Solventum

Morden
6,539 Total Employees

Jobs at Solventum

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Recently posted jobs

YesterdaySaved
In-Office or Remote
3 Locations
Healthtech • Pharmaceutical • Manufacturing
Serves as a Canadian healthcare workflow and product subject matter expert for 360 Encompass implementations, adoption, and optimization. Advises customers on coding, CDI, data quality, reporting, and operational workflows; supports configuration, change management, training, demonstrations, and readiness activities. Leads workflow design and post-go-live optimization, while providing adoption metrics, reporting insights, best practices, and executive communication. Requires Canadian HIM certification, substantial healthcare experience, and customer-facing implementation or advisory expertise.
6 Days AgoSaved
Remote
3 Locations
Healthtech • Pharmaceutical • Manufacturing
Implement healthcare information systems for Canadian healthcare customers. Responsibilities include assessing and validating coding, abstracting, CDI, and HIM workflows; configuring, testing, and supporting application environments; investigating issues; documenting risks; coordinating customer communications; supporting go-live readiness; and training administrators, super users, and end users.
15 Days AgoSaved
Remote
Canada
Healthtech • Pharmaceutical • Manufacturing
Drives adoption and optimization of Solventum clinician productivity solutions for Canadian healthcare customers. Assesses clinician workflows, develops adoption plans and success metrics, delivers training and readiness sessions, monitors utilization, removes adoption barriers, and recommends improvements. Serves as a trusted advisor to clinical, operational, and IT stakeholders while partnering with product and development teams on customer feedback. Supports change management, workflow optimization, post-go-live reviews, and continuous improvement of customer success and implementation programs.
28 Days AgoSaved
Remote or Hybrid
3 Locations
Healthtech • Pharmaceutical • Manufacturing
Leads systems engineering for regulated, embedded electro-mechanical medical devices. Responsibilities include requirements engineering, system architecture, risk management, integration, verification and validation, technical reviews, cross-functional design resolution, and regulatory documentation for FDA and EU submissions. The role provides technical leadership across mechanical, electrical, software, and quality teams while evaluating system alternatives, managing product documentation, and mitigating technical risks.