Leads platform and software product portfolio planning and requirements definition, establishing clear direction on intended use claims, workflows, value propositions, and success metrics to support timely decisions.
Leads product development, launch, and lifecycle management, partnering with R&D, Medical Affairs, Regulatory, Quality, and Operations while evaluating products, extensions, and partnerships through value, evidence needs, regulatory pathways, and market access considerations to ensure compliance and differentiation.
Translates evolving clinical practices and guidelines into clear roadmap priorities and portfolio decisions, acting as a strategic thought partner with Medical and Regulatory Affairs.
Leads launch and market activation, ensuring coordination, supply readiness, and clinical and scientific messaging and guiding development of sales enablement tools, ensuring accurate, and compelling product positioning.
Champions customer and market insights, integrating clinician input, laboratory feedback, KOL engagement, and market intelligence to guide portfolio direction and market impact.
Serves as the primary product interface across global functions and regions, balancing global alignment with local clinical practice and regulatory needs.
Leads all aspects of portfolio performance and optimization, utilization, and feedback to identify risks and improvement opportunities.
Provides financial and pricing oversight, including revenue growth, margin improvement, pricing execution, and investment efficiency through evidence‑based value strategies.
Leads forecasting and supply planning, conducting business reviews to ensure supply continuity, performance optimization, and strategic alignment.
Requirements
Minimum of a bachelor’s degree in Biological Sciences, Engineering, Software or equivalent experience is required.
Advanced degree and/or MBA with equivalent experience also preferred.
Minimum of 5 years of product management experience within IVD, medical devices, or life sciences.
Experience in the development and commercialization of life science, diagnostic products or medical devices.
Broad technical experience consistent with the molecular diagnostic market.
Proven track record to lead cross-functional teams.
A strong record-building alignment in cross-functional teams and navigating within a matrix organization to achieve goals.