Jobs at Solventum

Lead enterprise data strategy and governance: define strategy, design governance frameworks (ownership, stewardship, quality, standards), partner on scalable cloud/MDM/metadata/analytics platforms, establish governance forums, and drive cross-functional change to embed trusted, data-driven decision-making.

Design, build, and deploy enterprise-scale agentic and generative AI systems for healthcare. Architect multi-agent frameworks, implement advanced RAG and multimodal data pipelines, optimize LLM performance and latency, establish MLOps/CI-CD and secure containerized deployments, and collaborate with stakeholders to ensure clinical safety and compliance (HIPAA/HITRUST). Mentor developers and produce production-grade documentation.

Design, implement, and evaluate advanced NLP/NLU systems for clinical text using transformer and research-oriented neural architectures. Prepare and enrich clinical datasets, run experiments and error analyses, mitigate model risks (bias, drift, hallucination), and partner with ML engineers to deploy models into a compliant cloud environment.

Build and maintain MLOps pipelines, deploy and monitor ML models as scalable services, transform and integrate healthcare data (FHIR/HL7), ensure reproducible feature management, and uphold HIPAA/HITRUST security for production ML in clinical systems.

As a Scientific Education Manager, you will coordinate and execute educational workshops, manage event logistics, and support clinical education initiatives while collaborating with healthcare professionals.

The role involves developing NLP systems for medical document analysis using advanced deep learning techniques, collaborating with domain experts, and deploying models in a healthcare setting.

Lead development and maintenance of inpatient analytics content by collaborating with CDI, coding, clinical, BI, and UX teams. Define KPIs, present dashboards to stakeholders, contribute to content roadmap, ensure compliance with quality and security standards, and support corporate initiatives.

In this role, you will manage systems engineering processes, define system architecture, ensure compliance with regulations, and collaborate across various engineering teams to develop medical devices, guiding the technical team through system design and validation.

Lead commercial, strategic and tactical management of electronics components and contract manufacturers to ensure product availability. Develop supplier relationships, negotiate contracts, run RFPs/RFQs, perform cost and risk analyses, support NPI, and partner cross-functionally to improve supply chain performance, cost, quality, and lead times.

Review inpatient records to ensure accurate, complete clinical documentation for SOI, ROM, quality outcomes, medical necessity, and reimbursement. Perform concurrent/retrospective reviews, initiate physician queries, collaborate with coding staff, monitor documentation trends, conduct clinical validation for high-risk diagnoses, participate in rounds and education, and support denial prevention and documentation improvement initiatives.

Lead preparation and submission of 510(k) and other regulatory filings for SaMD. Develop and execute global regulatory strategies (US, EU MDR, Canada), review technical/software documentation, ensure regulatory compliance, and collaborate cross-functionally to integrate requirements into product development.

Lead design and delivery of enterprise BI and analytics solutions for healthcare coding and clinical data. Define BI architecture, data models, ETL pipelines, cloud-native analytics, and implement agentic/generative AI analytics for global customers while guiding engineering best practices and mentoring teams.

Regional EHS Manager responsible for establishing and implementing EHS governance, programs and compliance across manufacturing and non-manufacturing sites in the Americas. Lead SIF prevention, incident investigations, audits, regulatory analysis, self-assessments, improvement plans, and acquisition due diligence while supporting site EHS leaders and deploying global EHS policies and management systems.

As a Technical Architect, you'll lead solution evaluation, define architecture strategy, guide cloud modernization, and embed security compliance, collaborating with teams and vendors.

Lead and technically supervise cross-functional Agile teams building and rearchitecting HIS software products. Hire, mentor, set technical direction, prioritize backlogs, drive CI/CD and quality, coordinate with product and business stakeholders, and champion Agile practices to deliver cloud and on-premises solutions that improve healthcare outcomes.

The Senior Managing Counsel will provide legal support for privacy and cybersecurity, ensuring compliance with laws and assessing risks related to data security. This role involves collaboration with IT and business teams to enhance security posture and manage legal obligations effectively.

As a Clinical Analyst, you will utilize nursing knowledge to analyze clinical data, support product development with NLP, and coordinate content usage across departments.

The Senior Manager will lead a team in Clinical Engineering and Data Analytics, focusing on AI-driven clinical outcomes and strategic direction for healthcare solutions in dental solutions.

The Assistant Chief IP Counsel will provide strategic IP guidance, manage patents, oversee IP disputes, and support business growth through legal expertise in a global healthcare company.

The Principal Regulatory Affairs Specialist will lead regulatory submissions and strategies for dental products, ensuring compliance globally and driving improvements in regulatory processes.