Product Engineer II- VAVE (Manufacturing/R&D).
New Yesterday
Senior Product Engineer
Hybrid Remote Model: Onsite in Minneapolis 3x week hybrid model
Travel up to 20% domestically and internationally
Medtronic
At Medtronic, we value what makes you unique. Be part of a company that thinks differently to solve problems, make progress and deliver meaningful innovations
Our Purpose
At our Value Analysis/Value Engineering (VAVE) group in Medtronic, plc, we support value engineering activities for commercialized products and new products. The ideal candidate will have a design mindset that will improve devices in terms of cost, manufacturability, and ease of clinical use. The Engineer will be involved in the forefront of technology and innovation to bring ideas to fruition.
Come for a job, stay for a career!
A Day in The Life:
To be successful in this role, a mix of prior manufacturing and R&D experience is preferred.
Perform product design and development, specializing in improving the value of legacy products.
Work independently on product tear downs and functional analysis with minimal oversight.
Coordinate and support value engineering events with various cross-functional groups.
Key participant in DFMEA, PFMEA, and CTQ processes assuring proposed changes do not impact the device.
Lead cross-functional and/or departmental groups to develop and provide design recommendations that integrate into components or products with moderate complexity.
Interface with R&D, Customers, Marketing, Manufacturing and Suppliers to discover and trial new raw materials or production processes with the intent of improving performance or quality, reducing cost, and improving manufacturing efficiencies.
Keep current with technology/engineering advances to deliver best available technology to the project.
Effectively manage projects, coordinate activities and communicate progress to key stakeholders.
Partner with Medtronic’s supply base to create and evaluate potential value improvement opportunities.
Communicate technically with key stakeholders and develop product and process expertise and complete activities per compliance requirements.
Create project proposals to present business case to leaders.
Continue to enhance engineering and leadership skills through additional training and education.
Must Have: Minimum Requirements
Bachelors degree required
Minimum of 2 years of relevant experience, or advanced degree with 0 years of experience
Nice to Have
Medical Device Experience, preferably with implantables
Electrical engineering or medical device background
Ability to work independently and manage time well
Team player - ability to effectively interact with all disciplines
Self-starter - ability to interpret critical aspects of information received from multiple sources
Dynamic, positive attitude
Strong communication and drive for results
Solid design, troubleshooting and presentation skills
SolidWorks, Office Suite, Minitab
Knowledge of FDA Quality Systems Regulations and ISO Quality Systems
Working knowledge of Six Sigma
Working knowledge of GD&T
Good project management capabilities with experience in medical process validations preferred
- Location:
- Minneapolis