Principal R&D Engineer
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 Principal R&D Engineer, you will develop life-saving medical device products for spine surgery. Key responsibilities include collaborating with a team to lead new product development, creating and designing implants, instruments, and systems, conducting product and use testing, and managing system interfaces. You will actively seek Voice of the Customer (VOC) input and translate that into product requirements, design specifications, and mechanical concepts. You will work under general direction and may serve as a key functional core team member or as an engineer on an extended team. The product focus will be on spinal implants and instrumentation to treat degenerative, deformity, and tumor / trauma conditions.
A career at Medtronic is like no other. We're purposeful. We're committed. We're driven by our Mission to alleviate pain, restore health, and extend life for millions of people worldwide. We seek out and hire a diverse workforce at every level : We need fresh ideas and inclusive insights to continue to be an innovative industry leader that's why we make it a point to seek out, attract, and develop employees who are patient-centric, passionate, and who represent the same wide variety of life experiences as our patients.
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 :
- Plans and implements all aspects of multiple simultaneous designs and development of new medical device products from initial design to market release following agreed project timelines and NPI Development processes.
- Defines medium to high complexity spinal systems and conceptualizes designs that meet the needs and uses of the customer, regulatory agencies, and the business under the guidance of the NPI Engineering Program manager and the Therapy Technical Leader.
- Provides technical leadership in the definition, evaluation, and mitigation of risk of system designs. This includes understanding system interfaces, use cases, and conditions, investigating and resolving system and design issues, making improvements to address customer feedback and requests, and leading testing activities.
- Engages with customers (internal and external) to understand and prioritize their needs and apply feedback to improve designs
- Translates customer needs into stakeholder and system requirements
- Optimizes designs by designing and conducting relevant tests, experiments, and evaluations, including numerical verification
- Defines and performs verification and validation activities, ensuring products meet user needs, system requirements, and intended use
- Writes engineering reports and creates presentations as required to document and communicate results
- Contributes and builds domain knowledge around spinal systems, their clinical use, and application via customer and field visits, pre-clinical in vivo labs, literature searches, and training
- Documents tradeoffs, rationales, and potential solutions
- Supports documentation throughout all phases of research and development
- Participate with outside suppliers and consultants to ensure timely delivery
- Investigate and evaluate existing technologies
- Contributes inventions, new designs, and techniques regarded as advances in the medical and technical / scientific community
- Provides training and mentorship to less experienced team members and learns from more experienced team members
- Maintains training and ensures personal understanding of all applicable quality policy / system items. Follow all work / quality procedures to ensure quality system compliance and high-quality work.
Travel Expectation : less than 10% - domestic travel 1 to 2 days a month.
As a Principal R&D Engineer :
Demonstrated strong performance in both what and how over time and career aspirations to advanceValues knowledge transfer and development and actively mentor othersDeep domain technology expertAbility to establish the link between technology and business / patient applicationStrong internal influence, collaboration & results within the organization and or locationsMust Have : Minimum Qualifications
Bachelor's degree in engineering or technical-related degree Mechanical Engineering preferredMinimum of 7 years of engineering design and development experience or advanced degree with a minimum of 5 years of medical device experience - in spine, trauma, orthopedics, or dentalNice to Have :
Engineering MS degree preferredClinical knowledge for uses of productsKnowledge of spinal anatomy relative to surgical proceduresExperience in the use of systems engineering methodologies, including requirements development, analysis, allocation, review, tracing, and verification / validationAbility to effectively communicate and work collaboratively with others as a member of a teamIn-depth knowledge and wide application of technical principles, theories, and concepts in related fields of expertise to develop innovative approaches to workKnowledge of manufacturing processes, including machining and 3D printingUnderstanding of spinal medical device industry and competitor products. Working knowledge of other disciplines.Skills & Abilities :
Proven proficiency with CREO, SolidWorks, or similar 3D CAD programMastering of engineering drawing standards, including GD&T and tolerance stacksDemonstrated track record of successful designs of surgical instruments (Spinal instruments are a plus)Knowledge of Agile and WindchillDemonstrated ability to take initiative in keeping current with technology developments in specialized areaExperience working in an FDA-regulated and / or medical device environment with ISO and Quality System Regulation requirementsDesign and project execution agility in a fast-paced environment with a quality and customer service mindset, along with a sense of urgency and ownershipCreativity in design, documentation, and problem-solving with speed as a priorityCapability to define and follow priority with multiple simultaneous projectsKnowledge of surgical instruments use conditions and OR setup (Spine is a plus)Strong collaborator in a cross-functional and multi-cultural team environmentStrong team player aiming to win as a teamStrong analytical and problem-solving skillsExperience training and mentoring less experienced engineers, learning / listening mindset with more experienced team membersExcellent written and communication skillsPhysical 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) : $130,400.00 - $195,600.00 This 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