Manufacturing/Mechanical Salary in North Haven, CT

Careers that Change Lives / Impact patient outcomes/ come for a job, stay for a career.You will join Medtronic's Surgical Innovations Manufacturing team located in our North Haven, CT manufacturing facility.We are the global pioneer of advanced surgical instruments. Together, we deliver intelligent solutions, inspiring confidence in surgeons to enhance patient outcomes today and tomorrow.We reward you in the ways that matter most to you. We offer a wide range of benefits and rewards programs to recognize the important role you play in our Mission to transform healthcare. To learn more, we invite you to visit benefits.medtronic.comA Day in the LifeResponsibilities may include the following and other duties may be assigned. Performs a variety of tasks ranging from repetitive to non-repetitive production assembly operations. Works from visual aids, method layouts, diagrams, schematics, process flow sheets and written or verbal assembly instructions. Sets initial layouts, and uses a variety of tools to prepare product(s). Makes continuity checks on work in process and completed. May conduct quality inspections on processing line in accordance with quality specifications. May disassemble, modify, rework, reassemble, and test experimental or prototype assemblies and subassemblies according to specifications and under simulated conditions. Must Have: Minimum Requirements 0 years of experience required 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 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 .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.

Senior Product Engineer, R&D RPE - Robotic Surgical TechnologiesThis position will be based out of Medtronic's campus in North Haven, CT and reports to the Engineering Manager of the Capital Product Engineering Team in Released Product Engineering Organization. The Senior Product Engineer will coordinate the cross-functional team to deliver hardware design changes for products used for Robotic Surgery Hugo.Outstanding written and verbal communication skills are critical to success in this role, as is the ability to thrive in a fast-paced environment. You will work closely with mechanical, electrical and verification engineering teams to plan the technical details of the hardware change, while coordinating with project management, manufacturing, marketing and quality to meet timelines and business needs. This person will be able to dive in deep technically, but also able to see the broader needs of the business and the Robotics Surgical Technologies business unit.Location: North Haven, CTOperating UnitIn the Robotic Surgical Technologies, part of Medtronic's Surgical Operating Unit, we believe patients around the world deserve access to quality care and improved outcomes. We strive to expand global access to care and reduce variability through robotic and analytics solutions.You will join a world class team of mechanical, electrical and software engineers responsible for further development and enhancement of the globally launched Robotic Assisted Surgery platform: https://www.medtronic.com/covidien/en-us/robotic-assisted-surgery/hugo-ras-system.htmlCareers that Change LivesOne of the many ways we foster our inclusive environment is through our Diversity Networks and Employee Resource Groups. Our Diversity Networks leaders are teams appointed by our CEO. They champion programs and policies that advance more women and ethnically diverse employees into leadership roles. In the U.S., we have an African Descent Network, Asian Descent Network and Hispanic Descent Network. The PRIDE network and the Medtronic Women's Network are global communities. These unique networks are critical to ensuring the voice of the community is heard. They work closely with senior leaders and HR to create programs to further the advancement of diverse employees.A Day in the Life Lead cross functional team to drive execution of hardware design changes or enhancements proposed for Hugo Capital Product. Be the key central communications point for sustaining related project activity. Track deliverables from internal and external teams against product design change requirements. Anticipate, identify, and provide technical solutions to a wide range of difficult problems. Understand root cause analysis tools with ability to participate in investigations leading to problem resolution. Mitigate production and manufacturing risks by identifying areas of opportunity and executing improvement projects. Ability to drive technical changes related to product component & assembly, with knowledge of process and finished product impact. Assess timeline impacts against project schedule. Work with engineers to develop a deep understanding of the technological underpinnings of the system. Conducts project management tasks & documentation with design controls and risk analysis in accordance with established SOPs. Lead or coordinate with peers on product investigations that drive design and process improvement efforts. Participate in new process development activities at supplier base and contract sites, along with qualification efforts to implement new product materials or process changes. Incorporate required regulatory standards (FDA, ISO) in developmental and/or sustaining engineering projects including written protocols, test methods, assembly processes and the Design History File. Prepare reports, presentations and spreadsheets of an analytical and interpretative nature using statistical data analysis methods. Responsible for production support engineering with respect to testing methods, procedures, and problems; device specification and yield problems; minor redesign of devices and masks; analysis of customer returns; supplier related engineering changes and optimizing device production relative to cost constraints. Assumes responsibility for device and/or internally produced or externally purchased components after transfer into high-volume production and usually responsible for entire device manufacturing operations other than wafer fabrication. Additional tasks as assigned Must Have: Minimum Requirements Bachelor's degree with 4+ years of engineering experience OR An advanced degree with 2+ years of engineering experience Nice to Have 5+ years of medical device experience Advanced degree in engineering Experience with medical device hardware design changes Experience with robotic devices Strong leadership skills Knowledge of medical device manufacturing documentation for product release Knowledge of project management tools Outstanding verbal and written communication skills Comfortable working in a fast paced, cross disciplinary environment Ability to discuss technical details with engineering staff, the ideal candidate will have a strong engineering and product development background. Able to work with minimal direction towards completing project tasks Takes initiative in keeping current with technology developments in specialized area. Working knowledge of applicable FDA and ISO standards. Thorough understanding of engineering practices, product safety and root cause analysis. Working knowledge of Design for Six Sigma, Failure Mode Effects Analysis, Statistical Analysis methods, and Design of Experiments. Effective in written and oral communication; experienced in report writing and development of presentations. Good understanding of structured product development (requirements-driven engineering, documentation, rigorous verification, etc.) Engineering verification test development and execution Understanding and experience with system reliability testing and service. 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)CompensationA 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 .This position is eligible for a short-term incentive plan. Learn more about Medtronic Incentive Plan (MIP) on page 6 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.

Senior Mechanical Design Engineer - Robotic Surgical Technologies Released Product Engineering -North Haven, CT or Boston, MAThe Senior Mechanical Design Engineer is a primary contributor within the Medtronic R&D released product engineering (RPE) team to support released Robotic Instrumentation & Consumables for Medtronic's Robotic Surgery Technology platform.This Senior Mechanical Design Engineer is a key contributor in a fast-paced environment, working within a team to deliver advanced technical expertise and solutions to complex engineering problems.Working Conditions Standard office setting, surgical lab, pilot lab, external research organizations, supplier visits, limited travel as required. Based in North Haven, CT or Boston, MA / not open to remote candidates. Careers that Change LivesYou will be a key member of the Medtronic Engineering team responsible for developing Medtronic's Robotic Assisted Surgery platform through commercial launch and production scale-up, impacting patient outcomes.The Medical Surgical Group strives to enable earlier diagnosis, better treatment, faster complication-free recovery, and enhanced patient outcomes through less invasive surgical solutions. The Surgical Operating Unit sets the standard for Minimally Invasive Surgery (MIS) by creating innovative surgical products and services.Day in the Life Acting as first point of contact for Released Product Engineering in order to: Provide rapid response for line-down issues. Coordinate between R&D subject matter experts and other Released Product Engineering counterparts. Maintain electromechanical products and capital medical equipment. Participate in hardware deliverables of the Change Development Process for capital medical equipment. Determine change impact on mechanical/electromechanical design and document rationales Maintain bill of materials using product lifecycle management software (Agile) Perform kinematic and structural analyses to evaluate product performance and safety Compose engineering drawings, reports and presentations to document and communicate design deliverables and analyses Collaborate with the Medtronic R&D new product development engineering team who will be responsible for designing, developing, and supporting the next generation of capital equipment for the minimally invasive surgical robotic platform. Interact and negotiate with contract manufacturers, suppliers, and external partners Provide guidance, coaching and mentoring to junior members of the team Researches, plans, designs, verifies, validates and develops mechanical and/or electromechanical products and systems, such as metals, instruments, controls, plastics, robots, engines, machines and mechanical, resonance, hydraulic or heat transfer systems for production, transmission, measurement, and use of energy. Recommends various technology options or approaches for system, processes, facility or program improvements in terms of safety, performance, efficiency or costs. Additional tasks as assigned Must Have: Minimum Requirements Bachelor's Degree in Engineering, Science or technical field with 4+ years of engineering experience OR An advanced Degree in Engineering, Science or technical field with 2+ years of engineering experience Nice to Have 4+ years of mechanical design experience in medical device or another regulated industry Prior robotics experience Proficiency with Creo Parametric 3D Modeling Software and Windchill PLM Experience with Simulink and MATLAB Prior experience with pulley mechanisms, drive cables, gears, motors, sensor and complex electromechanical assemblies. Experience with Mechatronics. Understanding of common manufacturing processes (i.e. Injection Molding, Metal Forming, Machining, Heat Treating etc) Working knowledge of rapid prototyping, material selection, and product design and process specifications Ability to compile and organize technical data using Excel, Word, or Access. Trained/Certified in Lean and/or 6 Sigma Working knowledge of DFMEA and PFMEA Working knowledge of material handling principles 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)CompensationA 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 .This position is eligible for a short-term incentive plan. Learn more about Medtronic Incentive Plan (MIP) on page 6 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.

Careers that Change Lives 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. A Day in the Life The Manufacturing Engineer I is responsible for the direct support of assembly processes in North Haven, CT. This role will have responsibilities in troubleshooting equipment and driving down complex problems to find root cause and corrective actions. The products and processes vary in complexity and can contain both electric and mechanic interactions. This is also a hands-on role with immense satisfaction in improving outcomes of our patients through our production equipment. This Engineer will learn not only the assembly process but also the product and provide input on design changes and areas to improve the outcomes of our patients.Responsibilities may include the following and other duties may be assigned. Inspect performance of machinery, equipment, and tools to verify their efficiency, and investigate and initiate corrective action of problems and deficiencies to ensure product quality. Design ma nufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining, and material handling. Design arrangement of machines within plant facilities to ensure most efficient and productive layout. Design sequence of operations and specify procedures for the fabrication of tools and equipment and other functions that affect product performance. Adapt machine or equipment design to factory and production conditions. May incorporate inspection and test requirements into the production plan. Develop manufacturing processes that are applicable to statistical process control and may develop those techniques. Provide guidance to engineering regarding design concepts and specification requirements to best utilize equipment and manufacturing techniques. Ensure processes and procedures are in compliance with regulations. Support equipment validations and reports, including but not limited to IQ, OQ, PQ, & TMV. Must Have: Minimum Requirements Bachelors degree required 0 years of experience required Nice to Have • Bachelor's degree in engineering• Mechanical and/or Electrical aptitude• Creative thinking and problem solving• Communication skills in coordinating activities with cross functional groups 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.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 .The provided base salary range is used nationally in the United States (except in Puerto Rico and certain CA locations). The rate offered is compliant with federal/local regulations and may vary by experience, certification/education, market conditions, location, etc.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)

Careers that Change Lives 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. A Day in the Life The Senior Manufacturing Engineer is responsible for the direct support of assembly processes in North Haven, CT. This role will have responsibilities in troubleshooting equipment and driving down complex problems to find root cause and corrective actions. The products and processes vary in complexity and can contain both electric and mechanic interactions. This is also a hands-on role with immense satisfaction in improving outcomes of our patients through our production equipment. This Engineer will learn not only the assembly process but also the product and provide input on design changes and areas to improve the outcomes of our patients.Responsibilities may include the following and other duties may be assigned. Inspect performance of machinery, equipment, and tools to verify their efficiency, and investigate and initiate corrective action of problems and deficiencies to ensure product quality. Design manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining, and material handling. Design arrangement of machines within plant facilities to ensure most efficient and productive layout. Design sequence of operations and specify procedures for the fabrication of tools and equipment and other functions that affect product performance. Adapt machine or equipment design to factory and production conditions. May incorporate inspection and test requirements into the production plan. Develop manufacturing processes that are applicable to statistical process control and may develop those techniques. Provide guidance to engineering regarding design concepts and specification requirements to best utilize equipment and manufacturing techniques. Ensure processes and procedures are in compliance with regulations. Lead and execute equipment validations and reports, including but not limited to IQ, OQ, PQ, & TMV. Must Have: Minimum Requirements Bachelors degree required Minimum of 4 years of relevant experience, or advanced degree with a minimum of 2 years relevant experience Nice to Have • Bachelor's or master's degree in engineering• Formal training Six Sigma Root Cause Analysis• Mechanical and/or Electrical aptitude• Familiarity with manufacturing environments/assembly processes• Creative solutions and problem solving• Communication skills in coordinating activities with cross functional groups• Firm understanding of GD&T (Geometric Dimensioning and Tolerancing) 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.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 .The provided base salary range is used nationally in the United States (except in Puerto Rico and certain CA locations). The rate offered is compliant with federal/local regulations and may vary by experience, certification/education, market conditions, location, etc.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)

NO C2C Candidates, ONLY W2 Candidates pleaseBroad understanding of software validation techniques for medical or other regulated systems, you will develop a strong understanding of the SW architecture, design, and execute the test strategy, perform release activities of Software tests in compliance with regulatory standards.Bachelor's Degree required with minimum of 4 years of relevant experience, or advanced degree with a minimum of 2 years relevant experienceProvide software validation activities as part of the Software operations transfer team in the Software COE of Robotic Surgical Technologies.Lead definition and implementation of different software testing techniques to provide test coverage for the software used in manufacturing and service.Using software test engineering techniques to maximize validation coverage with optimal effort in both automation and manual testing.Develop and deliver all SW Validation deliverables for your project to support regulatory submission.Understand the technical behavior of the system, architecture, and software requirements with an aptitude to identify software defects in all phases of development.Coordination of dry runs and formal Validation activities as required.Collaborate with technical engineering teams, develop software tools when needed.Knowledge of Medical Product verification, IEC-62304, and FDA guidance.Understanding of creating test protocols for verifying software requirements.Strong understanding of good documentation practices.Ability to work with QA to ensure testing meets Quality and Regulatory needs.Ability to manage, track, and upgrade multiple hardware and software configurations.Ability to work with Systems, Mechanical, Electrical, and Software engineers when discovering, documenting, and resolving integration issues.Familiarity with common programming languages such as C++, C#, and Python.Experience using a tool or repository for managing test cases (GIT Stash, JIRA).

Broad understanding of software validation techniques for medical or other regulated systems, you will develop a strong understanding of the SW architecture, design, and execute the test strategy, perform release activities of Software tests in compliance with regulatory standards.Bachelor's Degree required with minimum of 4 years of relevant experience, or advanced degree with a minimum of 2 years relevant experienceProvide software validation activities as part of the Software operations transfer team in the Software COE of Robotic Surgical Technologies.Lead definition and implementation of different software testing techniques to provide test coverage for the software used in manufacturing and service.Using software test engineering techniques to maximize validation coverage with optimal effort in both automation and manual testing.Develop and deliver all SW Validation deliverables for your project to support regulatory submission.Understand the technical behavior of the system, architecture, and software requirements with an aptitude to identify software defects in all phases of development.Coordination of dry runs and formal Validation activities as required.Collaborate with technical engineering teams, develop software tools when needed.Knowledge of Medical Product verification, IEC-62304, and FDA guidance.Understanding of creating test protocols for verifying software requirements.Strong understanding of good documentation practices.Ability to work with QA to ensure testing meets Quality and Regulatory needs.Ability to manage, track, and upgrade multiple hardware and software configurations.Ability to work with Systems, Mechanical, Electrical, and Software engineers when discovering, documenting, and resolving integration issues.Familiarity with common programming languages such as C++, C#, and Python.Experience using a tool or repository for managing test cases (GIT Stash, JIRA).

Careers that Change LivesA Day in the LifeProvide comprehensive support to new product development teams with focus on supplier quality and design transfer activities.Responsibilities may include the following and other duties may be assigned. Works effectively with colleagues in cross-functional or departmental team projects Makes decisions and proposes solutions based on calculated risks identified through data analysis Leads or assists with part approval process activities to identify and qualify suppliers for critical instrument components while adhering to corporate policies and applicable regulations Implement approved changes using sound quality engineering principles and fully document them in compliance with Quality System Regulation (QSR 21 CFR 820), ISO 13485 and Corporate Policies. Assist with protocol and implement process validation procedures in accordance with QSR, FDA and international guidelines. Capable of leading cross-functional projects with little or no guidance. Coordinate activities through the Quality Engineering Manager and report regularly on the progress of activities. Participate in meeting departmental goals and objectives. Mentor or supervise junior engineers. Must Have: Minimum Requirements Bachelors degree required Minimum of 4 years of relevant experience, or advanced degree with a minimum of 2 years relevant experience Nice to Have Working knowledge of combination medical device products Effective verbal and written communication, analytical, influencing and interpersonal skills. Must be able to effectively communicate at all levels and across company lines as well as effectively communicate with suppliers. Six-Sigma greenbelt or blackbelt certification 5+ years of Quality Assurance experience in a QSR (GMP), disposable medical device environment Working knowledge of Quality System Regulation (QSR 21 CFR 820) and EU Medical Device Directive (EU MDD 93/42 EEC) Demonstrated working knowledge of manufacturing and supplier quality processes. PC skills, word processing, spreadsheets, project management, etc. 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 . This position is eligible for a short-term incentive plan. Learn more about Medtronic Incentive Plan (MIP) on page 6 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. 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)

Bring your talents to an industry leader in medical technology and healthcare solutions - we're a market leader and growing every day. You can be proud to part of technologies that are rooted in our long history of mission-driven innovation. You will be empowered to shape your own career. We support your growth with the training, mentorship, and guidance you need to own your future success. Together, we can transform healthcare.Join us for a career that changes lives. Careers That Change Lives A career at Medtronic is like no other. We're purposeful. We're committed. And we're driven by our Mission to alleviate pain, restore health and extend life for millions of people worldwide.In this exciting role as a Senior Quality Engineer you will have responsibility to provide support for product development programs for new medical device products for the Stapling platform. As an important member of our Quality Team, you will provide guidance and implement strategies that drive component quality, product quality and continuous improvement.A Day in the Life Responsibilities may include the following and other duties may be assigned. You will establish and successfully execute supplier management plans which will align to overall business objectives. Contribute to new product development through supplier selection, supplier qualification and establishing supplier controls. Develop and ensure proper execution of the Supplier Quality Strategy. Oversee the supplier non-conformance investigation, corrective action effectiveness and timeliness. Partner with Supply Chain to integrate strategies and ensure coordination and alignment across segmentation. Evaluates suppliers' internal functions to assess their overall performance and provides feedback in assessment of their operation. Monitors parts from acquisition through the manufacturing cycle and communicates unresolved supplier-related problems effectively in a timely manner. Participate in supplier performance review meetings and supplier training. Ensures that suppliers deliver quality parts, materials, and services. Qualifies suppliers according to company standards Drive the qualification of new product supplied material and ensure purchased products and components are manufactured and qualified in accordance with applicable industry standards, regulatory requirements, and customer requirements. Collaborates with cross-functional engineers 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. Participate in internal and external supplier audits Ensure documentation is completed per quality system procedures for supplier process development/validation and product qualification. Partners with R&D, Design Quality and Manufacturing Engineering to assist in developing test methods, equipment acquisition for new product testing, validations/qualifications, statistical analysis of data for significance, and other documented requirements for quality objectives. Must Have: Minimum Requirements Bachelors degree required Minimum of 4 years of relevant experience, or advanced degree with a minimum of 2 years relevant experience Nice to Have Master's degree in Engineering Lead auditor certification Proven ability to manage multiple priorities, drive projects to completion and meet internal customer expectations Strong written and oral communication and presentation skills Working knowledge of statistical data analysis May have broad knowledge of project management. Experience and working knowledge of FDA regulations/ISO standards for medical devices Strong interpersonal, organizational and project management skills Demonstrated skills in decision making Demonstrated ability in coaching/developing team members Strong interpersonal communication and influence skill Ability to work in a team-based environment Computer skills in MS Office and ERP systems desirable 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 . This position is eligible for a short-term incentive plan. Learn more about Medtronic Incentive Plan (MIP) on page 6 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. 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)

Careers that Change Lives 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.A Day in the Life The Manufacturing Engineer II is responsible for the direct support of assembly processes in North Haven, CT. This role will have responsibilities in troubleshooting equipment and driving down complex problems to find root cause and corrective actions. The products and processes vary in complexity and can contain both electric and mechanic interactions. This is also a hands-on role with immense satisfaction in improving outcomes of our patients through our production equipment. This Engineer will learn not only the assembly process but also the product and provide input on design changes and areas to improve the outcomes of our patients.Responsibilities may include the following and other duties may be assigned. Inspect performance of machinery, equipment, and tools to verify their efficiency, and investigate and initiate corrective action of problems and deficiencies to ensure product quality. Design manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining, and material handling. Design arrangement of machines within plant facilities to ensure most efficient and productive layout. Design sequence of operations and specify procedures for the fabrication of tools and equipment and other functions that affect product performance. Adapt machine or equipment design to factory and production conditions. May incorporate inspection and test requirements into the production plan. Develop manufacturing processes that are applicable to statistical process control and may develop those techniques. Provide guidance to engineering regarding design concepts and specification requirements to best utilize equipment and manufacturing techniques. Ensure processes and procedures are in compliance with regulations. Lead and execute equipment validations and reports, including but not limited to IQ, OQ, PQ, & TMV. Must Have: Minimum Requirements Bachelors degree required Minimum of 2 years of relevant experience, or advanced degree with 0 years of experience Nice to Have Bachelor's or master's degree in engineering Formal training Six Sigma Root Cause Analysis Mechanical and/or Electrical aptitude Familiarity with manufacturing environments/assembly processes Creative solutions and problem solving Communication skills in coordinating activities with cross functional groups Firm understanding of GD&T (Geometric Dimensioning and Tolerancing) 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.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 .The provided base salary range is used nationally in the United States (except in Puerto Rico and certain CA locations). The rate offered is compliant with federal/local regulations and may vary by experience, certification/education, market conditions, location, etc.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)