The MS&T Process Senior Scientist provides technical support to the Self Care China manufacturing operations group, including formula and process support, technical projects, investigations and validation execution. The role partners with the global MS&T CoE’s, the regional MS&T team and with internal Manufacturing management and Quality Assurance partners in the region to identify, prioritize, and execute technical projects including technology transfers, process capability improvements, and compliance remediations impacting cost, compliance, validation activities and customer service. The role also assumes responsibility for executing solids and liquids projects with the SJJP site and China EM’s. The position has direct responsibility for collaboration of technical and functional resources to drive continuous improvement and consistency in tech transfer and manufacture of solid and liquid dose OTC products/processes. ·Ensure quality and compliance in all actions: o Attend GMP training on the schedule designated for role and as appropriate for role. o Adhere to strict compliance with procedures applicable to role. o Exercise the highest level of integrity in the tasks performed. o In a timely and prompt manner, identify, report and seek correction for deviations noted in the workplace. o Embrace a behavior of employee involvement and commitment to doing the job right the first time. o Ensuring employees under the position’s scope of responsibility are trained in required procedures for the execution of their role and maintain current with training requirements during the year. o Promoting an environment of employee engagement in the workplace. o Seeking prompt identification, reporting and correction of deviations in the workplace as noted by employees. · Execute technical projects in accordance with the company policies and procedures · Provide support to the in progress key projects which impacting revenue growth, quality improvements, compliance remediation, and cost reduction. Effectively collaborate with cross-functional team to optimize business results. Provide support to resolve issues impacting timely completion and achievement of project goals. · Partners with the Validation CoE to execute site Process and Cleaning Validation activities · Partners to deliver and execute key projects according to critical processes including, but not limited to, Tech Transfer, Characterization, Validation and EM site Hyper care. · Support effective product lifecycle and knowledge management in close collaboration with the Regional and Global MS&T and technical need state leaders. · Partner with Research and Development to establish and maintain processes for planning, developing, and commercializing new products resulting in well-characterized, validated, highly capable, cost effective manufacturing processes.

教育背景：本科及以上学历。工作经验：在制药企业技术部门（非研发岗）拥有至少 5 年工作经验（8 年者优先）。岗位名称：技术工程师或验证工程师。专业知识：深入理解 GMP（药品生产质量管理规范），且必须具备工艺验证与清洁验证的相关经验。软技能：具备出色的沟通能力。其他要求：简历中最好附上照片