Senior Principal Development Engineer
Medtronic
- Boston, MA North Haven, CT
- Permanent
- Full-time
- Review and provide input to the development of product requirements
- Review, provide input to and approve test methods
- Design studies and experiments to gain confidence in meeting product requirements
- Analyze test data
- Author Engineering Analyses and Reports
- Plan verification activities
- Author Design Verification Protocols and Reports
- Troubleshoot failures and make recommendations on design, test, or requirement improvements
- Mentor junior engineers on all of the above
- Champion continuous improvement projects, such as implementing new SOPs or WIs related to development engineering
- Develop and drive a robust and efficient Design Verification strategy for product requirements
- Author or review/approve Design Verification protocols and reports
- Champion studies and/or activities that drive robust design, such as design of experiments, transfer function development, and simulations
- Lead cross-functional failure investigations and analysis
- Partner with System Engineering to develop, review and decompose product requirements
- Represent the development engineering function on product development extended core teams
- Mentor junior and senior development engineers working on your projects, and provide feedback on engineering reports, verification protocols, and verification reports
- Liaison with Reliability, Compliance (60601), Hardware (Electrical and Mechanical), and Software teams for your projects
- Support the development of regulatory submissions for your projects
- Support QMS and/or DHF audits as the development engineer SME on those projects
- Support changes made to your projects post-launch
- Performs technical planning, system integration, verification and validation, evaluates alternatives including cost and risk, supportability and analyses for total systems.
- Analyses are performed at all levels of total system product to include: concept, design, fabrication, test, installation, operation, maintenance and disposal.
Nice to Have
- 8+ years of medical device development
- Advanced degree in robotic engineering or another technical discipline
- Industry experience with statistical methods and analysis of data to perform Design Verification
- Experience with developing a product according to System Engineering principles
- A strong understanding of Regulatory requirements for Design Controls and Design Verification
- Industry-experience with statistical analysis of data
- Experience with robotics or electro-mechanical systems
- Proven track record of contributing to medical devices of high complexity
- Strong communication and inter-personal skills
- Posting Date: Apr 30, 2024
- Travel: Yes,
- Salary Min: 147200
- Salary Max: 220800