Senior Product Engineer
| Company | Medtronic |
|---|---|
| Location | Boston, MA, USA, North Haven, CT, USA |
| Salary | $102400 – $153600 |
| Type | Full-Time |
| Degrees | Bachelor’s |
| Experience Level | Senior |
Requirements
- Bachelor’s degree with 4+ years of engineering experience
- An advanced degree with 2+ years of engineering experience
Responsibilities
- Communicate with internal & external stakeholders, and those interactions will influence product roadmap prioritization and identifying the appropriate timelines to influence meaningful change.
- 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.
- May assist customer in device usage problems or customer testing of complex devices.
Preferred Qualifications
- 5-7 years of medical device engineering experience
- Experience with a large company with a global footprint, understanding of matrix structures, and having project management experience executing goals with cross functional teams using Agile/Scrum/SAFe methodologies.
- Thorough understanding of SW product development life cycle/process.
- Understanding the role of a Product owner using an Agile environment.
- Experience building and prioritizing backlogs.
- Understanding of the change development process (CDP) for implementing small-med-large projects.
- Understanding/experience with executing corrective and preventative actions (CAPA) and championing cause-map activities with broad cross-functional teams.
- Medical product development experience including hands-on experience with medical/surgical devices/instruments; familiarity with medical device regulations including IEC 62304.
- Experience SDLC process and tools including JIRA, JAMA, and AGILE PLM/PQM.
- 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.