The Solutions Sales Manager is responsible for driving regional growth of the OLYSENSE digital and AI-powered endoscopy platform through competitive displacement and account expansion. This role involves leading end-to-end deal execution, managing a robust sales pipeline, and engaging with clinical, administrative, and hospital IT stakeholders.
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.
The Global Lead provides expert medical and clinical guidance to shape the Gastroenterology EndoTherapy strategy across the product lifecycle. They engage with internal and external stakeholders, including physicians and payors, to ensure clinical impact and patient-centric care.
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.
This role assists in the development and execution of clinical evidence generation strategies and clinical study activities for the Gastrointestinal Solutions Division. Responsibilities include writing study protocols, managing regulatory submissions, and collaborating with cross-functional teams to support product commercialization.
The Senior Director is responsible for developing and executing regional professional education strategies and training plans for healthcare professionals. They lead cross-functional collaboration to ensure safe and effective product use while managing budgets and performance metrics.
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.
Lead the development and completion of data-driven Health Hazard Assessments (HHAs) globally to ensure safety and compliance. Manage project teams, present findings to review boards, and collaborate with legal and compliance departments.
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.
Serve as the primary point of contact for end-to-end product quality, ensuring compliance with regulatory standards across the product lifecycle. Lead CAPA processes, risk management activities, and cross-functional teams to resolve product and process deficiencies.
Lead and influence global medical safety activities, focusing on the detection, assessment, and mitigation of product risks to protect patients. Collaborate cross-functionally to provide medical safety reviews for regulatory documentation, CAPAs, and post-market surveillance.
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.
The Senior Director leads the global endoscopic reprocessing innovation portfolio, defining long-term product vision and managing the innovation roadmap from concept to market. They are responsible for leading a team of product managers and driving cross-functional collaboration to ensure the delivery of high-value, compliant medical solutions.
