The Senior Manager will lead global value-based market access strategies for URO/GYN business units, focusing on balloon rectal spacers. They will drive evidence generation, manage reimbursement projects, and ensure economic value propositions meet the needs of global stakeholders.
The Principal Quality Engineer serves as the primary point of contact for end-to-end product quality, ensuring compliance with regulatory standards and internal requirements. This role leads cross-functional teams to resolve product quality issues, manage CAPA processes, and oversee risk management and design transfer activities.
The Service Sales Executive is responsible for managing, protecting, and growing the service contract portfolio for the Medical Systems Group within Indiana and Wisconsin. They will drive revenue growth, conduct executive-level business reviews, and collaborate with cross-functional teams to deliver value-based solutions to IDNs and GPOs.
The Software Implementation Engineer II manages the end-to-end installation of medical software, coordinating with hospital IT teams and internal stakeholders to ensure successful deployment. They also provide technical sales support, conduct product demonstrations, and perform site surveys to assess customer needs and optimize system requirements.
The Solutions Sales Manager is responsible for driving regional revenue growth for the OLYSENSE digital and AI-powered endoscopy platform through competitive displacement and account expansion. This role involves executing territory strategies, managing complex multi-stakeholder sales cycles, and ensuring successful customer adoption and integration.
The Director of Clinical Research leads the development and execution of global evidence generation strategies for the URO portfolio to support regulatory, commercial, and market access objectives. This role provides scientific leadership, manages cross-functional clinical initiatives, and fosters relationships with key opinion leaders and internal stakeholders.
This role serves as the Voice of Quality on cross-functional new product development teams, establishing quality and reliability strategies. The manager oversees project quality initiatives, ensures compliance with quality systems, and drives risk management and corrective actions.
This role oversees clinical trial activities at study sites, ensuring high-quality execution, regulatory compliance, and the achievement of enrollment goals. The manager acts as the primary liaison between the company and clinical sites to drive performance and mitigate operational risks.
Develop and execute a global strategy for post-market monitoring by integrating internal quality data with external market intelligence and AI-enabled analytics. Lead a high-performing team to identify emerging risks and safety signals to improve product performance and regulatory compliance.
The Director, BD Regulatory Affairs is responsible for strategic and tactical support for business development projects, serving as a liaison between Regulatory Affairs and the Business Development team. This role includes developing regulatory pathways, maintaining regulatory documentation, and ensuring compliance with global regulatory requirements.
Responsible for the end-to-end delivery of tech-enabled change projects, managing the full lifecycle from analysis to deployment. This includes owning project plans, financials, and resource models while ensuring robust governance and stakeholder communication.
Drive product quality and patient safety by leading CAPA efforts and coaching site leads in technical problem-solving methods. Oversee Design Assurance training and support high-priority complaint investigations and new product development.
Oversee the operational execution of large-scale, complex clinical trials, managing timelines, budgets, and vendors. Provide people leadership and mentorship to Clinical Project Management staff while coordinating cross-functional study teams.
