate pre-job and on-the-job training, adjusting training content based on evolving operational needs. 理想的求职者 * Bachelor's degree in Pharmaceutical Engineering, Chemical Engineering, or related field. * Minimum of 8 years of production management experience, with at least 3 years in the pharmaceutical or related industry (experience in liquid pharmaceutical manufacturing is a plus). * Strong understanding of GMP/ISO standards, production processes, and quality management systems. * Experience in designing and managing automated production lines, equipment validation, and process optimization. * Familiarity with MES (Manufacturing Execution Systems) deployment is preferred. * Excellent problem-solving, leadership, and communication skills. * Fluency in both Chinese and English is required. 薪酬待遇 Competitive salary package. 联系 Chris Qu 职位编号 JN-022025-6669585 联系电话 +86 21 6035 3502 职位概要 职位类别 工程与制造 子类别 生产/制造 行业 医疗保健/制药 地区 无锡市 工作类型 全职 顾问名字 Chris Qu 顾问电话号码 +86 21 6035 3502 职位编号 JN-022025-6669585