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Senior Manager, R&D Design & Development – Chemical & Biological Systems

Job in Saint Paul, Dakota County, Minnesota, 55121, USA
Listing for: Solventum
Full Time position
Listed on 2026-08-05
Job specializations:
  • Engineering
    Regulatory Compliance Specialist
  • Management
    Regulatory Compliance Specialist
Job Description & How to Apply Below
Location: Saint Paul

Senior Manager, R&D Design & Development – Chemical & Biological Systems

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 Senior Manager, R&D Design & Development – Chemical & Biological, you will lead and partner with highly skilled engineers and scientists to deliver innovative medical device solutions that improve patient outcomes. You will collaborate across global, cross-functional teams and play a critical role in shaping the health, rigor, and future readiness of our IP&SS new product development portfolio.

R&D Leadership & Product Development

  • Lead and develop a high-performing team of Chemical and Biological R&D design engineers and scientists supporting the Vascular Access Solutions, Assurance & Monitoring Solutions, and Peri‑Operative Surgical Solutions portfolios.
  • Reduce program risk and uncertainty early by clearly defining scope and product requirements, aligning design capability, resources, and timelines, and identifying new capabilities or capacity needs (internal or external).
  • Drive the development of robust, reliable, and manufacturable component, subassembly, assembly, and system-level designs.
  • Partner closely with IP&SS R&D Product Development to ensure effective extended‑team resource allocation and delivery of committed program milestones.
  • Lead design controls, risk management, and documentation activities in compliance with medical device regulatory requirements.
  • Oversee product characterization, verification, and validation testing to ensure functional performance, safety, and design input compliance.
  • Continuously evaluate and mature designs to reduce cost, schedule, and technical risk while increasing confidence in business case achievement.
  • Enable smooth technology transfer to Sustaining Engineering as products enter commercialization and continue to serve as a technical subject matter expert as needed.

Portfolio Health, Strategy & Innovation

  • Ensure the long-term vitality of the IP&SS new product portfolio through disciplined execution, technical rigor, and strategic foresight.
  • Define and advance product and technology strategies that sustain competitive portfolios and incorporate feature, process, and technology improvements aligned to unmet customer and clinical needs.
  • Contribute to organic ideation, feasibility studies, and early technology exploration.
  • Support evaluation and due diligence activities for inorganic growth opportunities.

People Leadership & Culture

  • Establish and communicate a clear vision, culture, and development focus for the team.
  • Lead with a hands-on, player‑coach mindset, modeling accountability, technical excellence, and collaboration.
  • Strengthen medical device design rigor while empowering teams, increasing engagement, and fostering ownership.
  • Lead experienced professionals and specialists who operate with significant autonomy and technical judgment.

Your Skills and Expertise To set you up for success in this role from day one, Solventum requires (at a minimum) the following qualifications:

  • Bachelors Degree in an applicable technical field
  • Ten years of relevant experience
  • Experience in a regulated industry (medical devices preferred) utilizing design controls to design, develop, verify, validate, and commercialize new products
  • Previous experience managing people, leading teams, and developing/managing budgets

In addition to the above requirements, the following are also required:

  • Expertise in project technical leadership with the ability to oversee multiple…
Position Requirements
10+ Years work experience
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