Medtronic plc
We anticipate the application window for this opening will close on - 10 Oct 2025At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.# **A Day in the Life**Act boldly. Compete to win. Move with speed and decisiveness. Foster belonging. Deliver results…the right way. That’s the Medtronic Mindset — our cultural norms. Our brand is rooted in action, not just words. The Medtronic Mindset defines the expectations of our culture. Every person here plays a role in bringing it to life. We recognize your extraordinary potential to ensure future generations live better, healthier lives.As a member of Supplier Quality Engineering at Medtronic Energy and Component Center (MECC), you will be responsible for partnering with Development Engineering and Sourcing to identify, develop, qualify and release to manufacturing cost effective components/materials for use in Medtronic Cardiac Rhythm Management, Neuromodulation, Pelvic Health, or Surgical Innovations product. In this area of new product development, the Senior Supplier Quality Engineer will be required to drive multiple aspects of component/material development and approval with suppliers as a member of a cross-functional team.
Our Cardiac Rhythm Management Integrated Operating Unit offers devices and therapies that treat patients with abnormal heart rhythms and heart failure. It is comprised of four key businesses: Cardiac Pacing Therapies, Defibrillation Solutions, Patient Management, and Procedure Innovations. Together, we will transform the lives of people with cardiac arrhythmias and heart failure.At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We’re working a minimum of **4** days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary.Responsibilities may include the following and other duties may be assigned.* Ensure that suppliers deliver quality parts, materials, and services.* Partner with Technical Sourcing to locate, evaluate, and approve new potential component/material suppliers that balance business, quality, and technical requirements.* Provide Pre-Market Quality Engineering support to New Product Development (NPD) working in partnership with the Component Engineering and Post-Market Supplier Quality Teams, to deliver quality parts, materials, and services, prevent defects, and allow Medtronic to provide customers with the highest quality and reliable products.* Provide technical guidance and quality compliance for Supplier Quality engagement throughout the NPD lifecycle on newly qualified parts from NPD and implementing strategies for driving product quality and continuous improvement, ensuring purchased products and components are manufactured and qualified to Medtronic PPAP requirements.* Collaborate with Project Team to develop and deliver the Product Acceptance Sampling Strategy, Approved Supplier List coordination, Supplier Owned Quality deployment, and Control Plans for new products.* Define Receiving Inspection requirements as required and associated test method validation for all internal Medtronic Test Methods.* Work to develop proper inspection tooling and test methods for new components to ensure supplier parts meet specification requirements.* Perform statistical data analysis to determine tool and part/process performance. Evaluate Supplier capabilities for mechanical measurement via Gage R&R studies.* Ensure appropriate acceptance activities are in place prior to commercialization.* Plan, execute, and communicate own work and educating others on work products.* Provide regular, timely communication to manager and project team regarding status of assigned activities.* Metrology & Measurement; statistical analysis (Cpk, standard deviation, etc.), measurement uncertainty, GD&T, Gauge Repeatability & Reproducibility**Must Have: Minimum Requirements*****To be considered for this role, please ensure the minimum requirements are evident on your resume.**** Bachelors degree in engineering, science or technical field with 2+ years of experience in quality and/or engineering OR Advanced Degree in Engineering, Science or technical field with 0 years of experience in quality and/or engineering.**Nice to Have*** Working knowledge of ISO 13485, ISO 14971, 21CFR820* Experience in applying DMAIC / Lean Six Sigma principles; Green Belt certification* Good statistical data analysis skills, including SPC* Root cause analysis methodology* Risk Management or CAPA experience* Experience supporting New Product Development (NPD) projects, including collaboration within cross-functional project team structures* Experience in Automated Optical Inspection Validation* Excellent verbal and written communication skills* Ability to interface with internal customers, suppliers and external regulatory agencies* High attention to detail and accuracy* Medical device experience strongly preferred**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.# **Benefits & Compensation****Medtronic offers a competitive Salary and flexible Benefits Package**
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.Salary ranges for U.S (excl. PR) locations (USD):$77,600.00 - $116,400.00This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).## ## The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program). The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), #J-18808-Ljbffr
Our Cardiac Rhythm Management Integrated Operating Unit offers devices and therapies that treat patients with abnormal heart rhythms and heart failure. It is comprised of four key businesses: Cardiac Pacing Therapies, Defibrillation Solutions, Patient Management, and Procedure Innovations. Together, we will transform the lives of people with cardiac arrhythmias and heart failure.At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We’re working a minimum of **4** days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary.Responsibilities may include the following and other duties may be assigned.* Ensure that suppliers deliver quality parts, materials, and services.* Partner with Technical Sourcing to locate, evaluate, and approve new potential component/material suppliers that balance business, quality, and technical requirements.* Provide Pre-Market Quality Engineering support to New Product Development (NPD) working in partnership with the Component Engineering and Post-Market Supplier Quality Teams, to deliver quality parts, materials, and services, prevent defects, and allow Medtronic to provide customers with the highest quality and reliable products.* Provide technical guidance and quality compliance for Supplier Quality engagement throughout the NPD lifecycle on newly qualified parts from NPD and implementing strategies for driving product quality and continuous improvement, ensuring purchased products and components are manufactured and qualified to Medtronic PPAP requirements.* Collaborate with Project Team to develop and deliver the Product Acceptance Sampling Strategy, Approved Supplier List coordination, Supplier Owned Quality deployment, and Control Plans for new products.* Define Receiving Inspection requirements as required and associated test method validation for all internal Medtronic Test Methods.* Work to develop proper inspection tooling and test methods for new components to ensure supplier parts meet specification requirements.* Perform statistical data analysis to determine tool and part/process performance. Evaluate Supplier capabilities for mechanical measurement via Gage R&R studies.* Ensure appropriate acceptance activities are in place prior to commercialization.* Plan, execute, and communicate own work and educating others on work products.* Provide regular, timely communication to manager and project team regarding status of assigned activities.* Metrology & Measurement; statistical analysis (Cpk, standard deviation, etc.), measurement uncertainty, GD&T, Gauge Repeatability & Reproducibility**Must Have: Minimum Requirements*****To be considered for this role, please ensure the minimum requirements are evident on your resume.**** Bachelors degree in engineering, science or technical field with 2+ years of experience in quality and/or engineering OR Advanced Degree in Engineering, Science or technical field with 0 years of experience in quality and/or engineering.**Nice to Have*** Working knowledge of ISO 13485, ISO 14971, 21CFR820* Experience in applying DMAIC / Lean Six Sigma principles; Green Belt certification* Good statistical data analysis skills, including SPC* Root cause analysis methodology* Risk Management or CAPA experience* Experience supporting New Product Development (NPD) projects, including collaboration within cross-functional project team structures* Experience in Automated Optical Inspection Validation* Excellent verbal and written communication skills* Ability to interface with internal customers, suppliers and external regulatory agencies* High attention to detail and accuracy* Medical device experience strongly preferred**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.# **Benefits & Compensation****Medtronic offers a competitive Salary and flexible Benefits Package**
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.Salary ranges for U.S (excl. PR) locations (USD):$77,600.00 - $116,400.00This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).## ## The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program). The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), #J-18808-Ljbffr