Medtronic
Sr Principal Mechanical Design Engineer
Medtronic, Los Angeles, California, United States, 90079
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Sr Principal Mechanical Design Engineer
role at
Medtronic We anticipate the application window for this opening will close on - 17 Oct 2025
At 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
As a member of the Mechanical Engineering R&D group, the individual selected for this role will lead new product development activities of products such as insulin pumps, glucose sensors, and related accessories. They will work at the intersection of product design and product development, optimizing customer and business needs. The ideal candidate for this position has the following: extensive experience in new product and process development, design and process characterization, process validation and design verification testing, experience in plastics and electromechanical assemblies in the medical device industry a plus, background in process design, development and qualifications including Test Method Validation (TMV) as well as hands-on prototyping/testing. This individual is experienced in problem solving and performing data analysis using statistical methods and tools (DOE, Regression, ANOVA, Capability Analysis, GR&R). Self-Starter and a technical leader with a sharp focus on quality and customer experience. This position will work across the organization driving and collaborating with functions in R&D, Operations, PMO, Quality and Regulatory to assure the successful execution of business goals. We are dedicated to making sure that every patient gets the best product — when they need it. We have strong ties to our local communities. Our vibrant employee communities respect and value individual experience and perspective as we aim to improve lives and access to healthcare. This position is an exciting opportunity to work with Medtronic's Diabetes business. Medtronic has announced its intention to separate the Diabetes division to promote future growth and innovation within the business and reallocate investments and resources across Medtronic, subject to applicable information and consultation requirements. This separation provides our team with a bold opportunity to unleash our potential, enabling us to operate with greater speed and agility. As a separate entity, we anticipate leveraging increased investments to drive meaningful innovation and enhance our impact on patient care. Job duties to be primarily located on-site in Northridge, CA with the ability to work limited hours remotely. Responsibilities may include the following and other duties may be assigned. Drive and lead product and process development activities of complex medical products by identifying key process inputs, outputs, controls, and noise factors by effective utilization of Six Sigma tools Drive and lead design transfer activities ensure that products are transitioned to manufacturing facility successfully Apply methodologies such as Design for Reliability and Manufacturing (DRM), Design for Six Sigma (DFSS), Design for Manufacturing Assembly / Automation (DFM/A) during process design and development phase Lead and perform process characterization, design verification / testing, and Test Method Validation (TMV) activities Perform Statistical analysis (DOE, Regression, ANOVA, Capability Analysis, GR&R) Help with equipment selection, tooling and fixture development, procurement, installation, and qualification. Drive corrective and preventive actions with appropriate and detailed follow-up Provide guidance and mentorship to junior engineering staff Help develop specifications, test methodologies, and test equipment to evaluate design concepts Perform calculations, analyses, and engineering testing to verify the designs and design changes. Document results in engineering reports and laboratory notebooks Works closely with strategic partners and vendors to support current products and initiate new production projects and assists in developing processes/techniques to meet contract objectives Help ensure designs meet and exceed product specifications, regulatory requirements, and international standards Design / develop components to be manufactured via plastic injection molding, stamping, machining, extrusion, and related processes Work with manufacturing to ensure feasibility of high-volume assembly in early phase of development cycle Translate voice of customer (VOC) feedback into engineering requirements Work with suppliers to ensure components meet design requirements & diagnose design / process problems Present technical findings or project status to cross functional teams and management through meeting minutes, design reviews, presentations, and other means of communication. Travel to supplier and manufacturing sites as required Must Have: Minimum Requirements
To be considered for this role, please ensure the minimum requirements are evident on your resume.
Bachelor of Engineering degree and 10+ years of experience in mechanical product and process development OR Master's degree with a minimum of 8 years relevant experience OR PhD with 6 years relevant experience Nice to Have:
Experience designing and developing electromechanical assemblies (Drug Delivery Systems or Continuous Glucose Sensors) Formal training in Six Sigma methodologies Experience with high-volume manufacturing Understanding of medical device design controls; lead design reviews and ensure on-time completion of Design Control deliverables Working knowledge of ISO 13485, ISO 14971, 21 CFR 820, IEC 62304, IEC 60601-1, MDD & EU MDR. 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. 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):$157,600.00 - $236,400.00 This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP). About Medtronic
Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people. We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary. It 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.
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Sr Principal Mechanical Design Engineer
role at
Medtronic We anticipate the application window for this opening will close on - 17 Oct 2025
At 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
As a member of the Mechanical Engineering R&D group, the individual selected for this role will lead new product development activities of products such as insulin pumps, glucose sensors, and related accessories. They will work at the intersection of product design and product development, optimizing customer and business needs. The ideal candidate for this position has the following: extensive experience in new product and process development, design and process characterization, process validation and design verification testing, experience in plastics and electromechanical assemblies in the medical device industry a plus, background in process design, development and qualifications including Test Method Validation (TMV) as well as hands-on prototyping/testing. This individual is experienced in problem solving and performing data analysis using statistical methods and tools (DOE, Regression, ANOVA, Capability Analysis, GR&R). Self-Starter and a technical leader with a sharp focus on quality and customer experience. This position will work across the organization driving and collaborating with functions in R&D, Operations, PMO, Quality and Regulatory to assure the successful execution of business goals. We are dedicated to making sure that every patient gets the best product — when they need it. We have strong ties to our local communities. Our vibrant employee communities respect and value individual experience and perspective as we aim to improve lives and access to healthcare. This position is an exciting opportunity to work with Medtronic's Diabetes business. Medtronic has announced its intention to separate the Diabetes division to promote future growth and innovation within the business and reallocate investments and resources across Medtronic, subject to applicable information and consultation requirements. This separation provides our team with a bold opportunity to unleash our potential, enabling us to operate with greater speed and agility. As a separate entity, we anticipate leveraging increased investments to drive meaningful innovation and enhance our impact on patient care. Job duties to be primarily located on-site in Northridge, CA with the ability to work limited hours remotely. Responsibilities may include the following and other duties may be assigned. Drive and lead product and process development activities of complex medical products by identifying key process inputs, outputs, controls, and noise factors by effective utilization of Six Sigma tools Drive and lead design transfer activities ensure that products are transitioned to manufacturing facility successfully Apply methodologies such as Design for Reliability and Manufacturing (DRM), Design for Six Sigma (DFSS), Design for Manufacturing Assembly / Automation (DFM/A) during process design and development phase Lead and perform process characterization, design verification / testing, and Test Method Validation (TMV) activities Perform Statistical analysis (DOE, Regression, ANOVA, Capability Analysis, GR&R) Help with equipment selection, tooling and fixture development, procurement, installation, and qualification. Drive corrective and preventive actions with appropriate and detailed follow-up Provide guidance and mentorship to junior engineering staff Help develop specifications, test methodologies, and test equipment to evaluate design concepts Perform calculations, analyses, and engineering testing to verify the designs and design changes. Document results in engineering reports and laboratory notebooks Works closely with strategic partners and vendors to support current products and initiate new production projects and assists in developing processes/techniques to meet contract objectives Help ensure designs meet and exceed product specifications, regulatory requirements, and international standards Design / develop components to be manufactured via plastic injection molding, stamping, machining, extrusion, and related processes Work with manufacturing to ensure feasibility of high-volume assembly in early phase of development cycle Translate voice of customer (VOC) feedback into engineering requirements Work with suppliers to ensure components meet design requirements & diagnose design / process problems Present technical findings or project status to cross functional teams and management through meeting minutes, design reviews, presentations, and other means of communication. Travel to supplier and manufacturing sites as required Must Have: Minimum Requirements
To be considered for this role, please ensure the minimum requirements are evident on your resume.
Bachelor of Engineering degree and 10+ years of experience in mechanical product and process development OR Master's degree with a minimum of 8 years relevant experience OR PhD with 6 years relevant experience Nice to Have:
Experience designing and developing electromechanical assemblies (Drug Delivery Systems or Continuous Glucose Sensors) Formal training in Six Sigma methodologies Experience with high-volume manufacturing Understanding of medical device design controls; lead design reviews and ensure on-time completion of Design Control deliverables Working knowledge of ISO 13485, ISO 14971, 21 CFR 820, IEC 62304, IEC 60601-1, MDD & EU MDR. 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. 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):$157,600.00 - $236,400.00 This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP). About Medtronic
Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people. We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary. It 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.
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