Advanced Product Engineer
13 hours ago
Job Description:
Advanced Product Engineer - Design Control
At Solventum, we are committed to delivering innovative solutions that improve lives. As a new company with a legacy of creating breakthrough products, we pioneer game-changing innovations at the intersection of health, material, and data science.
We partner closely with the brightest minds in healthcare to ensure that every solution we create melds the latest technology with compassion and empathy. Our team of experts is dedicated to driving improvement and delivering results.
The Impact You'll Make in this Role
As an Advanced Product Engineer, you will have the opportunity to collaborate with a diverse team of experts to drive innovation and improvement. Here, you will make an impact by:
- Leading efforts to improve the Design Control process.
- Ensuring alignment of the Design Control process across the global team.
- Identifying opportunities for more efficient uses of bench testing and/or modeling.
- Working with product teams to align design documentation with manufacturing specifications.
- Analyzing test data to understand correlations and identify redundancies.
- Writing standard operating procedures (SOPs) to clearly describe the Design Control process.
- Other duties as assigned.
Your Skills and Expertise
To set you up for success in this role from day one, Solventum requires (at a minimum) the following qualifications:
- Bachelor's degree or higher in a science or engineering discipline (completed and verified prior to start) from an accredited institution.
OR
- High School Diploma/GED AND four (4) combined years of engineering, manufacturing, and/or project management in a private, public, government or military environment
Additional qualifications that could help you succeed even further in this role include:
- Two (2) years of experience in one or more of the following areas: product engineering, product commercialization, product research and development, and/or manufacturing experience in the medical device industry
- Experience with the effective execution of change management, root cause analysis, issue resolution and/or managing corrective and preventative actions
- Experience writing design control documentation
- Medical device and/or Quality Management System (QMS) experience such as Food and Drug Administration (FDA) Quality System Regulation (QSR) and/or International Organization for Standardization (ISO) 13485
- Demonstrated experience utilizing project management techniques to lead cross functional teams in projects that drive improvement and proven results
- Experience collaborating with laboratory, quality and/or manufacturing colleagues in other regions of the world
- Experience with test method development, material property data collection and/or setting specifications and translating into product requirements
- Supporting complaint, plant non-conformance, and Supplier Corrective Action Request (SCAR) investigations, as well as external quality system and technical audits
- Statistical knowledge and practice e.g., Design of Experiments (DOE), sampling, Statistical Process Control (SPC), Product & Process Understanding (PPU), Lean manufacturing, etc.
Work location:
- Hybrid Eligible (Job Duties allow for some remote work but require travel to St. Paul, MN at least 2 days per week)
Travel: May include up to 10% domestic/international
Relocation Assistance: May be authorized
Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status).
Supporting Your Well-being
Solventum offers many programs to help you live your best life - both physically and financially. To ensure competitive pay and benefits, Solventum regularly benchmarks with other companies that are comparable in size and scope.
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