北京招聘

供应商管理 Supplier Quality Management:

1. 遵循中国本地法规、强生全球/亚太地区的政策及适用的行业标准，通过有计划的审核及不定期的访问、联络、跟踪改进等形式，确保供应商的质量管理体系及相关作业规程能始终达成高度的符合性和有效性，满足强生公司及产品的要求。包括新的及现有供应商。
Ensure high level of compliance and effectiveness of suppliers’ quality management system and pertinent processes so as to comply with local China regulations, J&J corporate / regional policies / guidance and applicable industrial standards, through planned audit, visit, liaison and follow up supplier MAP execution as necessary.

2. 对发生的材料类的符合项、质量事故，配合内部（强生生产车间、实验室等）客户，跟踪、督促供应商展开调查，确保落实切实有效的纠正及必要的改进预防行动。协助海外强生公司处理中国供应商的材料相关的投诉。
In partnering with internal (eg. Production workshops, QA Lab etc.) customers, coordinate, lead, track, review and close of necessary investigation around non-conforming material or associated quality incidences, and ensure effective correction, and corrective / preventive actions as necessary, is implemented at supplier site. Support oversea J&J affiliates to handle material complaint for suppliers located in China.

3. 配合公司的成本改进、可持续业务等项目的要求，提供对供应商质量管理系统及能力的评审、建议。对潜在目标供应商进行能力完善，使达成强生的标准。
Provide preliminary assessment to candidate suppliers about quality system capability, in support to company Cost Improvement Projects, Business Continuity Projects. Develop and execute qualification program to lift potential new / alternative suppliers up to J&J standards.

4. 参与涉及供应商的业务活动（包括新产品、本地化活动等）中的风险识别、评估，确保有效地风险控制手段及其实施，如供应商工艺认证等。
Participate and/or lead risk impact assessment for changes involving suppliers (including New Product Introduction, manufacture relocation, etc.), ensure appropriate risk mitigation plan and approach is identified and executed, including process validation at suppliers, etc.

5. 为其他强生子公司专用的、设址在本地的供应商质量体系的评估提供人员及审计支持。
Leverage personnel and professional resources for on-site quality system audit for China based manufacturing suppliers used exclusively by overseas J&J affiliates.

6. 协调小组成员及时更新、维护与供应商管理有关的数据库和操作流程文件，保证信息的高度准确与完整，包括合格供应商清单及当前审核结论、质量协议、材料投诉清单等关键要求。
Coordinate group member to maintain and update, in timely manners, supplier management related database and SOPs to ensure high level of data accuracy and integrity, including SOPs for supplier qualification and management, key information as approved supplier, corresponding latest audit status, Quality Responsibilities Agreement, Material NC list, etc.

其它 Others:

7. 协助建立、实施并维护适用于对口管辖部门的必要标准作业规范，并为流程的有效性和效率提供持续改进建议。对口管辖部门包括采购部、计划部。
Assist establish and maintain necessary standard operating procedures for partnering functions, and provide recommendation for continued improvement for process effectiveness and efficiency. Partnering functions including Sourcing, Planning.

8. 作为公司内部质量审核成员之一，按审核计划所分配的审核任务活动，包括预备沟通、实施审核、完成报告、复核整改方案及跟踪结案等事宜。
Acting as one internal lead auditor, complete audit program as assigned, including pre communication, audit execution, reporting, corrective action plan review and follow-up for final closure.

人员资质、经历

Personnel Qualification

1. 教育背景 Education Background

ü 化学、制药或相关学科本科或以上学历。

Bachelor degree or above preferred on Chemistry, Pharmacy or other relevant science.

2. 相关经验 Relevant Experience

ü 熟悉了解化妆品、医疗器械及药品相关的国内国际质量体系及法规要求, 以及质量体系的建立及其合规维护。

Good understanding of regulatory and other international requirements on drug, medical device and cosmetics. Previous knowledge and experience in establish and maintenance of quality system and compliance.

ü 熟悉化妆品、医疗器械及药品的制造流程及原辅料的现场使用，了解主要原料的功能特性。

Familiar with manufacturing processes for cosmetic, medical device products and material handling at production shop floors. Understand functionality and/or feature of key materials.

ü 常见质量体系（如ISO9001）的独立审核经历。

Capability to carry out independent quality system audit, e.g. ISO 9001.

ü 至少3年以上相关工作经验。

At least 3 years related working experience.

3. 其他技能 The Other Skills

ü 拥有强有力的领导力，掌握丰富的团队合作及沟通技巧，擅长处理和协调复杂事件或变更，精于数据分析和逻辑思维。

Strong leadership, well communication & team collaboration skills, complexity/change handling, negotiation, good analytical skill/logical thinking

ü 英文流利，说写自如

Fluent English in both writing and speaking.

ü 熟练操作各办公应用软件

Good knowledge of Computerized Software

ü 工作汇报技巧娴熟

Good presentation skills

拥有125年历史的美国强生公司是世界上最具综合性、业务分布范围最广泛的健康护理产品的制造和服务企业，为消费品、制药以及医疗器材和诊断产品市场提供全面的产品和服务。强生公司连续多年名列《财富》“全球最受尊敬的公司”排行榜前列。
 
强生公司一致注重在中国的发展，强生（中国）有限公司1992年在上海市闵行经济技术开发区成立，是强生公司在中国大陆设立的首家独资企业，致力于生产和推广高品质的适合各种年龄段的个人卫生护理用品，推动中国家庭健康护理水平的提高，公司的产品不仅供应国内消费品市场，而且还出口供应国际市场。强生（中国）有限公司的使命是成为中国最受信赖的消费类健康保健公司。公司致力于生产和销售高品质的个人保健产品，以增进中国家庭的健康。
 
With more than 100 years of history, Johnson & Johnson (JNJ) is the world’s most broadly based healthcare company discovering, developing, and manufacturing consumer health, pharmaceuticals, and medical devices and diagnostics products. With over 250 operating companies, Johnson & Johnson has approximately 114,000 employees in 57 countries and markets its products throughout the world. It has been ranked among the top of the global Most Admired Companies by Fortune for years.
Johnson & Johnson has been committed to its development in China. Established in Shanghai Minhang Economic & Technological Development Zone in January 1992, Johnson & Johnson China Ltd. is the first wholly-funded enterprise set up by Johnson & Johnson. It is committed to producing and promoting high quality personal health care products catering for consumers of various ages, and driving the health care of Chinese families. Its products are not only sold in domestic consumer market, but also exported to international markets. The mission of Johnson & Johnson China Ltd. is to become the most reliable consumer health care product provider in China. It is committed to producing and selling high quality health care products to enhance the health of Chinese families.
 
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