Global Corrective and Preventive; CAPA) Quality Analyst; Solventum
Listed on 2026-09-28
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Quality Assurance - QA/QC
Data Analyst, Regulatory Compliance Specialist
At Solventum, we improve lives by helping healthcare professionals do their best work. Join a team using innovation and insight to make a real impact on the future of healthcare. All roles listed are with Solventum, and we're committed to protecting your personal information—learn more in our Privacy Policy:
Job Description Global Corrective and Preventive (CAPA) Quality Analyst (Solventum) 3M Health Care is now SolventumAt 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 RoleAs a Global Corrective and Preventive (CAPA) Quality Analyst 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:
- Serving as a subject matter expert and coach for Corrective and Preventive Action (CAPA) requirements, methodologies, and processes.
- Conducting independent reviews of CAPA records and providing feedback to improve investigation quality, root cause analysis, corrective actions, and overall compliance.
- Supporting global CAPA governance activities, including CAPA Review Boards, escalation processes, and risk-based decision making.
- Developing and delivering training, coaching, guidance documents, and best-practice resources to strengthen CAPA knowledge and capability across the organization.
- Monitoring, analyzing, and reporting CAPA metrics and trends to identify opportunities for continuous improvement and support management review activities.
- Supporting deployment, adoption, and continuous improvement of QMS processes, systems, tools, and metrics across global sites.
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 AND four (4) years of previous experience in quality processes involving investigations, problem solving, and project management.
OR
- High School Diploma/GED AND eight (8) years of previous experience in quality processes involving investigations, problem solving, and project management.
Additional qualifications that could help you succeed even further in this role include:
- Understanding of domestic and international quality and auditing requirements, including ISO 13485, ISO 19011, FDA Quality System Regulations, CMDR, and EU MDR.
- Knowledge of CAPA governance, facilitating investigations, leading problem-solving activities, and coaching stakeholders through corrective and preventive action processes.
- Strong technical writing, analytical thinking, communication, problem-solving, and investigation skills, including experience with root cause analysis and quality improvement methodologies.
- Demonstrated ability to collaborate effectively across functions, cultures, and global locations while building strong stakeholder relationships.
- Ability to develop and deliver training, guidance materials, and presentations to diverse global audiences.
- Remote- USA
Travel:
May include up to 25% domestic or international
Relocation Assistance:
No
Must be legally authorized to work in…
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