Medtronic is looking for an individual to help champion healthcare access and equity by designing, developing, and analyzing solutions within the field of life sciences and product development.
Requirements
- Designs, develops, analyzes, troubleshoots, and provides technical skills during research and/or product development.
- Designs studies to investigate specific life science questions within the field of expertise.
- Responsible for the design of components, sub-assembly products using PTC Creo.
- Develop and test prototypes from design specifications, define processes to properly make and assemble the product, and optimize the process.
- Coordinate various programs, which include FMEA (Failure Mode and Effects Analysis) and Risk Assessments.
- Coordinate Process Validation, DOE (Design of Experiments), Gage R&R (Gage Repeatability & Reproducibility), and GD&T (Geometric Dimensioning and Tolerancing).
- Utilize various failure investigation techniques, statistical quality control, protocol & report preparation, and non-conforming product controls.
Responsibilities
- Designs, develops, analyzes, troubleshoots, and provides technical skills during research and/or product development.
- Designs studies to investigate specific life science questions within the field of expertise.
- May be involved in product research and development and/or clinical trials.
- Translates research discoveries into usable and marketable products.
- Provide engineering support for new product design and development, including existing product modifications, process design, development, optimization, and performance evaluation.
- Defining requirements and system architecture for new product development for spinal instruments and implants.
- Responsible for the design of components, sub-assembly products using PTC Creo.
Other
- Requires a Baccalaureate degree
- Contributes towards planning and completion of deliverables through building relationships and consensus.
- Provide technical support for regulatory notifications and submissions using 510(k)s and PMAs for domestic and international approvals.
- 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.
