Johnson & Johnson is on FGB’s Best Companies for Women of 2020.
FGB'ers gave this company a 4.3/5 in overall job satisfaction
FGB’ers working at Johnson & Johnson rated their manager’s support a 4.4/5
Global parental leave for all new parents (maternal, paternal, adoptive or surrogacy-assisted).
Global exercise reimbursement.
Two weeks off (one of them fully paid) for volunteer work.
Align with company and commercial strategy, follow team plan, manage and implement project registration activities focused on project execution and delivery. 基于公司和业务策略，根据团队计划，管理和实施项目注册工作，着重于项目执行与交付。 Response for day-to-day operation to ensure registration related projects/programs progress. prepare required information for the registration dossier and technical requirement document. 负责日常运营，以确保注册相关项目/计划的流程妥善实施。完成注册资料和技术要求文件所需信息。 Follow the guidance from the leader team, allocate and use resources properly, and actively cooperate with team in order to achieve goals. 根据管理团队提供的指导，合理配置和利用资源，积极和团队合作从而高质量的完成项目。 Interact and proactively with cross functional partners, including global regulatory functions, quality, R&D, manufacture and commercial partners, make sure projects go smoothly. 与公司跨部门合作伙伴，包括全球法规部门、质量、研发、生产和商业伙伴积极互动。确保项目顺利进行。 Mintain and familiar with the daily work channel with NMPA and other authorities. 熟悉并保持与NMPA以及其他监管部门之间的正常工作渠道。 Provide regulatory support for cross functional departments and cultivate company regulatory compliance environment. 为跨职能部门提供法规支持，并营造公司法规合规运营环境。 Identify, evaluate and interpret new policies and regulations and standard. 发现、评估并解读政策法规和标准等方面的新政策与法规。 Attend policy shaping, standard improvement etc. to support JnJ project and business. 参与制定政策、标准改进等工作，以支持强生项目和业务。 Propose plan & implement improvements to company related procedures improve product registration efficiency and quality. 针对公司相关程序提出计划并实施改进措施，以提高产品注册效率和质量。 Cultivate a collaborative, trusting and ethical working environment that positively contributes to engagement and capability development within RA department and cross functional team. 在法规事务部内和跨职能团队营造合作、互信、有职业道德的工作环境，积极提升个人参与度和能力发展。 Understand and adherence to J&J Credo and value of Credo based decision. Follow and delivery on execution on company and departmental strategy. 了解并遵守强生信条和基于信条价值观的决策。遵守和执行公司和部门战略并交付成果。 According to company requirement and policy, provide self on-going performance management and periodic formal evaluation, improve competency to meet job required capabilities. 根据公司相关要求和政策，进行自我绩效管理并定期进行正式评估。确保掌握工作所需的能力。 Strictly maintain confidential information and intellectual property (IP) includes product development information, designs, manufacture process, trade secrets, government reporting and legal matters, sales volumes and marketing strategies. 严格保守公司机密信息并维护公司知识产权，包括产品研发信息、设计、生产流程、商业机密、政府汇报和法律事宜、销售量和市场策略。 All work will be carried out in accordance with company policies and procedures. Ability to comply with the Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations. 所有工作均须按照公司政策和程序予以开展。能够遵守质量管理体系、质量管理政策、质量目标和相关法律及法规。 Qualifications B.S. in medical, material, mechanical/biomechanical engineering or pharma. An advanced degree (Masters) in above subjects is strongly preferred. MBA and/or PhD is a plus. 拥有医学、材料学、机械/生物机械工程或制药专业学士及以上学位。以上领域高学历（硕士）优先。 More than 5 years RA experience in medical device industry. 在医疗器械行业拥有5年以上法规事务经验。 Familiar with China and oversea regulations (if applicable) of medical device and registration process, familiar with knowledge of product design process, product feature, product test and manufacture process. 熟悉中国和其他国家的医疗器械法规（如适用）和注册流程；熟知产品设计流程、产品特点、产品检测和生产流程相关知识。 Strong organization, planning, coordination and execution ability; keen observation ability, strong comprehensive analysis ability. 拥有较强的组织、计划、协调和执行能力；敏锐的观察力、良好的综合分析能力。 Exhibits excellent time management and project management skills. 展现出良好的时间管理能力和项目管理能力。 Ability to manage and allocate resources to assigned projects which result in completing projects on time and within budget. 能够管理所分配的项目并配置资源，使得项目按时完成且将成本控制在预算之内。 Ability to effectively use negotiation and conflict management skills to ensure delivery of regulatory deliverables. 能够有效使用谈判和冲突管理技能确保法规可交付成果的交付。 Excellent problem solving and demonstrated excellent execution capability. 卓越的问题解决能力和执行力。 Honest, positive, diligent and dedicated, with excellent team spirit and overall vision, highly disciplined, demonstrated high level of initiative. 诚实、积极、勤奋、专注，拥有较强的团队精神和全局观，高度自律，拥有高度的主动性。 Curiosity and passion for new regulation, policy and technologies. 对新的法规、政策和技术充满好奇心和热情。 Fluent in both Mandarin and English. 中英文流利。 Primary Location China-Beijing-Beijing- Organization Johnson & Johnson Medical Shanghai Ltd. (7055) Job Function Regulatory Affairs Requisition ID 2206035596W
Child care benefits
Short term disability