Ingeniero sénior de producto

## Ingénieur sr Produits Postuler:
Sur site:
North Haven, Connecticut, United States of America:
Temps plein:
Offre publiée aujourd'hui:
Date de fin : 2 novembre 2026 (Il reste 6 jour(s) pour postuler): R80180

We anticipate the application window for this opening will close on - 2 Nov 2026

Chez Medtronic, vous pouvez entamer une longue carrière d’exploration et d’innovation tout en aidant à soutenir l’accès aux soins de santé et l’équité pour tous. Vous dirigerez avec détermination en surmontant les obstacles à l’innovation dans un monde davantage connecté et compatissant.
** Journée type
** Team member responsible for Released Product Engineering (RPE) activities for surgical stapling devices. RPE is responsible for product design, Corrective Actions and Preventive Actions (CAPA) and product enhancements that ensure sustainability and improve clinical performance. Engineer will be expected to lead and/or champion initiatives from concept through implementation including presenting information/status of initiatives to management. Engineer would also be expected to provide leadership/mentorship to junior engineers.

Responsibilities may include the following and other duties may be assigned.
** Technical Functions*
* * Represents the organization in providing imaginative, thorough, practical solutions to difficult technical issues associated with specific products that are consistent with the organization’s objectives.
* Anticipates and identifies problems of a unique and challenging nature, including those requiring research and/or analysis to identify.
* Work on highly complex technical problems and provide solutions that are highly innovative and ingenious to a broad range of problems.
* Collaborate with peers to manage the development of appropriate testing to verify product meets internal and external customer requirements.
* Reviews and evaluates development protocols, results and conclusions.
* Demonstrates an understanding of functional and customer requirements.
* Collaborates with peers to develop appropriate testing to verify product meets requirements and sets appropriate specifications to ensure product reliability and manufacturability.
* Investigates customer complaints on existing products and helps to determine root cause of complaint and corrective actions if necessary.
* Incorporates required regulatory standards in developmental and/or sustaining engineering projects.
* Contributes inventions, new designs and techniques associated with the completion of specific projects.
* Provides primary technical contributions and or may lead sub projects.
* Adheres to safety policy and procedures.
** Project Management*
* * Conducts project management tasks and documentation with design controls and risk analysis in accordance with established SOPs.
* Prepares reports, presentations and spreadsheets of an analytical and interpretative nature to be presented to peers, executives, and customers.
** Must Have:

Minimum Requirements
*** Requires a Bachelor’s degree and minimum of 4 years of relevant experience, or advanced degree with 2 years of experience.
** Nice to Have*
* * Mechanical design experience
* Demonstrated ability to interpret a variety of technical information and deal with several abstract and concrete variables
* Knowledge and understanding of design change control process
* DRM, DFSS and/or Six Sigma training/experience
* Good communication and teamwork skills.
* Designs and redesigns medium-high complexity medical devices and subsystems.
* Tests and optimizes the design by conducting experiments and evaluations including numerical verification (finite element analysis (FEA), tolerance analysis etc.)
* Prepares documentation in accordance with relevant internal Standard Operating…