Thank you for your interest in joining Solventum. Solventum is a new healthcare company with a long legacy of solving big challenges that improve lives and help healthcare professionals perform at their best. At Solventum, people are at the heart of every innovation we pursue. Guided by empathy, insight, and clinical intelligence, we collaborate with the best minds in healthcare to address our customers’ toughest challenges. While we continue updating the Solventum Careers Page and applicant materials, some documents may still reflect legacy branding. Please note that all listed roles are Solventum positions, and our Privacy Policy: https://www.solventum.com/en-us/home/legal/website-privacy-statement/applicant-privacy/ applies to any personal information you submit. As it was with 3M, at Solventum all qualified applicants will receive consideration for employment without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Job Description: Material Reinvent Senior Quality Engineer 3M Health Care is now Solventum At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of creating breakthrough solutions for our customers’ toughest challenges, we pioneer game-changing innovations at the intersection of health, material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best. Because people, and their wellbeing, are at the heart of every scientific advancement we pursue. We partner closely with the brightest minds in healthcare to ensure that every solution we create melds the latest technology with compassion and empathy. Because at Solventum, we never stop solving for you. The Impact You’ll Make in this Role As a Material Reinvent Senior Quality Engineer you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by: Leading quality planning for critical material redesign or replacement projects for Solventum medical / combination devices. Ensuring critical to quality attributes are defined and achieved throughout the projects while maintaining compliance to our quality management system. Defining and implementing test methods and test method validation, stability, process validation, updated risk management files, supplier assessments, and material design verification and validation strategies to satisfy design change controls and ensure and improve reliability and capability, while continuing to meet our customers’ expectations of product performance and quality. Managing change through the lens of patient safety by assessing its impact on the products’ risk profile. Engaging cross-functional team to drive robust risk mitigations. Pursuing united goals with cross-functional global teams composed of members from R&D, manufacturing, regulatory, product stewardship, business, clinical, and various other functions. 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 (completed and verified prior to start) AND three (3) years of Medical Device, Pharmaceutical, or Combination Product experience in a Quality or Product Engineering or Design Assurance function in a private, public, government or military environment. Additional qualifications that could help you succeed even further in this role include: Experience and demonstrated scientific knowledge in the development of medical devices and in the application of regulations and standards relevant to medical device compliance, such as ISO 13485 and ISO 14971 Master’s degree in Chemistry, Biology/Microbiology, Materials Science, or a related discipline from an accredited institution American Society for Quality (ASQ) certification, such as Certified Quality Engineer (CQE) Experience and/or certification in Six Sigma methodologies related to the design and manufacture of new products Experience applying quality engineering and product development practices, including Design Controls (such as Design Verification), Process Validation, Risk Management, Test Method Validation, Critical‑to‑Quality (CTQ) definition and control, statistical data analysis, and continuous improvement, within highly technical and regulated environments Work location: Hybrid Eligible (Job Duties allow for some remote work but require travel to Eagan, MN) Travel: May include up to 20% 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
FULL TIME
senior
4/28/2026
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