为什么病人需要你

如果没有我们的制药团队，我们的突破将无法到达患者手中。我们依赖于一个由敬业、机智的成员组成的团队，他们了解他们在辉瑞使命中的重要性和影响。患者需要像你这样的同事，他们为自己的工作感到自豪，并总是寻求改善结果。您将帮助确保患者和医生在需要时获得他们所需的药物。

你将取得什么成就

作为技术操作的一部分，你将成为团队成员，对程序、技术、工具、材料和设备有良好的理解。您的决策将帮助您根据可用资源确定工作流的优先级。你将按照标准程序完成任务，其中一些任务可能在范围、顺序、复杂性和时间上有所不同。通过分享您之前获得的知识，您将为团队的成功做出贡献。

正是你们的辛勤工作和专注，将有助于辉瑞为实现新的里程碑做好准备，并帮助全球的患者。

你将如何实现它

• 管理自己的时间和职业发展，对自己的结果负责，并开始优先考虑自己的工作流程。
• 负责各种部件、材料、设备、机器的准备和/或操作，包括但不限于指定区域内的任何和/或所有适用部件、材料、设备、机器。
• 严格遵守所有工厂安全和（当前）良好生产规范{以及cGMP}法规。
• 协助诊断和故障排除活动，并执行过程中质量检查。
• 在开始生产前，确保零件和材料有足够的库存。
• 确定并寻求实施流程和安全改进，以安全的方式执行所有任务。
• 参加值班会议，提供交接信息，并与其他单位和班次沟通。

资格

必须有

高中文凭或GED

2年以上工作经验

能够正确解决工作相关问题，进行良好的判断/决策，并与团队成员有效合作

最好具备

学士学位

有cGMPs工作环境的经验

Why Patients Need You

Our breakthroughs would not make it to the hands of patients without our pharmaceutical manufacturing team. We rely on a team of dedicated and agile members, who understand the importance and impact of their role in Pfizer’s mission. Patients need colleagues like you who take pride in their work and always look to improve outcomes. You will help to ensure that patients and physicians have the medicines they need, when they need them.

What You Will Achieve

As part of technical operations, you will be a team member who is relied to have a good understanding of procedures, techniques, tools, materials and equipment. Your decision making will help you prioritize workflows based on the available resources. You will follow standard procedures to complete tasks, some of which may vary in scope, sequence, complexity and timing. You will contribute to the team’s success by sharing your previously acquired knowledge.

It is your hard work and focus that will help in making Pfizer ready to achieve new milestones and help patients across the globe.

How You Will Achieve It

• Manage own time and professional development, be accountable for own results and begin to prioritize own workflow.
• Responsible for the preparation and/or operation of various components, materials, equipment, machines including, but not limited to any and/or all applicable components, materials, equipment, machines in the assigned area(s).
• Complete adherence to all plant safety and (current) Good Manufacturing Practices {also cGMP} regulations to the highest.
• Assist with diagnosis and troubleshooting activities and execute in-process quality inspections.
• Ensure adequate inventory of parts and materials prior to initiating a production run.
• Identify and seek to implement process and safety improvement and perform all tasks in a safe manner.
• Participate in shift meetings, provide hand off information and communicate with other units and shifts.

Qualifications

Must-Have

• High School Diploma or GED
• 2+ years of experience
• Demonstrates ability to properly problem solve work-related issues, exercise good judgment/decision making, and effectively work with team members

Nice-to-Have

• Bachelor's Degree
• Previous experience in cGMPs (current Good Manufacturing Practices) environment

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Manufacturing#LI-PFE