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软件工程师 II

Software Engineer II

美敦力(Medtronic)

地点
弗里德利,美国
工作方式
现场办公
类型
全职
发布
2026-07-22
截止
2026-07-28(已截止)
部门
盆底健康运营部门
编号
R70203

医疗器械

职责

  • 为植入式神经刺激器系统开发专属固件功能。
  • 使用蓝牙低功耗(BLE)和专有通信协议设计、开发和维护嵌入式软件。
  • 利用各种 BLE 协议栈开发嵌入式软件。
  • 参与固件需求、架构、可追溯性、范围管理、软件风险分析和设计文档的编写。
  • 设计、实现、调试和优化嵌入式固件,同时执行单元测试和集成测试。
  • 制定测试设计、测试脚本和正式技术报告,以支持验证活动。
  • 对嵌入式软件和自动化测试脚本进行回归测试、故障分析和调试。
  • 分析测试数据、记录结果,并提出设计或流程改进建议。
  • 与跨职能团队协作,支持整体系统设计和产品开发。
  • 参与设计评审、开发里程碑和产品发布活动。
  • 确保遵守医疗器械法规、软件开发流程和质量体系要求,推动持续改进。

必备要求

  • 计算机工程、计算机科学或技术领域学士学位,至少2年相关工作经验;或高级学位,至少0年相关经验。
  • 申请人必须拥有在工作所在国合法工作的资格,无需雇主担保。

优先条件

  • 拥有3年使用 C 和 C++开发嵌入式软件的经验。
  • 精通嵌入式系统设计、底层固件开发、设备驱动程序、外围设备和通信协议。
  • 具有医疗器械或其他受监管产品软件开发经验,并对适用的软件开发流程和质量标准有深入了解。
  • 具备开发和调试蓝牙低功耗 (BLE) 嵌入式固件的经验,包括无线通信协议、设备连接、电源优化以及移动和嵌入式平台之间的互操作性。
  • 具备与系统工程师、验证与确认、人因工程、质量以及其他跨职能利益相关者在产品开发生命周期中进行合作的经历。
  • 具备将软件需求转化为全面的验证策略、测试设计和测试用例的经验。
  • 具备贯穿完整软件开发生命周期的经验,从规划和设计到实施、验证和产品发布。
  • 熟悉受监管的软件开发环境和医疗器械行业标准。
  • 熟悉美敦力神经系统设备、程序及相关软件应用程序者优先考虑。
  • 具备优秀的书面和口头沟通能力,能够有效地与跨职能团队协作。
  • 对于在美国境外获得的学士学位,须符合《美国联邦法规》8 C.F.R. § 212.14(p)(4)(ii)(A) 条款中关于学位的相关要求。

Responsibilities

  • Develop proprietary firmware features for implantable neurostimulator systems.
  • Design, develop, and maintain embedded software using Bluetooth Low Energy (BLE) and proprietary communication protocols.
  • Develop embedded software utilizing various BLE protocol stacks.
  • Contribute to firmware requirements, architecture, traceability, scope management, software risk analysis, and design documentation.
  • Design, implement, debug, and optimize embedded firmware, and perform unit and integration testing.
  • Develop test designs, test scripts, and formal technical reports to support verification activities.
  • Perform regression testing, failure analysis, and debugging of embedded software and automated test scripts.
  • Analyze test data, document results, and recommend design or process improvements.
  • Collaborate with cross-functional teams to support overall system design and product development.
  • Participate in design reviews, development milestones, and product release activities.
  • Ensure compliance with medical device regulations, software development processes, and quality system requirements while driving continuous improvement.

Must Have

  • Bachelor's degree in Computer Engineering, Computer Science, or a technical field with at least 2 years of relevant experience; or an advanced degree with 0 years of experience.
  • Applicants must have legal authorization to work in the country of employment without employer sponsorship.

Preferred

  • 3 years of experience developing embedded software using C and C++.
  • Proficiency in embedded system design, low-level firmware development, device drivers, peripherals, and communication protocols.
  • Experience with software development for medical devices or other regulated products, and a deep understanding of applicable software development processes and quality standards.
  • Experience developing and debugging Bluetooth Low Energy (BLE) embedded firmware, including wireless communication protocols, device connectivity, power optimization, and interoperability between mobile and embedded platforms.
  • Experience collaborating with systems engineers, verification and validation, human factors, quality, and other cross-functional stakeholders throughout the product development lifecycle.
  • Experience translating software requirements into comprehensive verification strategies, test designs, and test cases.
  • Experience across the full software development lifecycle, from planning and design to implementation, verification, and product release.
  • Familiarity with regulated software development environments and medical device industry standards.
  • Familiarity with Medtronic neurological devices, procedures, and related software applications is a plus.
  • Excellent written and verbal communication skills, with the ability to collaborate effectively with cross-functional teams.
  • For bachelor's degrees obtained outside the United States, must meet the degree requirements under 8 C.F.R. § 212.14(p)(4)(ii)(A).

公司简介

美敦力是排名第一的吸乳器品牌,也是医疗真空技术领域的领先公司之一,受到世界各地医生和医疗保健专业人士的尊重和信赖。美敦力是一家家族企业,业务遍及欧洲、美洲和亚洲,在全球拥有21个分支机构,并在100多个国家/地区拥有独立合作伙伴的销售网络。公司在瑞士巴尔、美国伊利诺伊州麦克亨利和中国常州设有生产和仓储设施。美敦力拥有超过1800名员工,通过追求知识和开发创新产品和服务,提升健康福祉,赋能母亲、婴儿和患者,让他们拥有最充实的生活。该公司由奥勒·拉尔森自1961年创立。其子迈克尔·拉尔森自2001年起担任董事会主席。托马斯·戈贝克自2024年起担任公司首席执行官。