Jobs at Imperative Care

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 Design Assurance for medical device product development and lifecycle activities. Establish processes, drive Design Controls, risk management, V&V, usability, and design transfer. Provide cross-functional quality leadership, mentor staff, support audits/inspections, and improve product reliability and development effectiveness.

The Sr Executive Assistant provides administrative support to executive leaders, coordinates travel and meetings, manages information flow, and maintains organized documents and records with confidentiality.

Lead and manage R&D teams to deliver medical device product development from concept through transfer to manufacturing. Set strategy, budgets, timelines, and resources; drive prototyping, design improvements, and regulatory design control. Collaborate cross-functionally and with external partners, mentor staff, resolve technical issues, and represent R&D in clinical, regulatory, and business discussions. Attend professional meetings and support filing and qualification activities.

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.

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 Senior Commercial Excellence Manager drives revenue growth and sales force effectiveness by optimizing commercial infrastructure and supporting sales strategy, forecasting, and compensation planning.

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.

The Sr Data Analytics & Business Insights Manager leads analytics capabilities, defines KPIs, develops predictive models, and ensures metric integrity across the organization while collaborating with multiple departments.

The Sr R&D Engineer will design and develop innovative neurovascular products, conduct risk analyses, and ensure adherence to quality standards while leading various product development activities.

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 R&D Engineer leads the design and development of new endovascular/neurovascular products, guiding cross-functional teams, conducting research, and ensuring manufacturability while meeting performance and cost targets.

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.

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

The Sr Process Development Engineer will define, optimize, and validate manufacturing processes for neuro-interventional medical devices, while collaborating with cross-functional teams to improve equipment and document processes.

Develop and test software applications for robotic-assisted technologies in healthcare. Collaborate with cross-functional teams, focusing on UI design, user requirements, and software architecture.

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.

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.