Jobs at Integra LifeSciences

Senior commercial leader responsible for US marketing strategy and team leadership across ENT and Instruments. Drive product commercialization, launches, sales alignment, market development, KOL engagement, analytics-driven performance, compliance with FDA, and cross-functional collaboration to deliver revenue and market share growth.

Lead a medical device manufacturing site overseeing safety, quality, manufacturing, supply chain, engineering, facilities, and finance. Serve as Value Stream Manager driving continuous improvement, regulatory compliance (FDA, ISO 13485, EU MDR, CMDR), KPI performance (safety, quality, delivery, cost), budget management, and cross-functional alignment to meet productivity and capacity goals.

Design and develop ENT medical devices and accessories, create prototypes, tools, and test methods, execute V&V and pre-clinical studies, collaborate with vendors and cross-functional teams, ensure regulatory and quality compliance, and communicate project status and risks.

Provide sterility assurance expertise across manufacturing, regulatory, and quality functions. Maintain sterilization and contamination-control programs, perform validations and audits, support EU MDR and FDA compliance, assess contract sterilizers, train staff, and author validation protocols, SOPs, and reports to ensure regulatory and technical compliance.

Lead and develop global quality microbiology teams to ensure compliant microbiology programs across manufacturing sites. Oversee environmental and water system monitoring, endotoxin and bioburden test validation, contamination control, audits/inspections, cross-functional collaboration, and strategic microbiology process ownership to support manufacturing transfers, new products, and regulatory compliance.

Lead hands-on Oracle EBS finance and cost accounting functional work: configure and support GL/AP/AR/FA/SLA, manage costing and reconciliations, gather requirements, produce functional specs, support testing and integrations, resolve production issues, and drive process and reporting improvements across Record-to-Report.

Lead full-lifecycle design and development of ENT medical devices, manage vendor interactions, create prototypes, develop tests and protocols (V&V, pre-clinical, usability), gather VOC, lead technical reviews, ensure regulatory compliance, and communicate project status to management.

Lead functional design, configuration, testing, and post-implementation support for Oracle ASCP and Cloud Demand/Supply Planning. Drive requirements gathering, fit-gap analysis, integrations, reporting, validation for life-sciences clients, and deliver training and change management.

Lead hands-on Oracle EBS finance and cost accounting functional work across Record-to-Report. Configure and support GL/AP/AR/FA/SLA and costing, perform reconciliations, drive period close, create functional specs, support testing and integrations, analyze production issues, and identify process and reporting improvements to ensure accurate close, controls, and compliance in a regulated environment.

Support and optimize medical device manufacturing processes using lean and Six Sigma methods. Execute validations (IQ/OQ/PQ/TMV), statistical process control, FMEA/CAPA investigations, engineering change management, and cross-functional projects to improve yield, quality, cost, and process documentation while ensuring regulatory compliance (FDA, GMP, ISO 13485).