Serve as the interface between the market (the voice of the customer) and Magenta’s R&D organization. Help define product roadmaps, including requirements, specifications, risks, hazards, pre-clinical testing, and go-to-market activities.
What you'll do
Lead usability testing activities, lead product training efforts.
Participate in marketing activities related to the product.
Gather needs for current and future products, identify optimized solutions, lead strategic & tactical product roadmaps.
Own and responsible for full product lifecycle.
Responsible for characterization of new products and features.
Responsible to monitor competitive activity, ranging from IP, through technical features, to market performance and marketing activities.
Provide input to product training and marketing activities/materials.
Provide support for products that are sold in mass numbers, interface with sales reps, distributors, and end-customers worldwide.
Requirements
M.Sc. in a relevant field.
Desirable to have at least 8 years of experience in product management (preferably B2B) or shorter R&D experience.
Experience with FDA submissions and FDA human factors/usability studies.
Experience defining user interfaces, product requirements, product specifications, and hazard analyses.
Experience presenting scientific and clinical data before advisory boards.
Advantages to experience in adjacent disciplines/roles, such as: Product Marketing / Marketing / Business Development / R&D Developer / Team Leader / Program Management / Project Management.
Thorough understanding of organizational processes - experience working with internal stakeholders from product definition to launch.
Nice to have
English - full proficiency. Native speaker - an advantage.
Excellent verbal and writing skills.
High capacity and motivation for self-learning.
Relevant M.A. and/or M.B.A. - an
Ph.D. or MD - an
Experience with sophisticated, data-rich products with a significant customer base, products or systems that combine hardware and software - an
Strong experience with cardiovascular or structural heart devices
Experience with Class III medical devices and pre-commercial stage companies - an