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此界面为简体中文。雇主发布的职位名称和描述保留原文,可能为英文。

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Quality Systems Manager

Nextern

地点
Maple Grove, Minnesota, United States
发布日期
2026年10月19日

申请前,请在雇主网站确认职位仍在招聘,并检查完整要求和条件。

职位描述

此界面为简体中文。雇主发布的职位名称和描述保留原文,可能为英文。

NPX Medical is a division of Nextern — a global, vertically integrated medical device development and manufacturing platform. We specialize in precision metal components and assemblies, with deep expertise in nitinol engineered components, precision laser cutting and processing, and advanced catheter technologies. Our engineers bring decades of combined experience — from R&D and rapid prototyping through full commercial production. At Nextern, we inspire with passion, impact with significance, and act with integrity. Nextern partners with OEMs, clinicians, and innovators to design, develop, and manufacture world-class medical devices across the full product lifecycle. From single-use disposables to fully integrated systems to precision components, our teams work as an extension of yours to solve patient needs and improve lives worldwide. The Quality Systems Manager will be responsible for strategy deployment, alignment, and standardization of the Quality Management System and Quality Systems Team (engineers, technicians, and inspectors). You will own the audit, certification, and relationship maintenance of the company’s notified body and regulatory agency registration processes and coordinate global leadership teams to properly resource and prioritize initiatives relating to facility certification business strategies. You will oversee the programs, policies, processes, procedures, and controls ensuring that performance and quality of products conform to established standards and agency regulations. RESPONSIBILITIES: Directly manage the relationships between NPX Medical and their ISO notified body. Directly manage the Quality Systems Team in effectively establishing scalable and compliant systems and processes (i.e. CAPA, Change Control, Document Control, Customer Feedback, Training, etc) and supporting Customer, Internal & Regulatory Audits. Lead compliance initiatives for core QMS processes and standardization of quality metrics. Define and communicate overall vision and cascade objectives for the department. Develop, train, implement and continuously approve upon company and business unit policies and procedures. Provide timely performance & developmental evaluations of departmental staff. Ability to work effectively within a team in a fast-paced changing environment. Strong organizational, planning, and follow-up skills and ability to hold others accountable. Directly supervises employees within the Quality Systems Team. Responsibilities include interviewing, hiring, and training employees; planning, assigning, and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems. Required: Bachelor’s degree in a STEM related field 7+ years of relevant experience in ISO 13485 and FDA GMP. 2+ years of Quality management experience Excellent Written & Oral Communication Skills. Experience with configuration of reports, security/access, data structuring, meta-data fields, and workflows. Medical device experience Preferred: Experience in implementing foundational and expandable quality system strategies in a small-mid size company. Project management experience in transitioning to the ISO 13485:2016 standard. Project management experience in implementing an eQMS systems. Training/certification in Lean and Six Sigma Training/certification in lead auditing ISO 13485 and FDA GMP systems Previous CDMO experience Salary range: $120,000 to 160,000 depending on skills and experience Health Care Plan (Medical, Dental & Vision) Retirement Plan with Company Match Paid Time Off, Personal Days, AND Birthday Holiday! Lifetime Membership Subsidy and Wellness Resources Life Insurance (Basic, Voluntary & AD&D) Family Leave (Maternity, Paternity) Short-Term & Long-Term Disability Taco Thursdays!!! Nextern is an equal opportunity employer. We encourage applications from candidates of all backgrounds and experiences, and we are committed to fostering an inclusive and diverse workplace. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

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选择能够回应职位要求的真实经历,说明你的贡献,只使用能够证实的数字。遵循雇主的申请说明,并在提交前检查联系方式、文档内容和 PDF。

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求职常见问题

为什么有些职位使用英文?

职位名称和描述由招聘企业撰写。为避免改变招聘要求或工作条件,我们保留原文。操作界面和本指南使用简体中文。如果中文搜索没有结果,可以尝试使用职位发布语言中的名称或技能,例如“software engineer”。搜索词不会自动翻译,界面语言也不代表企业要求的申请语言。

远程职位是否允许从任何国家工作?

不一定。企业可能对居住国家、工作许可或工作时段有要求。请查看原始招聘页面中的具体条件。如果未说明,应先向企业确认,再判断能否从你所在的地区工作。“远程”标签本身并不代表没有地点限制。

搜索没有结果时应该怎么办?

尝试更通用的职位名称或单个技能,并逐一移除筛选条件。不同企业可能用不同名称描述相似工作。如果某个职位已经消失,请在企业招聘页面搜索其职位编号。扩大搜索范围不会让已经关闭的职位重新开放。

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申请按钮会打开外部网站。请按照企业或招聘服务的说明,在该网站完成并确认提交。在 ResumizeAI 中准备简历并不等于已经申请职位。如果链接只打开企业网站,请先找到对应职位,再继续申请流程。

如何针对职位调整简历和求职信?

将招聘要求与能够解释清楚的项目、任务和成果联系起来。突出相关经历,不要添加未经实际掌握的技能或虚构成绩。在求职信中用具体例子说明申请动机,并遵守企业要求的语言和文件格式。提交前检查两份文件,确保内容准确、联系方式正确、链接可用。