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浏览职位招聘观察购买与订阅
DSM-Firmenich logo
帝斯曼芬美意
Single Position
立即应聘

Single Position

发布于 5 个月前

普通员工/个人贡献者

Exton (PA), United States
中级经验
全职员工
仅现场办公
高中/中专
生产制造
化学合成
叉车驾驶
设备维护
GMP
ISO 13485
MS Office
SAP
危险废物处理
反应器操作

AI 估算 · 35k–42k

该岗位要求3年以上化工制造经验,需掌握GMP、设备操作等专业技能,属于技术实操岗。跨国企业平台提供稳定薪酬和福利,薪资在同类技术岗位中具备竞争力。

职位详情

关于这个职位

这是一个生物医学制造领域的生产技师岗位,主要负责在GMP(良好生产规范)环境下,动手合成帝斯曼芬美意的生物医学产品

你需要操作反应器、挤出设备等,并负责物料的称量、设备清洁维护、危险废物处理以及准确的生产记录
这是一个需要严格遵守安全与质量规程的实操性技术岗位

最低要求

高中毕业

在化工或工业制造工厂/车间拥有超过3年的相关经验
必须具备对所学常规、程序、实践和更复杂技能的知识
需要接受特定程序或设备的培训
必须具备良好的化学品安全和卫生知识
需要良好的文件记录和沟通技巧
具备遵循口头和书面技术指导的资质和能力
守时、积极主动、可靠且注重细节
熟练使用 MS Word、Excel 和 Outlook

工作职责

根据帝斯曼芬美意质量体系和既定操作规程,亲手合成生物医学产品

完成生产和工程批次合成所需原材料的称量和分配
确保反应器及辅助设备清洁并准备就绪
负责操作、拆卸、重新组装和清洁所有用于合成生物医学产品的反应器、挤出设备、压力罐及其他辅助设备
根据需要提供筛分、包装、GMP标签程序和挤出支持
可能需要支持培训其他团队成员
演示流程步骤以进行在职培训
负责记录和维护加工化学品、仓库清洁溶剂的运行库存,并根据GMP日志和SAP正确记录这些材料的消耗
处理日常产生的危险废物,并根据需要为此流程向其他团队成员提供培训
负责制造设备的简单维修和预防性维护
维护反应器、压力容器、泵、阀门设备
能够在Blue Mountain中根据需要为设备维修创建工作订单
遵循帝斯曼芬美意/GMP指南,保持所有生产活动的详细准确记录
在制造区域和设备上保持良好的清洁规范
每天在指定系统中准确记录工时和考勤要求
立即向主管、管理层或安全委员会成员报告任何观察到的设备不安全状况或操作
遵守帝斯曼芬美意质量体系程序以及ISO 9001和ISO 13485标准
准确记录制造操作,遵循帝斯曼芬美意质量体系程序
在分配并经过适当培训后,执行必要的任务组合,以确保危险材料得到正确处理、分类和存储
执行必要的工作,以根据所有适用的地方、州和联邦法规对废物进行表征和描述
这包括:
表征废物并应用正确的废物代码和标签
审查任何异地运输的清单
在废物运输期间协助运输商
保持危险材料存储区域的良好清洁,并每周检查这些区域
根据指示应对危险材料泄漏

优先资格

具有化工制造工艺和反应器操作经验,并表现出学习和安全工作的能力者优先

有叉车驾驶经验者优先

AI 洞察

优缺点分析

优点

  • Gain hands-on experience in the high-demand and regulated field of biomedical manufacturing within a large, established multinational company.
  • Develop highly transferable skills in GMP compliance, chemical process operations, and hazardous material management, valued across pharmaceuticals and chemicals.
  • Work in a purpose-driven company focused on health and nutrition, contributing to products that impact millions, with opportunities for internal growth and development.
  • Receive a competitive compensation package with comprehensive benefits, typical of a stable, publicly-traded corporation.
  • The role involves hands-on, physical work in a manufacturing environment, which may include shift work, exposure to chemicals, and adherence to strict safety protocols.
  • High attention to detail and rigorous documentation are required to meet GMP and regulatory standards, which can be demanding and leave little room for error.
  • Career progression beyond senior technician or team lead may require additional education or specialization to move into engineering or management roles.
  • This position is ideal for individuals with a hands-on, practical mindset, strong attention to detail, and several years of experience in industrial or chemical manufacturing who seek a stable technical role in a global life sciences company.

缺点 / 挑战

暂无明显挑战项

角色解读

  • Within the manufacturing track, you can advance to senior technician roles, specializing in complex processes or equipment, or move into a team leader position overseeing a production line.
  • With experience in GMP and quality systems, you could transition into roles in Quality Assurance (QA), Quality Control (QC), or Manufacturing Support within the biomedical or pharmaceutical industry.
  • The skills in equipment maintenance and SAP systems could also open doors to roles in facilities management, technical support, or supply chain within large multinational corporations.
  • You will perform hands-on synthesis of biomedical products using reactors and extrusion equipment, following strict GMP and quality procedures.
  • Your daily tasks include weighing raw materials, operating and cleaning manufacturing equipment, and ensuring all processes are documented accurately in systems like SAP.
  • You are responsible for handling hazardous waste generated during production, including its proper classification, labeling, and disposal in compliance with regulations.
  • You will also assist in training team members on processes and safety protocols, and perform minor equipment repairs and preventive maintenance.
  • Practical experience in chemical or industrial manufacturing, specifically with reactor operation and process equipment.
  • Strong understanding and adherence to GMP guidelines, chemical safety, hygiene, and quality standards like ISO 13485.
  • Proficiency in documentation, communication, and following detailed technical instructions, along with basic computer skills in MS Office.
  • Ability to perform tasks safely, handle hazardous materials, and maintain accurate records of all production activities.

申请策略

  • Research dsm-firmenich's business areas, particularly their biomedical and nutrition segments, to understand the context of your work and align your application with their purpose.
  • Emphasize your reliability, punctuality, and ability to work as part of a team in a regulated environment, as these soft skills are explicitly valued for this role.
  • Quantify your experience: Clearly state the number of years (e.g., "4+ years") in a chemical/industrial manufacturing facility and specify the types of equipment you've operated (reactors, extruders).
  • Highlight specific skills: Use keywords like "GMP compliance," "hazardous waste handling," "equipment maintenance," "SAP," and "ISO standards" directly from the job description.
  • Showcase safety and quality focus: Describe instances where you followed strict procedures, maintained accurate records, or contributed to a safe work environment.
  • Mention any relevant certifications or training, such as forklift operation, chemical safety, or specific equipment training.
  • If lacking, consider obtaining a basic certification in forklift operation or a short course on GMP fundamentals for manufacturing to strengthen your application.
  • Brush up on your knowledge of key quality standards mentioned, such as ISO 13485, and be prepared to discuss how you've applied similar principles in past roles.

面试指南

  • Use the STAR method (Situation, Task, Action, Result) to structure your answers, especially for behavioral questions about past experiences.
  • Always connect your skills and experiences back to the key requirements of the role: safety, GMP compliance, hands-on operation, and accurate documentation.
  • Demonstrate a proactive and responsible attitude by highlighting instances where you identified a potential issue, followed protocols, and ensured a safe, quality outcome.
  • Walk me through your experience operating reactors or similar chemical processing equipment. Describe a specific batch process you were responsible for.
  • Tell me about a time you had to follow a strict GMP or safety procedure. What was the situation, and what was the outcome?
  • How do you ensure accuracy and attention to detail when documenting production activities or handling raw materials?
  • Describe your experience with handling hazardous materials or waste. What steps do you take to ensure safety and compliance?
  • Have you ever trained a colleague on a process or piece of equipment? How did you approach it?

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