Cascadia Search Group
Executive Director, Product & Technology Development
Cascadia Search Group, Nashville, Tennessee, United States, 37247
The Executive Director, Product & Technology Development, is a senior leader within the R&D organization responsible for shaping and executing the company's product, technology and innovation roadmap. This role will lead end-to-end product lifecycle management, from concept through commercialization and will lead engineering & technology teams focused on delivering breakthrough solutions in the life sciences & technology space. The ideal candidate combines Leadership, strategic vision, technical expertise, and a passion for innovation to ensure our product portfolio & innovation team remains competitive, customer-focused, forward-thinking & future ready. This role reports to the Chief Innovation Officer.
Education:
Bachelor's degree in engineering, Biomedical Sciences, or a related field (Master's or Ph.D. preferred). Experience:
12+ years of experience in medical device product development, with at least 5 years in leadership roles. Demonstrated success in developing & launching class II/III FDA-regulated medical devices as well as EU MDR environment. Experience managing global teams a plus. Skills & Competencies:
In-depth knowledge of design controls (ISO 13485), DHF, risk management and usability engineering. Strong leadership, communication, and stakeholder management skills. Strategic thinker with hands-on execution capabilities. PMP certification or experience in structured project management methodologies is highly desired. Define and execute the product development strategy aligned with company goals and market needs. Collaborate with executive leadership to establish the product roadmap and innovation pipeline. Lead the development lifecycle of Class II/III medical devices, including concept, design, development, verification/validation, and transfer to manufacturing. Oversee design control processes in compliance with FDA 21 CFR Part 820, ISO 13485, and other applicable regulations. Foster a culture of design excellence, design reliability/risk management, and continuous improvement. Build, mentor, and lead a high-performing multi-disciplinary team, including engineers, program managers, and scientists. Drive performance through clear objectives, accountability, and professional development. Partner with Regulatory Affairs, Quality Assurance, Clinical, Marketing, and Operations to align development activities with business and compliance requirements. Ensure effective design transfer and scale-up into manufacturing. Monitor emerging technologies, market trends, and competitive landscape to identify innovation opportunities. Engage with key opinion leaders (KOLs), customers, and stakeholders to translate clinical needs into product solutions. Competitive salary and benefits package Opportunities for professional development and career growth. Collaborative and innovative work environment.
Working Conditions: Office based role in Nashville/Franklin TN area
Travel Expectations: 30%
Education:
Bachelor's degree in engineering, Biomedical Sciences, or a related field (Master's or Ph.D. preferred). Experience:
12+ years of experience in medical device product development, with at least 5 years in leadership roles. Demonstrated success in developing & launching class II/III FDA-regulated medical devices as well as EU MDR environment. Experience managing global teams a plus. Skills & Competencies:
In-depth knowledge of design controls (ISO 13485), DHF, risk management and usability engineering. Strong leadership, communication, and stakeholder management skills. Strategic thinker with hands-on execution capabilities. PMP certification or experience in structured project management methodologies is highly desired. Define and execute the product development strategy aligned with company goals and market needs. Collaborate with executive leadership to establish the product roadmap and innovation pipeline. Lead the development lifecycle of Class II/III medical devices, including concept, design, development, verification/validation, and transfer to manufacturing. Oversee design control processes in compliance with FDA 21 CFR Part 820, ISO 13485, and other applicable regulations. Foster a culture of design excellence, design reliability/risk management, and continuous improvement. Build, mentor, and lead a high-performing multi-disciplinary team, including engineers, program managers, and scientists. Drive performance through clear objectives, accountability, and professional development. Partner with Regulatory Affairs, Quality Assurance, Clinical, Marketing, and Operations to align development activities with business and compliance requirements. Ensure effective design transfer and scale-up into manufacturing. Monitor emerging technologies, market trends, and competitive landscape to identify innovation opportunities. Engage with key opinion leaders (KOLs), customers, and stakeholders to translate clinical needs into product solutions. Competitive salary and benefits package Opportunities for professional development and career growth. Collaborative and innovative work environment.
Working Conditions: Office based role in Nashville/Franklin TN area
Travel Expectations: 30%