Associate Director, Head SHE On-Site China

Job description

南通，中国 | 全职 | Job ID: 11660 About the role: As China SHE Associate Director, you will play a key role in the safety, health and environment for employees and company by supporting SS&E head on operation and overseeing the execution of safety operations across region of China. You will be major contact person in China to Global SHE team and receiving global standard/guidelines and will work closely with the local teams in each site to localize global standard in each site and maintain consistently high SHE standards at all sites in China. 作为中国区现场SHE负责人，您将在保障员工和公司安全、健康与环境方面发挥关键作用，协助运营副总裁开展工作，并监督在中国各地区安全、健康与环境运营的执行情况。您将作为中国区和全球总部SHE团队的主要对接人并接受全球标准/指南，并将与各地团队密切合作，确保中国区始终维持高标准的SHE标准以及全球标准在各个现场适当地本地化和执行。. Your contribution: Provide guidance to ensure the effective implementation, integration and continuous improvement of BioNTech’s Global SHE Standards across all sites of China. This includes both strategic oversight and hands-on operational execution working under the guidance of China regional site leadership to maintain a unified, compliant and operationally effective SHE framework. 提供指导以确保百欧恩泰总部SHE标准在中国区的有效实施、整合以及持续改进。这包括战略层面的监督以及在中国区领导层的指导下进行实际操作执行，以维持统一、合规且具有有效运营性的SHE框架。 Counterpart to global SHE team, receive and localize global SHE policy / procedure to China, build up and update SHE operation dashboard with global team 作为全球SHE团队的对接窗口，接受全球SHE政策/规程并本地化至中国区，设立SHE运营仪表盘并更新SHE运营状况 Assist the department head in developing the annual performance targets for SHE in China based on the global SHE annual performance goals, and break them down to each site, monitoring the completion status of the annual performance targets. 协助部门责任人，根据全球SHE年度绩效目标制定中国区的SHE年度绩效，并分解至各个现场，监督年度绩效的完成状态 Oversee and actively manage the governance and performance of third‑party SHE providers, ensuring alignment with BioNTech's standards, contract expectations and long‑range capability requirements across all China sites. 监督并积极管理第三方SHE服务提供商的治理和绩效情况，确保其符合百欧恩泰的标准、合同要求以及在中国区的长期能力需求。 Assess and track risks, drive mitigation, monitor developments and steer incident response and investigations. 评估并跟踪风险，推动风险的降低，监控事态发展，并指导事件响应及调查工作。 Design and manage integrated SHE concepts, technologies and preparedness, ensuring effective, robust protection. 设计并管理综合的SHE理念、技术及准备措施，确保实现高效、稳固的防护。 Serve as the local SHE advisor, offering strategic counsel to executive leadership and business functions and ensuring that China business and SHE priorities are reflected in planning and decision‑making. 担任当地SHE顾问，为高层领导和业务部门提供战略建议，并确保中国的业务和SHE方面的重点能够体现在规划和决策过程中。 Foster a proactive SHE culture across the China network, ensuring that SHE awareness, confidentiality and risk‑informed decision‑making are embedded into China site operations and employee behavior. 在中国范围内培养积极主动的SHE文化，确保SHE意识、保密性以及基于风险的决策制定能够融入中国区的运营以及员工的日常行为之中。 Willingness to travel occasionally, both national and international 愿意接受国内和海外出差。 A good match: Degree in Pharmaceutical / Chemistry Industry / Engineering Management. 具备医药/化工/工程管理专业学士学位 Fluent in English. 英语口语书写熟练 15 years or above SHE related management and compliance experience. 15 年以上SHE相关的管理和合规经验 Understanding of key regulatory authorities for pharmaceuticals, medical devices and therapeutic goods (e.g. NMPA). 对药品、医疗器械及治疗性产品等关键监管机构（如国家药品监督管理局）的了解 On-Site SHE operations: Led SHE strategy establishment and continuous improvement in manufacturing, R&D and employee’s SHE management system, ensuring compliance with global SHE requirement, related laws and corporate policies. Drive each site to establish the effect risk management, accident prevention and emergency response process. 现场SHE运营：负责生产基地、研发以及员工SHE管理体系的建立与持续改进，确保符合全球SHE要求、法律法规及公司政策要求。推动各站点建立有效的风险管理、事故预防和应急响应流程。 SHE vendor management: Managed licensed guarding providers and SHE integrators; set KPIs/SLAs, ran performance reviews and enforced corrective actions. SHE供应商管理：管理有资质的SHE服务提供商；设定关键绩效指标/服务级别协议，进行绩效评估并强制执行纠正措施。 Incident & Investigations: Conducted fact‑finding, evidence collection, and root‑cause analysis; produced investigation reports, CAPA actions and management updates. 事件与调查：进行事实调查、证据收集以及根本原因分析；编制调查报告、纠正预防措施方案以及管理更新内容。 Regulatory/GxP compliance: Operated within GMP‑regulated sites; aligned SHE controls with facility segregation, documentation, and audit readiness expectations; supported inspections and audits. 法规/良好生产规范合规性：在符合 GMP 标准的场所内运营；将SHE控制措施与设施分区、文件记录以及审计准备要求相匹配；为检查和审计工作提供支持。 Green Operation Management: Drive FM zero carbon projects, promoting sustainable development and green operations. 绿色运营管理：推动设施管理零碳项目，促进可持续发展与绿色运营。 China regulatory & compliance context: Applied knowledge of NMPA‑governed pharmaceutical production and facility controls; operated within PIPL/data‑protection requirements; adhered to China anti‑corruption/compliance standards for pharma/med‑device. 中国监管与合规背景：具备国家药品监督管理局（NMPA）监管下的药品生产及设施控制方面的专业知识；遵守《个人信息保护法》/数据保护要求；遵循中国针对制药/医疗器械的反腐败/合规标准。 SHE On-site Center build‑out: Planned and stood up a SHE operation center, covering technical architecture, SOPs, staffing, shift design and runbooks. 现场SHE建设：规划并搭建安全控制室/安全运营中心，涵盖技术架构、标准操作流程、人员配置、轮班安排以及操作手册等方面。 Regional SHE Operations: Oversee China Regional SHE Operations Center operations, including third‑party management and technical/operational integration with sites and the Global SHE Operation Center. 区域SHE运营：监督中国区SHE运营中心的运作情况，包括第三方管理以及与各站点及全球SHE运营中心的技术和运营整合工作。 BioNTech 重视每一位团队成员的福祉，为多元化的员工提供全面的福利保障。我们提供具有市场竞争力的薪酬方案，具体将根据职位、工作地点及候选人资历与经验综合确定。注：各项福利的实际适用范围、享有条件及具体内容可能因所在地而异，最终以公司内部政策及当地法律法规为准。 申请方式： 请通过我们的在线申请链接提交以下材料： 个人简历 学位证书及职业资格证书复印件 联系方式 重要提示： 我们仅接受通过链接在线提交的求职申请。 提交申请即视为您知悉，招聘流程中将依相关法律法规进行背景调查。如您进入候选名单，BioNTech 将通过合作服务机构“HireRight”开展背景调查工作，招聘专员将及时与您沟通具体安排。 我们诚挚期待您的加入。