Careers That Change LivesMedtronic leads the health care industry to provide solutions that benefit the daily lives of people across the globe. Our organization contributes directly to this mission through our rich software system, which include Embedded products, Mobile and Cloud based applications combined with scaled infrastructure and advanced analytics. Become part of our team and you will be challenged to build these amazing software products, and in the process, make a real difference.#MDTDiabetesReferralCampaignAs a Software Design Quality Manager, you will lead the Software Design Quality team focused on Medtronics Embedded device portfolio, you will be asked to manage and guide the design quality engineers in the pre-market design and sustaining space. You will be responsible to drive development of safe, reliable, and compliant products/systems while working very closely with the cross functional teams and building a highly technical and competitive design quality engineers.The best candidates will be critical thinkers, problem solvers, strong executers, self-driven with strong leadership skills & hands-on management approach. Strong relationship skills are a must, as is excellent verbal and written communication.A Day in the LifeResponsibilities may include the following and other duties may be assigned.Plans, directs, and implements all quality aspects of the company's design and development of new and sustaining medical device products or software systems, with detailed focus on software reliability, risk management and patient safety.Provide oversight and training in the application of work processes to ensure successful adoption by development teams and positive, measurable results obtained from development programs.Work closely with cross functional teams and quality peers to ensure project planning is complete end-to-end, for both pre-market and post-market activities.Manages activities to assure programs are appropriately resourced and ensure continuous improvement in technical capability, process, and compliance.Provides oversight for the development and maintenance of quality programs, systems, processes, and procedures that ensure compliance with policies and that the performance and quality of services conform to established internal and external standards and guidelines.Provides expertise and guidance in interpreting policies, regulatory and/or governmental regulations, and internal regulations to assure compliance.Works directly with operating entities to provide process analyses oversight on a continuing basis to enforce requirements and meet regulations.Ensures the quality assurance programs and policies are maintained and modified regularly.Communicate program status using clear metrics and specific actions plans, applying organizational acumen appropriate for a senior level audience.Facilitates uniform standards worldwide and enables best practice sharing, thereby fostering the achievement of company's mission globally.Working knowledge of IEC 62304, 21 CFR 820.30 and ISO 14971Manages feasibility studies of the design to determine if capable of functioning as intended.Selects, develops and evaluates personnel to ensure the efficient operation of the function.Must Have: Minimum RequirementsTo be considered for this role, please ensure the minimum requirements are evident in your applicant profile.Bachelors degree required in Engineering, Science or technical field with 5+ years of experience in the embedded software medical device space and 5 years of technical leadership or managerial experience.ORAdvanced Degree in Engineering, Science or technical field with 3+ years of experience in the embedded software medical device space and 5 years of technical leadership or managerial experience.Nice to HaveDirect experience in software, or systems engineering in a design engineering role.Extensive experience in complex product development projects with strong knowledge of product development in regulated industries (such as medical device, healthcare, aerospace, or transportation industries)Working knowledge of ISO 13485, ISO 14971, 21 CFR 820, IEC 62304, IEC 60601-1 and MDD/EU MDR.Ability to author technical reports, business correspondence and standard operating procedures.Experience in applying metrics to measure and improve processes and product quality during product development.Proven track record of success in leading cross functional efforts in work process improvement.Experience in influencing, educating, and fostering others in adopting work practices.Strong employment history of assuming successive organizational roles with increasing responsibility.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. Lets 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 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. Learn more about our benefitshere (https://www3.benefitsolver.com/benefits/BenefitSolverView?page_name=signon&co_num=30601&co_affid=medtronic).This position is eligible for a short-term incentive plan.Learn more about Medtronic Incentive Plan (MIP) on page 6here.The provided base salary range is used nationally (except in certain CA locations).The rate offered is compliant with federal/local regulations and may vary by experience,certification/education, market conditions, location, etc.Min Salary128400Max Salary192600It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.#J-18808-Ljbffrby Jobble

Senior Supplier Engineering Manager (New Product Development)Careers that Change LivesAt Medtronic, we push the limits of what technology can do to make tomorrow better than yesterday and that makes it an exciting and rewarding place to work. We value what makes you unique. Be a part of a company that thinks differently to solve problems, make progress, and deliver meaningful innovations.The Senior Supplier Quality Engineering Manager is a leadership position responsible for driving world-class supplier quality and reliability for new product introductions.The primary focus of this position is on the Pre-Market Product Development side of the business with a strong emphasis on supplier quality for the design and development. The role involves leading a team of supplier quality engineers across multiple geographic locations ensuring engineering rigor and quality system requirements are applied to suppliers and their processes. This position will establish overall supplier quality engineering strategy and objectives for the new product development projects as well as process improvements to the quality management systems. This position will involve staffing, coaching, and allocating Supplier Quality Engineers.Together with Development team, create/manage a technically rigorous supplier qualification process and efficient pre-market quality system that consistently enables product performance risks to be identified, characterized, and mitigated to meet or exceed stakeholder and project requirements.Peripheral Vascular Health therapies treat patients with Peripheral and Carotid Artery Disease, End-Stage Renal Disease, Superficial and Deep Venous Diseases, and a variety of conditions treated with Peripheral Embolization. The operating unit leads the way in the Superficial Venous, Deep Venous Stenting, AV Access, and Drug-Coated Balloon markets, caring for over 1 million patients globally with lifesaving and life-enhancing therapies.The PVH operating unit offers a diverse portfolio of devices and therapies to treat restore the right blood flow to the right patient.This position is in Plymouth, MN. within the Peripheral Vascular Health (PVH) operating unit and requires on-site presence three days a week.We believe that when people from different cultures, genders, and points of view come together, innovation is the result and everyone wins. Medtronic walks the walk, creating an inclusive culture where you can thrive.A Day in the LifeIn general, the following responsibilities apply for the Senior Supplier Engineering Manager. This includes, but is not limited to the following: Functional manager for a team of supplier quality engineers and contractors ensuring portfolio execution in NPD. Provide timely and constructive feedback on job performance and manage career development. Ensure the PVH Supplier quality processes are efficient and compliant. Drive Design for Reliability and Manufacturability (DRM) principles/process at suppliers Support for regulatory submission preparation, and internal and external auditsMUST HAVE - MINIMUM REQUIREMENTS:TO BE CONSIDERED FOR THIS ROLE, PLEASE BE SURE THE MINIMUM REQUIREMENTS ARE EVIDENT ON YOUR RESUME Bachelor's degree in Engineering, Science, or a technical discipline Minimum of 7 years of work experience in Engineering, Science, with 5 years of managerial experience, OR Advanced degree in Engineering, Science, or technical discipline with 5 years of managerial experience.Nice to Have Experience in Supplier Quality Engineering, Design Assurance Engineering &/or Research and Development in a regulated environment. Demonstrated ability to successfully provide technical direction and communicate technical risks and opportunities within areas of limited information. Able to solve complex problems that require creativity. Ability to perform well in cross-functional development teams. Experience with improvement tools preferred: six sigma, lean manufacturing, and theory of constraintsAbout 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. Lets 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 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. Learn more about our benefits here (https://www3.benefitsolver.com/benefits/BenefitSolverView?page_name=signon&co_num=30601&co_affid=medtronic) .This position is eligible for a short-term incentive plan. Learn more about Medtronic Incentive Plan (MIP) here .The provided base salary range is used nationally (except in certain CA locations).The rate offered is compliant with federal/local regulations and may vary by experience,certification/education, market conditions, location, etc.Base pay is based on numerous factors and may vary depending on job-relatedknowledge, skills, and experience.Min Salary150800Max Salary226200It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.#J-18808-Ljbffrby Jobble

Engineering ManagerCareers that Change LivesWe value what makes you unique. Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology 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. Be a part of a company that thinks differently to solve problems, make progress, and deliver meaningful innovations.In this exciting role as an Engineering Manager, you will have responsibility for managing the post-market quality operations for the Mechanical Circulatory Support Operating Unit (MCS OU). This role leads the reliability engineering team. The Engineering Manager directly contributes to patient safety by managing quality issue resolution including managing relationships with our customers and regulators for the MCS product portfolio. This role partners closely with design, manufacturing operations quality and supplier quality teams. The Engineering Manager also plays a key role in strategy and planning for the MCS OU.The Mechanical Circulatory Support Operating Unit is responsible for Medtronics heart pump program. Called the HeartWare HVAD System, this business provides a left ventricular assist device (LVAD) that helps patients hearts pump and increases the amount of blood that circulates through their bodies. The HVAD System features the world's smallest, commercially available, centrifugal flow pump.This position is in Mounds View, MN. within the Mechanical Circulatory Support (MCS) operating unit and requires on-site presence three days a week.We believe that when people from different cultures, genders, and points of view come together, innovation is the result and everyone wins. Medtronic walks the walk, creating an inclusive culture where you can thrive.A Day in the LifeIn general, the following responsibilities apply for the E ngineering Manager role. This includes, but is not limited to the following: Oversees risk assessments and product risk management files. Includes decision making on product holds and managing field corrective actions where appropriate. Selects, develops and evaluates personnel to ensure the efficient operation of the function. Leads capacity planning for reliability engineering resources in collaboration with PMO team. Leads post-market strategy for the MCS OU including direct engagement with OU senior staff and the MCS Independent Practitioner Quality Panel. Serves as the voice of quality engineering on the MCS CAPA Board. Regularly interfaces with US FDA and global regulators to communicate post-market strategy, respond to MDR and Part 806 questions, and ensure timely responses to requests for additional information.Must Have: Minimum RequirementsTO BE CONSIDERED FOR THIS ROLE, PLEASE BE SURE THE MINIMUM REQUIREMENTS ARE EVIDENT ON YOUR RESUME Bachelors degree in Engineering, and/or Quality Minimum of 5 years of relevant experience in Engineering and/or Quality; managerial experience, OR advanced degree in Engineering, and/or Quality with a minimum of 3 years of relevant experience with 3 years of managerial experienceNice to Have Front-room and back-room FDA audit experience. Experience in manufacturing a Class III active implantable medical device. Pre or post market quality experience with risk assessments and/or risk management files. Experience responding to audit observations and resolution of Warning Letter or other regulatory enforcement actions. Experience in the execution of field corrective actions Experience in Manufacturing engineering and/or manufacturing quality engineeringAbout 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. Lets 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 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. Learn more about our benefits here (https://www3.benefitsolver.com/benefits/BenefitSolverView?page_name=signon&co_num=30601&co_affid=medtronic) .This position is eligible for a short-term incentive plan. Learn more about Medtronic Incentive Plan (MIP) here .The provided base salary range is used nationally (except in certain CA locations).The rate offered is compliant with federal/local regulations and may vary by experience,certification/education, market conditions, location, etc.Base pay is based on numerous factors and may vary depending on job-relatedknowledge, skills, and experience.Min Salary128400Max Salary192600It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.#J-18808-Ljbffrby Jobble

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Engineering Manager Medtronic Jobs

Engineering Manager Software Design Quality Embedded ProductsApril 28, 2024

Senior Engineering Manager Plymouth MnApril 28, 2024

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Engineering Manager Mounds View MnApril 25, 2024

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