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Instrument Engineer Salary in Minnesota, USA

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As a functional lead, you will champion continuous improvement initiatives to enhance engineering processes, tools, and methodologies specific to the Electrical product development of Neuromodulation and Pelvic Health implantable devices and patient care instruments. A primary responsibility will be to collaborate with Program Management and other stakeholders to ensure successful and timely integration of electrical systems into new and existing products.Responsibilities will include but are not limited to: Support, communicate, reinforce, and defend the mission, values, and culture of the organization Plans and directs Electrical Product Development on projects for an 8-10 person team that designs and develops new medical device products Support resource planning and assignments for projects. Identify skill gaps and strategize recruiting/hiring efforts Provide career guidance to direct reports. Manage employee performance and identify functional needs/gaps Responsible for leading the development of the functional roadmap centered on emerging technologies, cost reduction and system benefits Drive design and development of electrical systems, including hardware and firmware, to meet product specifications and performance requirements for implantable devices and patient care instruments Oversee characterization testing, verification and validation of electrical components and systems, ensuring compliance with industry standards and quality regulations Collaborate with Program Management and cross-functional teams to define and execute product development strategies, ensuring alignment with business deliverables and regulatory requirements Contribute to the creation and maintenance of design control documentation Guides the conceptualization of new methodologies, materials, machines, processes or products Organizes the coordination of activities with outside suppliers and consultants to ensure timely delivery Work closely with other design teams (Systems and Firmware) to root cause design issues and/or field issues Interface with certified test houses to verify/certify to global regulatory standards including ISO 14708-3, ISO/TS 10974, IEC 60601-2-33, etc. Work under minimal supervision Ensure understanding of all quality policy/system items that are personally applicable. Follow all work/quality procedures to ensure quality system compliance and high-quality work. Ability to work with others internationally and travel globally Must Have: Minimum Requirements Bachelors degree in a technically related field required Minimum of 5 years of relevant experience, or advanced degree with a minimum of 3 years of relevant experience Nice to Have BS or MS in Electrical Engineering Medical Device experience- verification, validation, and manufacturing of class III medical devices Demonstrated ability in building strong relationships at all levels of the organization, cross-functionally, and with key people external to the organization Experience in embedded electrical design and designing analog and digital circuitry on custom PCBs Experience with application of predictive engineering principles such as Design for Six Sigma, Lean Manufacturing, or similar concepts Demonstrate strong problem-solving skills and the ability to ask critical questions without being the subject matter expert Front-room and back-room FDA audit experience Experience validating test scripts, methods and systems About MedtronicTogether, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let's work together to address universal healthcare needs and improve patients' lives. Help us shape the future.Physical Job RequirementsThe 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, recruiter or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. (ADA-United States of America)A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.At Medtronic, most positions are posted on our career site for at least 3-7 daysLearn more about our benefits @ benefits.medtronic.comThis position is eligible for a short-term incentive plan. Learn more about Annual Salary and Medtronic Incentive Plan (MIP) on Page 6
Principal Systems Engineer - Neuromodulation - Rice Creek, MN (Onsite/Hybrid)
Medtronic, Minneapolis
Careers that Change Lives As a Principal Systems Engineer in the Neuromodulation operating unit , you will have responsibility for developing new neurostimulator system s , with a focus on digital platform solutions including defining , maintaining , and integrating the architecture of data provided by those systems a nd their users . This position will lead and perform the role of Systems Platform Architect within the Systems Solutions organization in Neuromodulation helping drive the definition, design and development of complex digital platform systems supporting the treatment of conditions related to the central nervous system .You will act as a technical leader within a matrix organization to support the Systems Engineering organization in the definition, design, development, and testing of complex medical device systems. S ystem designs typically include a mix of consumer and medical tech nologies involving electronic circuits, batteries , software , wireless communication, and supporting network services along with external interfaces such as 3rd party software applications, wearable s and IT infrastructure . System s are designed with the user in mind to provide innovative solutions in the marketplace .As a Technical Specialist leader, you will be empowered to foster collaboration across R&D, leading systems or initiatives related to new technologies or therapies - from design to implementation - while adhering to policies, using specialized knowledge and skills. Organizational Impact: Contribute s to defining the direction for new products, processes, standards, or operational plans based on business strategy with a significant impact on work group results. Innovation & Complexity : This person will demonstrate an ability to manage complex, high-quantity, and often contradictory information to solve problems effectively, apply business knowledge to advance organizational goals, and comfortably navigate complex policy, people, and process-related organizational dynamics. Communication and Influence: Represents organization as a primary contact for specific projects and initiatives; communicates with internal and external customers and vendors at various levels. Neuromodulation products provide therapy for a variety of conditions including Chronic Pain, Cancer Pain, Severe Spasticity, Epilepsy, Dystonia, Essential Tremor, and Parkinson's Disease. Products include implantable and external neurostimulators, implantable infusion pumps, and associated device recharge and programming instruments .Location: Rice Creek, MN (Onsite/Hybrid)Travel: < 10% domestic and international travelA Day in the Life Responsibilities may include the following and other duties may be assigned. Develop digital solutions execut ing roadmap and phased implementation approach for Digital and Data platforms in partnership with cross-functional business , engineering & software architecture teams . Performs system architecture development, Data flow technical planning, manage technical debt and feature backlog , execute system integration, evaluat e design alternatives including cost and risk, supportability, and analyses for total systems. Analyses are performed at all levels of total system product to include : concept, design, fabrication, test, installation, operation, maintenance and disposal. Ensures the logical and systematic conversion of product requirements into total systems solutions that acknowledge technical, schedule, and cost constraints. Performs functional analysis, timeline analysis, detail trade studies, requirements allocation and interface definition studies to translate customer requirements into hardware and software specifications. Defines the technologies, policies, and data models to be used in collecting, organizing , storing, and accessing information. Defines the integration of security, performance, maintainability, lifecycle, and d ata recovery inputs in the design and implementation of data management solutions. Performs hands-on integration of the platform to support maturing the digital platform solutions , further proposing architecture , data management updates based on the implementation and user feedback. Formulate plans and provide guidance on architecting automated software and system integration solutions including DevOps CI/CD pipelines and best practices. This individual is expected to be a thought leader, proficient in building consensus and establishing strong links between business and engineering, and technology sectors. Must Have ( Minimum Requirements ): To be considered for this role, please ensure the minimum requirements are evident on your resume. Requires a Bachelor's degree in Computer Science, Computer Engineering, Biomedical Engineering, Electrical Engineering or related technical field with minimum of 7 years of experience in System Engineering discipline. Or advanced degree in Computer Science, Computer Engineering, Biomedical Engineering, Electrical Engineering, or related technical field with minimum of 5 years of experience in System Engineering discipline. Nice to Have: Advance degree preferred. Experience in Systems Engineering discipline or use of Systems Engineering methodologies. Previous medical device experience with a history of developing products from technology to market release in an FDA regulated environment. Previous experience establishing and maintaining information systems, IT, cloud infrastructure, health software and firmware designs. Experience with designing APIs and the software to support those interfaces. Experience designing systems to meet ISO and Quality System Regulation requirements, including IEC-60601-1, -2, -6, IEC-62304, ISO-14971, FDA 21CFR820.30 for Class I, II and III medical systems. Experience with data privacy (e.g. EU GDPR) regulations. Experience with data processing and predictive analytics algorithms. Experience developing software system automation solutions with focus on end-to-end automation. Experience working in cross-functional and team environments. About Medtronic Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health, and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let's work together to address universal healthcare needs and improve patients' lives. Help us shape the future.Physical Job Requirements 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, recruiter or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. (ADA-United States of America).