在罗氏，我们鼓励每位同事展现真实的自己；我们欣赏独特且出众的品质。罗氏的文化鼓励积极的表达、开放的对话和真诚的连结，在这里，你将因为做自己而被重视、接纳和尊重，并得到个人的提升和职业的发展。所有的这一切，都是为了更好地预防、阻止和治愈疾病，并确保医疗资源的可及性和可持续性。欢迎加入罗氏，一个重视每种声音的地方。
职位
Primary Purpose of Job (Job Summary)
Responsible for producing innovative oral-solid medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment, and maintain areas in high state of inspection preparedness. Managing operates production equipment for Xeloda/Cellcept that may include process monitoring, sampling, environment monitoring and semi-manufactures transfer operations. Maintains records and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP), Roche PQS, Standard Operating Procedures (SOP). Responsible for being proficient in functional areas and applies expert knowledge of mechanical, scientific principles, processes and pharmaceutical processing equipment.

Principle Roles & Responsibilities / Accountabilities

● Lead manufacturing to implement cGMP in order to guarantee the quality of products and performance according to Roche standards. By reinforcing and monitoring obedience to national and company’s regulation or policy.
● Working with MSAT closely to prepare solutions for the production process, and continues operational improvement.
● Work with coworkers and supervisor to effectively troubleshoot equipment and process issues.
● Understand the theory, concepts, and regulations behind pharm technology and processes. And Provide strong knowledge of manufacturing department with an understanding of E2E process impact.
● Anticipates potential problems and takes preventative action. Requires judgment to know when it is necessary to consult with support groups.
● Trouble shooting for process problems. Understands how own actions impact others and uses this information in decision-making.
● Review documentation and check all calculations.
● Comply with safety requirements, cGMP, SOP and manufacturing documentation. Exhibit detail oriented documentation skills.
● Cooperate with Technical support team Operate automated systems for equipment operation. Assemble and prepare equipment for production.
● Set up professional interpersonal team. Communicate effectively and ability to work in a team environment.
● Follows established safety and environmental guidelines and procedures for all work performed. Immediately reports safety and environmental incidents including injuries, illnesses, near misses, and safety suggestions.
● Provide coaching and training on best practices and compliance to SOPs.
● Participate in the respective projects.
● Participate in and support the projects including but not limited to IQ, OQ, PQ, etc. with high independency and competence.
● Execute the projects and implement the projects.
● Related SAP, MES and CHRIS system operation.

Education/Qualifications

● Bachelor or above
● Pharmaceutical technology or relevant fields

Leadership Competencies

● Models Integrity
● Focus on value and customer
● Align for success
● Deliver results
● Learn for the future

Job Required Competencies

● 5 years’ experience in Pharmaceutical industry
● 3 years’ experience in pharmaceutical manufacturing.
● Excellent oral and written communication skills.
● Capable of writing detailed reports and summaries.
● Must possess high level of automation and technical process knowledge as related to prep and process within area of responsibility.
● Familiarity of computer-based systems.
● Strong ability in organization and coordination
● Strong sense of GMP
● Good team management skill
● Language skills – English & Chinese

我们是谁
打造更健康的未来是促使我们创新的动力。全球超过100,000名员工共同致力于推进科学，确保今天和明天的人们，都能获得高质量的医疗资源。我们的努力帮助了2600多万人使用我们的药物进行治疗，我们的诊断产品运行超过300亿次检测。罗氏通过赋能探索新的可能、激发创造力并保持高标准以提供突破传统的医疗解决方案，对全球的医疗环境带去推动和影响。

让我们一起，构建更健康的未来。

罗氏中国由制药和诊断两大业务领域组成，员工总数超过7000人。作为全球个体化医疗的领导者，罗氏制药和罗氏诊断均在中国建成了完整的价值产业链，包括研究、开发、生产、营销等环节。未来，上海将成为罗氏继巴塞尔和旧金山之后的第三大全球战略中心，而罗氏也将继续践行对中国的长期承诺，满足中国患者的未尽之需。

罗氏提供平等的职业发展机会。