资深机械工程师 – 机器人主机设备（医疗器械）

该职位来源于猎聘 Summary The Staff Mechanical Engineer is a senior individual contributor responsible for leading the design, development, and integration of mechanical subsystems for complex medical robotic capital equipment. This role requires deep mechanical expertise, strong ownership from concept through commercial launch, and the ability to work effectively within regulated environments. The ideal candidate is a proactive “go‑getter” who partners closely with electrical, software, and systems teams, contributes to system‑level decisions, and communicates fluently across global organizations. Professional proficiency in spoken and written English and Mandarin is required to support international collaboration with suppliers and manufacturing partners.

Key Responsibilities Mechanical Design & Development Lead the mechanical design, development, and integration of complex electromechanical subsystems for robotic capital equipment, including structures, mechanisms, actuation systems, and thermal solutions. Own the mechanical design lifecycle from concept through production, including prototyping, verification, validation, and manufacturing support. Perform detailed mechanical analysis using advanced CAD and analysis tools (e.g., SolidWorks, FEA, tolerance stack‑ups, GD&T) to ensure performance, reliability, and robustness. Manufacturing & Cost Leadership Drive DFM/DFA activities with cross‑functional teams and suppliers to enable scalable, repeatable production. Lead cost optimization initiatives, including material selection, process trade‑offs (machining, injection molding, casting, sheet metal), and supplier strategy. Support supplier development, tooling reviews, and manufacturing readiness efforts. System Integration & Cross‑Functional Collaboration Collaborate with Systems, Electrical, Software, Quality, and Manufacturing Engineering teams to ensure seamless electromechanical integration. Actively participate in system‑level architecture discussions as the mechanical domain expert, ensuring mechanical designs align with overall product requirements. Support root‑cause investigations, failure analysis, and corrective actions for mechanical issues. Regulatory & Quality (Medical Device) Create and maintain comprehensive mechanical design documentation, including models, drawings, specifications, and DHF deliverables. Participate in DFMEAs, verification and validation activities, and design reviews within an ISO 13485 / FDA design controls framework. Support regulatory submissions and external audits as the mechanical subsystem subject‑matter expert. Communication & Global Collaboration Serve as a key technical interface with international manufacturing partners and suppliers. Communicate technical content clearly in English and Mandarin, including drawings, specifications, and design reviews.

Required Qualifications B.S. or M.S. in Mechanical Engineering or a related field. 8+ years of experience in product design and development, including work on medical devices, robotics, or other highly regulated, high‑reliability systems. Minimum 3 years of this must be medical. Proven experience designing and launching complex electromechanical or robotic capital equipment. Expert knowledge of DFM/DFA and demonstrated success driving cost‑effective, manufacturable designs. Proficiency with 3D CAD and mechanical analysis tools. Professional proficiency in spoken and written English and Mandarin Chinese. Demonstrated “go‑getter” attitude with strong ownership and execution skills.

Preferred Qualifications Experience with surgical robotics, minimally invasive systems, or precision automation. Deep knowledge of injection molding, tooling, and sheet‑metal fabrication. Experience with CAPA, failure investigations, and root‑cause analysis. Working knowledge of electronics packaging and thermal management.

公司简介 天津普利方舟医疗科技有限公司（以下简称“普利方舟医疗”）是美国 Noah Medical 在中国的全资子公司。普利方舟的百川系统为Noah Medical的Galaxy系统在中国国产化替代产品。

产品基于我们全新一代的医疗机器人平台开发，致力于为肺部疾病患者提供全新的早期诊断和治疗方案。

全球现已拥有超400人的精锐团队，我们不仅拥有行业先进的技术，更有来自世界众多知名医疗公司的管理层人员，具备敏锐的洞察力以及丰富的创造力。

期望在我们的努力下，打造出革命性的新一代手术机器人产品，造福于人类。

概述 资深机械工程师是高级个人贡献者岗位，负责领导复杂医疗机器人资本设备机械子系统的设计、开发与集成。 该岗位要求具备深厚的机械专业能力、从概念到商业化上市全过程的强烈责任感，以及在受监管环境中高效工作的能力。 理想候选人应积极主动、执行力强，能够与电子、软件和系统团队紧密合作，参与系统级决策，并能在全球组织中流畅沟通。 为支持与供应商及制造合作伙伴的国际协作，候选人必须具备良好的中英文口头和书面沟通能力。

关键职责 机械设计与开发

• 负责机器人资本设备复杂机电子系统的机械设计、开发与集成，包括结构、机构、驱动系统和热管理解决方案。
• 负责机械设计全生命周期，从概念设计到量产，包括原型开发、验证、确认以及制造支持。
• 使用先进的 CAD 和分析工具（如 SolidWorks、有限元分析 FEA、公差叠加分析、GD&T）进行详细机械分析，以确保性能、可靠性和稳健性。

制造与成本领导力

• 与跨职能团队和供应商推动 DFM/DFA 活动，以实现可扩展、可重复的生产。
• 主导成本优化工作，包括材料选择、工艺权衡（机加工、注塑、铸造、钣金）以及供应商策略。
• 支持供应商开发、工装评审和制造就绪性相关工作。

系统集成与跨职能协作

• 与系统、电气、软件、质量和制造工程团队协作，确保机电集成无缝衔接。
• 作为机械领域专家，积极参与系统级架构讨论，确保机械设计符合整体产品需求。
• 支持机械问题的根因调查、失效分析和纠正措施制定。

法规与质量（医疗器械）

• 创建并维护完整的机械设计文档，包括模型、图纸、规范以及 DHF 交付物。
• 在 ISO 13485 / FDA 设计控制框架下，参与 DFMEA、验证与确认活动以及设计评审。
• 作为机械子系统主题专家，支持法规申报和外部审核。

沟通与全球协作

• 作为与国际制造合作伙伴和供应商对接的关键技术接口。
• 能够使用中英文清晰传达技术内容，包括图纸、规范和设计评审。

任职要求

• 机械工程或相关专业学士或硕士学位。
• 8 年以上产品设计与开发经验，包括医疗器械、机器人或其他高监管、高可靠性系统相关工作经验，其中至少 3 年必须为医疗器械领域经验。
• 具备复杂机电设备或机器人资本设备设计及导入上市的成功经验。
• 精通 DFM/DFA，并在推动高性价比、可制造设计方面有明确成功记录。
• 熟练使用 3D CAD 和机械分析工具。
• 具备专业水平的中英文口头和书面表达能力。
• 具备积极主动、结果导向的工作态度，以及强烈的责任心和执行能力。

优先条件 有手术机器人、微创系统或精密自动化相关经验者优先。 深入了解注塑、工装和钣金制造。 具备 CAPA、失效调查和根因分析经验。 具备电子封装和热管理的工作知识。