The Manager, OTTAVA Communications will develop strategic communication programs for surgical robotics and digital surgery, focusing on messaging, content creation, and campaign activation within a collaborative environment.

The Oncology Clinical Educator will provide education for Oncology brands to patient care teams, focusing on treatment and disease management for solid tumors. Responsibilities include developing territory plans, conducting presentations, and educating both healthcare providers and patients about clinical and operational aspects of oncology care.

Lead US clinical marketing strategy and enablement for Ottava Bariatrics & Foregut. Translate clinical insights into Challenger-based narratives, physician education, sales tools, and hospital adoption programs. Drive early hospital success, KOL engagement, conference strategy, and cross-functional alignment to accelerate specialty adoption and sustained utilization of the Ottava Surgical System.

Lead Environmental, Health & Safety compliance programs, ensure high EHS performance, provide technical expertise, and conduct assessments and training for safety culture.

Lead and scale a global connectivity operating model for medical devices, ensuring secure, reliable device-to-network-to-cloud connections. Drive governance, incident response, technical design authority, vendor management, and build a global team to enable standardized, repeatable deployments and measurable performance.

The NPI Manufacturing Engineer will lead new product introductions for robotic medical devices, focusing on manufacturing readiness, process optimization, and cross-functional collaboration to ensure quality and efficiency in production.

The Sr. Marketing Manager will lead strategic initiatives, coordinate cross-functional teams, compile analyses, and manage key projects to support the OTTAVA Operating Committee's goals in enhancing surgical care innovations.

The Territory Manager is responsible for expanding sales of Johnson & Johnson products, managing accounts, building relationships with physicians, and executing a professional sales cycle.

Lead a team focused on hardware reliability for robotic systems, defining strategies, managing projects, and ensuring compliance with medical device regulations.

The Manufacturing Test Engineer designs, develops, and qualifies test software for manufacturing medical robotics systems, performs debugging, and ensures regulatory compliance.

The Director Clinical Science leads clinical studies design and execution, ensuring compliance and patient safety while overseeing regulatory communication and team mentoring.

The Associate Clinical Account Specialist provides clinical product and technical support in electrophysiology labs, engaging with various stakeholders and exceeding business goals after training.

The Principal Clinical Research Scientist leads clinical programs in ophthalmic device research, collaborates with cross-functional teams, and engages with regulatory agencies to drive product innovation.

Lead and execute medical device clinical trials including site management, monitoring, document development, data review, regulatory compliance (ICH-GCP/SOPs), vendor coordination, and reporting, ensuring timelines, inspection readiness, and cross-functional collaboration.

The Senior Technical Sales Specialist will lead technical sales engagements for connected medical devices, provide customer support, and collaborate with sales teams to enhance strategy and product knowledge.

Lead global communications for the Monarch surgical robotics platform and Polyphonic digital ecosystem. Advise senior leaders, build integrated communications plans, manage teams and agencies, drive media relations, content strategy, digital/social and brand-aligned campaigns to support commercial and product goals.

The Staff Microbiology Specialist ensures quality assurance in microbiology for medical devices, leading design control activities and compliance with standards and regulations.

The Associate Clinical Account Specialist trains for up to 9 months to provide technical product assistance in electrophysiology sales, focusing on improving cardiovascular patient care.

The Director, Bioresearch Quality Process Management oversees quality process enhancements in Bioresearch, ensuring compliance with regulations and driving risk management and continuous improvement across MedTech. This role includes leadership, stakeholder engagement, and data analytics.

As a Software Engineer in the Simulation team, you will develop advanced training simulator software for medical robots, collaborating with cross-functional teams to drive software design and architecture.