Associate QA Director

Associate QA Director

About the role

百欧恩泰（珠海） MAH质量保证（QA）负责人是一个领导岗位，负责监管本公司及其CDMO（合同开发与生产组织）的所有质量保证活动。该负责人将确保生物制品的生产、检测、放行及分销环节均符合监管要求、行业标准以及BioNTech内部的各项政策、标准和标准操作规程（SOP）。此外，该负责人将建立和提升百欧恩泰（珠海） MAH质量管理体系（QMS）包括监管CDMO相关活动，对CDMO实施质量监督，推动持续改进举措，与跨职能团队协作，并确保产品质量与患者安全达到高标准。该岗位负责产品放行给临床试验和商业化市场

The QA Head for BioNTech-Zhuhai MAH is a leadership role responsible for the quality assurance of the drug products manufactured by BioNTech subsidiaries or CDMOs. The incumbent will ensure quality compliance with China regulatory requirements, industry standards, and BioNTech internal policies, standards, and SOPs for the manufacturing, testing, release and distribution of biological products (clinical and commercial). The incumbent will establish and improve the BioNTech MAH QMS for the assurance of drug products and oversight of the CDMO activities and drive continuous improvement initiatives, work with cross-functional teams, and ensure the highest standards of product quality and patient safety. The incumbent will be responsible for drug product release for both clinical trials and commercial markets.

Your contribution:

• 负责MAH质量体系的建立和完善，确保其有效运作，制定质量战略目标及年度工作重点，管理百欧恩泰珠海（MAH）公司质量运营工作 Set up effective MAH quality systems and continuously improve them; develop annual strategic quality goals; and lead quality operations of BioNTech (Zhuhai)
• 负责国内药监机构GMP检查工作; 协助检查组开展现场检查，负责检查发现项回复, 整改工作进行，确保各项发现项的整改工作按时完成 Oversee all GMP inspections by Chinese regulatory agencies and assist inspectors to perform effective inspections, lead inspection response to the inspection findings/observations if any, development of CAPA for the inspection findings, and ensure the timely completion of the CAPAs related regulatory inspection findings/observations
• 审核偏差和检验结果超标的处理报告，跟踪产品质量问题，分析质量偏差的根本原因，并提出方案确保偏差等问题得到及时处理 Review and approve the deviations, OOS, complaints and change controls; follow up critical product quality related issues; review root cause analysis trends for quality deviations and the effectiveness of implemented CAPAs, other key quality performance metrics
• 审核产品的工艺规程、质量标准、取样方法、检测方法和其他质量管理的操作规程、以及与质量有关的所有的变更 Review manufacturing process procedures, specifications, sampling methods, testing methods and other quality management SOPs, as well as all quality-related changes
• 审核工艺验证方案和报告，确保各项必要的验证工作得到及时完成 Review process validation protocols and reports, ensure all the necessary verifications and validation are completed in time
• 承担产品放行的职责，确保每批产品放行前，完成所