Sr Packaging Engineer

Job description

We anticipate the application window for this opening will close on - 8 Sep 2026 Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact. A Day in the Life The Cardiac Surgery Packaging Engineering team supports the development, sustainment, and continuous improvement of sterile packaging systems for medical devices across the product portfolio. The team partners closely with manufacturing sites, quality, regulatory, supply chain, and product development teams to ensure packaging solutions protect product integrity, support patient safety, and meet global regulatory and quality requirements. Responsibilities include sterile barrier design, packaging validation, sustaining engineering activities, compliance initiatives, and manufacturing support. This position is based in Dexter, Michigan. The role follows a flexible work arrangement with an on-site presence expected four days per week and one remote workday per week. The Senior Packaging Engineer supports both sustaining and continuous improvement activities for sterile packaging systems used across the Cardiac Surgery portfolio. This role is responsible for packaging design changes, validation activities, compliance initiatives, manufacturing support, and technical problem solving to ensure packaging systems remain compliant, reliable, and cost effective throughout the product lifecycle. Primary Responsibilities Lead sustaining packaging initiatives, including design changes, supplier changes, corrective and preventive actions (CAPAs), cost reduction projects, and supply continuity activities. Evaluate released product changes for potential impact to packaging configurations and determine appropriate testing, validation, or redesign requirements. Design, develop, and maintain sterile barrier systems, packaging components, assemblies, and specifications in accordance with applicable regulatory and quality standards. Plan and execute packaging verification and validation activities, including protocol development, testing, analysis, reporting, and documentation. Partner with manufacturing sites and distribution centers to troubleshoot packaging issues, support packaging processes, and provide technical guidance for repackaging operations. Support remediation and compliance initiatives, including audits, regulatory submissions, standards assessments, regulation reviews, tender requests, and field complaint investigations. Assess packaging materials, processes, and configuration changes to support quality, manufacturability, cost, and sustainability objectives. Serve as a packaging subject matter expert on cross-functional teams by managing deliverables, identifying risks, and driving continuous process improvements. Required Qualifications Bachelor’s degree and 4+ years of packaging engineering, manufacturing engineering, product development engineering, or related engineering experience; or an advanced degree and 2+ years of relevant engineering experience. ​ Preferred Qualifications Bachelor of Science in Packaging Engineering and 5+ years of packaging engineering experience, or an advanced degree in Packaging Engineering and 3+ years of packaging engineering experience. Experience within the medical device industry or another highly regulated manufacturing environment. Working knowledge of ISO 11607, ISO 13485, Design Control requirements, and medical device quality system processes. Experience with sterilization methods, sterile barrier systems, biomedical materials, and medical packaging design practices. Experience applying root cause analysis, CAPA management, Lean principles, Six Sigma methodologies, project management practices, and supply chain collaboration. Experience supporting packaging design, packaging validation, or sterile barrier systems within a regulated manufacturing environment. Experience developing technical documentation, executing testing activities, and supporting product or process changes through quality management system requirements. Knowledge of packaging materials, packaging processes, and engineering problem-solving methodologies. For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required. Physical Job Requirements The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. U.S. Work Authorization & Sponsorship At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Ro