Jobs at Imperative Care

Lead and execute software programs for a robotic medical device from concept through release and transfer to manufacturing. Own release cadence, lifecycle documentation, requirements traceability, defect triage, and regulatory audit-readiness per IEC 62304. Coordinate cross-functional teams, automate CI/CD workflows, and improve release predictability and compliance.

The Sr Cost Accountant will manage inventory and cost accounting, ensuring accuracy and implementing process improvements while collaborating with various teams for better visibility into costs and margins.

Lead the quality assurance function for robotics medical devices: build and maintain the QMS, ensure compliance with FDA and international standards, define regulatory strategy, oversee verification/validation and supplier quality, and grow/manage the QA team to support product transfer to manufacturing and commercial launch.

Lead commercial analytics, reporting, and decision support for Sales. Build dashboards, forecast models, and BI solutions (Salesforce, Tableau/Power BI, SQL, Snowflake). Provide executive insights, territory and quota analytics, pipeline and performance analysis, and mentor analysts while ensuring data governance and cross-functional alignment.

The Director of Product Management will lead marketing efforts for the peripheral vascular portfolio, manage product lifecycles, and develop strategies for market growth and team development.

Design, implement, and test hard real-time algorithms, state machines, and application logic for a robotic medical platform. Develop C++/Python production code on Linux and RTOS, collaborate with cross-functional teams, contribute to testing and simulation environments, participate in design reviews, and ensure safety-critical software quality.

The Staff Software Test Engineer designs and executes test procedures for robotic medical software, ensuring compliance with regulatory standards and quality requirements.

Lead sterilization, microbiology and biocompatibility quality activities across product development and manufacturing. Develop and execute quality plans, risk management, validations, supplier qualifications and audits. Oversee testing labs, analyze results, manage CAPAs/NCMRs, prepare regulatory submissions, and provide training and QA system compliance for medical device products.

Assist early‑phase design and development of endovascular interventional medical devices. Support prototyping, testing, statistical analysis, design documentation, specification setting, design verification, and validation activities while collaborating with technicians and senior engineers.

Designs and implements repeatable test methods, fixtures, and automation to characterize and verify medical device performance. Performs experimental design, statistical analysis (gage R&R, DOE), test method validation, and collaborates with design and preclinical teams under regulated quality systems.

Lead process design and implementation of medical device production, ensuring effective methods and technologies are utilized for commercialization. Provide expertise and guidance on project management and compliance with quality systems.

The Principal R&D Engineer leads projects in catheter engineering, driving innovation, evaluating product designs, and mentoring team members. Responsibilities include ensuring manufacturability and compliance with quality systems.

The Sr Supplier Quality Engineer leads quality engineering support across medical device development and supplier performance improvements, ensuring compliance with regulations and driving supplier quality enhancements.

Manage supplier and contract manufacturing quality for medical device products; lead supplier audits, incoming inspection, SCAR/CAPA/NCR resolution, and supplier qualification. Oversee and mentor the Supplier Quality Engineering team, develop quality metrics, ensure ISO 13485/FDA compliance, and drive continuous improvement and risk management across suppliers and internal partners.

Lead design and development of endovascular/neurovascular products through concept, prototyping, verification/validation, and manufacturability assessments. Build catheter/controller prototypes, author drawings and test protocols, perform design control activities, risk analyses (FMEAs, Hazards), verification testing, and support design validation to ensure compliance with quality system requirements.

Lead and support lifecycle management of endovascular products, including design development, verification/validation, manufacturability assessments, prototyping, requirements/specifications, and testing. Investigate field issues and perform root-cause analysis. Collaborate cross-functionally, engage suppliers and manufacturing partners, refine designs from market feedback, and support commercialization, training, and supporting materials.

Lead design and lifecycle management of endovascular medical devices, driving design development, verification/validation, and manufacturability. Serve as R&D lead on cross-functional teams, mentor junior engineers, liaise with clinicians and regulatory, research vendors/materials, and ensure products meet quality, cost, schedule, and regulatory requirements.

The Sr Software Engineer will design and implement software applications and algorithms for robotic systems, ensuring reliability and scalability while collaborating with cross-functional teams in a medical context.

Lead preparation and review of public company SEC filings (10-K, 10-Q, 8-K), manage technical accounting (leases, revenue, ASC 718, business combinations), oversee stock-based compensation reporting, support month/quarter close and SOX compliance, coordinate with auditors and cross-functional teams, and maintain disclosure controls and accounting documentation.